RSS-Feed abonnieren
DOI: 10.1055/a-2029-0134
Prävention, Diagnostik, Therapie und Nachsorge des Lungenkarzinoms
Interdisziplinäre S3-Leitlinie der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin und der Deutschen Krebsgesellschaft – KurzfassungPrevention, Diagnosis, Therapy, and Follow-up of Lung CancerInterdisciplinary Guideline of the German Respiratory Society and the German Cancer Society – Abridged VersionZusammenfassung
Die aktuelle Fassung der Leitlinie Lungenkarzinom trägt der Dynamik der Informationen in diesem Fachbereich Rechnung. Insbesondere gelten folgenden Empfehlungen:
Die Vorstellung aller neu diagnostizierten Patienten im interdisziplinären pneumoonkologischen Tumorboard ist verpflichtend, das CT-Screening für asymptomatische Risikopersonen (nach Zulassung durch die Behörden), Vorgehen beim inzidentellen Lungenrundherd (außerhalb von Screeningprogrammen), molekulare Testung aller NSCLC unabhängig vom Subtyp, in frühen Stadien auf EGFR-Mutationen und in der Rezidivsituation, adjuvante TKI-Therapie bei Vorliegen einer EGFR-Mutation, adjuvante Konsolidierung mit Checkpointinhibitor bei PD-L1 ≥ 50%, Erhebung des PD-L1-Status, nach Radiochemotherapie bei PD-L1-pos. Tumoren Konsolidierung mit Checkpointinhibitor, adjuvante Konsolidierung mit Checkpointinhibitor bei PD-L1 ≥ 50% im Stadium IIIA, Erweiterung des therapeutischen Spektrums bei PD-L1 ≥ 50%, unabhängig von PD-L1Status, neue zielgerichtete Therapieoptionen sowie die Einführung der Immunchemotherapie in der SCLC Erstlinie.
Um eine zeitnahe Umsetzung künftiger Neuerungen zu gewährleisten, wurde die Umstellung auf eine „living guideline“ für das Lungenkarzinom befürwortet.
Abstract
The current S3 Lung Cancer Guidelines are edited with fundamental changes to the previous edition based on the dynamic influx of information to this field:
The recommendations include de novo a mandatory case presentation for all patients with lung cancer in a multidisciplinary tumor board before initiation of treatment, furthermore CT-Screening for asymptomatic patients at risk (after federal approval), recommendations for incidental lung nodule management , molecular testing of all NSCLC independent of subtypes, EGFR-mutations in resectable early stage lung cancer in relapsed or recurrent disease, adjuvant TKI-therapy in the presence of common EGFR-mutations, adjuvant consolidation treatment with checkpoint inhibitors in resected lung cancer with PD-L1 ≥ 50%, obligatory evaluation of PD-L1-status, consolidation treatment with checkpoint inhibition after radiochemotherapy in patients with PD-L1-pos. tumor, adjuvant consolidation treatment with checkpoint inhibition in patients withPD-L1 ≥ 50% stage IIIA and treatment options in PD-L1 ≥ 50% tumors independent of PD-L1status and targeted therapy and treatment option immune chemotherapy in first line SCLC patients.
Based on the current dynamic status of information in this field and the turnaround time required to implement new options, a transformation to a „living guideline“ was proposed.
Publikationsverlauf
Artikel online veröffentlicht:
26. Oktober 2023
© 2023. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
Literatur
- 1 Barta JA, Powell CA, Wisnivesky JP. Global Epidemiology of Lung Cancer. Ann Glob Health 2019; 85 DOI: 10.5334/aogh.2419. https://www.ncbi.nlm.nih.gov/pubmed/30741509
- 2 Wild C, Weiderpass E, Stewart BW. International Agency for Research on Cancer WHO. World cancer report cancer research for cancer prevention. 2020
- 3 Barnes B, Kraywinkel K, Nowossadeck E. et al. Bericht zum Krebsgeschehen in Deutschland 2016. 2016
- 4 Hoebel J, Kroll L, Fiebig J. et al. Socioeconomic Inequalities in Total and Site-Specific Cancer Incidence in Germany: A Population-Based Registry Study. Front Oncol 2018; 8: 402 https://pubmed.ncbi.nlm.nih.gov/30319967/
- 5 Sidorchuk A, Agardh E, Aremu O. et al. Socioeconomic differences in lung cancer incidence: a systematic review and meta-analysis. Cancer Causes Control 2009; 20: 459-471 https://pubmed.ncbi.nlm.nih.gov/19184626/
- 6 Geyer S. Social inequalities in the incidence and case fatality of cancers of the lung, the stomach, the bowels, and the breast. Cancer Causes Control 2008; 19: 965-974 https://pubmed.ncbi.nlm.nih.gov/18431680/
- 7 Kuznetsov L, Mielck A. [Regional concentration of social disadvantage and of risks for lung cancer and colon cancer: systematic review and recommendations for research]. Gesundheitswesen 2012; 74: e42-e51
- 8 Van der Heyden JH, Schaap MM, Kunst AE. et al. Socioeconomic inequalities in lung cancer mortality in 16 European populations. Lung Cancer 2009; 63: 322-330 https://www.ncbi.nlm.nih.gov/pubmed/18656277
- 9 Menvielle G, Boshuizen H, Kunst A. et al. The role of smoking and diet in explaining educational inequalities in lung cancer incidence. J Natl Cancer Inst 2009; 101: 321-330 https://pubmed.ncbi.nlm.nih.gov/19244178/
- 10 Hastert T, Ruterbusch J, Beresford S. et al. Contribution of health behaviors to the association between area-level socioeconomic status and cancer mortality. Soc Sci Med 2016; 148: 52-58 https://pubmed.ncbi.nlm.nih.gov/26650930/
- 11 Finke I, Behrens G, Weisser L. et al. Socioeconomic Differences and Lung Cancer Survival-Systematic Review and Meta-Analysis. Front Oncol 2018; 8: 536 https://pubmed.ncbi.nlm.nih.gov/30542641/
- 12 Finke I, Behrens G, Maier W. et al. Small-area analysis on socioeconomic inequalities in cancer survival for 25 cancer sites in Germany. Int J Cancer 2021; 149: 561-572 https://pubmed.ncbi.nlm.nih.gov/33751564/
- 13 Wong M, Lao X, Ho K. et al. Incidence and mortality of lung cancer: global trends and association with socioeconomic status. Sci Rep 2017; 7: 14300 https://pubmed.ncbi.nlm.nih.gov/29085026/
- 14 Erdmann F, Spix C, Katalinic A. et al. Krebs in Deutschland für 2017/2018. 2021 http://dx.doi.org/10.25646/8353
- 15 Manser R, Lethaby A, Irving LB. et al. Screening for lung cancer. Cochrane Database Syst Rev 2013; 6: CD001991 https://www.ncbi.nlm.nih.gov/pubmed/23794187
- 16 Hunger T, Wanka-Pail E, Brix G. et al. Lung Cancer Screening with Low-Dose CT in Smokers: A Systematic Review and Meta-Analysis. Diagnostics (Basel) 2021; 11 DOI: 10.3390/diagnostics11061040. https://pubmed.ncbi.nlm.nih.gov/34198856/
- 17 Passiglia F, Cinquini M, Bertolaccini L. et al. Benefits and Harms of Lung Cancer Screening by Chest Computed Tomography: A Systematic Review and Meta-Analysis. J Clin Oncol 2021; 39: 2574-2585 https://pubmed.ncbi.nlm.nih.gov/34236916/
- 18 Lungenkrebsscreening mittels Niedrigdosis-Computertomografie Auftrag: S19-02 Version: 10, Stand: 19102020. IQWiG-Berichte – Nr. 982. 2020 https://www.iqwig.de/projekte/s19-02.html
- 19 Aberle DR, Adams AM, Berg CD. et al. Reduced lung-cancer mortality with low-dose computed tomographic screening. N Engl J Med 2011; 365: 395-409 https://www.ncbi.nlm.nih.gov/pubmed/21714641
- 20 Infante M, Cavuto S, Lutman FR. et al. A randomized study of lung cancer screening with spiral computed tomography: three-year results from the DANTE trial. Am J Respir Crit Care Med 2009; 180: 445-453 https://www.ncbi.nlm.nih.gov/pubmed/19520905
- 21 Infante M, Cavuto S, Lutman FR. et al. Long-Term Follow-up Results of the DANTE Trial, a Randomized Study of Lung Cancer Screening with Spiral Computed Tomography. Am J Respir Crit Care Med 2015; 191: 1166-1175 https://www.ncbi.nlm.nih.gov/pubmed/25760561
- 22 Pastorino U, Rossi M, Rosato V. et al. Annual or biennial CT screening versus observation in heavy smokers: 5-year results of the MILD trial. Eur J Cancer Prev 2012; 21: 308-315 https://www.ncbi.nlm.nih.gov/pubmed/22465911
- 23 Pastorino U, Silva M, Sestini S. et al. Prolonged lung cancer screening reduced 10-year mortality in the MILD trial: new confirmation of lung cancer screening efficacy. Ann Oncol 2019; 30: 1162-1169 https://pubmed.ncbi.nlm.nih.gov/30937431/
- 24 Saghir Z, Dirksen A, Ashraf H. et al. CT screening for lung cancer brings forward early disease The randomised Danish Lung Cancer Screening Trial: status after five annual screening rounds with low-dose CT. Thorax 2012; 67: 296-301 https://www.ncbi.nlm.nih.gov/pubmed/22286927
- 25 Wille MMW, Dirksen A, Ashraf H. et al. Results of the Randomized Danish Lung Cancer Screening Trial with Focus on High-Risk Profiling. Am J Respir Crit Care Med 2016; 193: 542-551
- 26 van den Bergh KA, Essink-Bot ML, Bunge EM. et al. Impact of computed tomography screening for lung cancer on participants in a randomized controlled trial (NELSON trial). Cancer 2008; 113: 396-404 https://www.ncbi.nlm.nih.gov/pubmed/18484588
- 27 van den Bergh KA, Essink-Bot ML, Borsboom GJ. et al. Short-term health-related quality of life consequences in a lung cancer CT screening trial (NELSON). Br J Cancer 2010; 102: 27-34 https://www.ncbi.nlm.nih.gov/pubmed/19935789
- 28 van den Bergh KA, Essink-Bot ML, Borsboom GJ. et al. Long-term effects of lung cancer computed tomography screening on health-related quality of life: the NELSON trial. Eur Respir J 2011; 38: 154-161 https://www.ncbi.nlm.nih.gov/pubmed/21148229
- 29 van de Wiel JC, Wang Y, Xu DM. et al. Neglectable benefit of searching for incidental findings in the Dutch-Belgian lung cancer screening trial (NELSON) using low-dose multidetector CT. Eur Radiol 2007; 17: 1474-1482 https://www.ncbi.nlm.nih.gov/pubmed/17206426
- 30 de Koning H, van der Aalst C, de Jong P. et al. Reduced Lung-Cancer Mortality with Volume CT Screening in a Randomized Trial. N Engl J Med 2020; 382: 503-513 https://pubmed.ncbi.nlm.nih.gov/31995683/
- 31 Becker N, Motsch E, Gross M-L. et al. Randomized Study on Early Detection of Lung Cancer with MSCT in Germany: Results of the First 3 Years of Follow-up After Randomization. J Thorac Oncol 2015; 10: 890-896 https://www.ncbi.nlm.nih.gov/pubmed/25783198
- 32 Becker N, Motsch E, Trotter A. et al. Lung cancer mortality reduction by LDCT screening-Results from the randomized German LUSI trial. Int J Cancer 2020; 146: 1503-1513 https://pubmed.ncbi.nlm.nih.gov/31162856/
- 33 Spiro S. et al. Initial evaluattion of the patient with lung cancer: Symptoms, signs, laboratory tests, and paraneoplastic syndromes ACCP Evidenced-Based Clinical Practice Guidelines. Chest 2007; 132: 149S-160S https://www.ncbi.nlm.nih.gov/pubmed/17873166
- 34 Minna JD, Higgins GA, Glatstein E. Cancer of the lung. Cancer: Principles and Practice of Oncology 1985; 507-597 https://www.lungcancerjournal.info/article/0169-5002(89)90182-7/fulltext
- 35 Kreuter M. et al. Diagnostik des Bronchialkarzinoms. Pneumologe 2008; 5: 187-198
- 36 Bradley S, Abraham S, Callister M. et al. Sensitivity of chest X-ray for detecting lung cancer in people presenting with symptoms: a systematic review. Br J Gen Pract 2019; 69: e827-e835 https://pubmed.ncbi.nlm.nih.gov/31636130/
- 37 Kim J, Lee K, Kim K. et al. Comparison of digital tomosynthesis and chest radiography for the detection of pulmonary nodules: systematic review and meta-analysis. Br J Radiol 2016; 89: 20160421 https://pubmed.ncbi.nlm.nih.gov/27759428/
- 38 Neal R, Barham A, Bongard E. et al. Immediate chest X-ray for patients at risk of lung cancer presenting in primary care: randomised controlled feasibility trial. Br J Cancer 2017; 116: 293-302 https://pubmed.ncbi.nlm.nih.gov/28072761/
- 39 Li Y, Jin G, Su D. Comparison of Gadolinium-enhanced MRI and 18FDG PET/PET-CT for the diagnosis of brain metastases in lung cancer patients: A meta-analysis of 5 prospective studies. Oncotarget 2017; 8: 35743-35749 https://pubmed.ncbi.nlm.nih.gov/28415747/
- 40 Wu Q, Luo W, Zhao Y. et al. The utility of 18F-FDG PET/CT for the diagnosis of adrenal metastasis in lung cancer: a PRISMA-compliant meta-analysis. Nucl Med Commun 2017; 38: 1117-1124 https://pubmed.ncbi.nlm.nih.gov/28953208/
- 41 Martucci F, Pascale M, Valli M. et al. Impact of 18F-FDG PET/CT in Staging Patients With Small Cell Lung Cancer: A Systematic Review and Meta-Analysis. Front Med (Lausanne) 2019; 6: 336 https://pubmed.ncbi.nlm.nih.gov/32118000/
- 42 Mitchell M, Aggarwal C, Tsou A. et al. Imaging for the Pretreatment Staging of Small cell Lung Cancer: A Systematic Review. Acad Radiol 2016; 23: 1047-1056 https://pubmed.ncbi.nlm.nih.gov/27259379/
- 43 Kuijvenhoven J, Leoncini F, Crombag L. et al. Endobronchial Ultrasound for the Diagnosis of Centrally Located Lung Tumors: A Systematic Review and Meta-Analysis. Respiration 2020; 99: 441-450 https://pubmed.ncbi.nlm.nih.gov/31734666/
- 44 Sainz Zuñiga P, Vakil E, Molina S. et al. Sensitivity of Radial Endobronchial Ultrasound-Guided Bronchoscopy for Lung Cancer in Patients With Peripheral Pulmonary Lesions: An Updated Meta-analysis. Chest 2020; 157: 994-1011 https://pubmed.ncbi.nlm.nih.gov/31738928/
- 45 Ali M, Sethi J, Taneja A. et al. Computed Tomography Bronchus Sign and the Diagnostic Yield of Guided Bronchoscopy for Peripheral Pulmonary Lesions A Systematic Review and Meta-Analysis. Ann Am Thorac Soc 2018; 15: 978-987 https://pubmed.ncbi.nlm.nih.gov/29877715/
- 46 Mondoni M, Sotgiu G, Bonifazi M. et al. Transbronchial needle aspiration in peripheral pulmonary lesions: a systematic review and meta-analysis. Eur Respir J 2016; 48: 196-204 https://pubmed.ncbi.nlm.nih.gov/27174878/
- 47 Navani N, Nankivell M, Lawrence D. et al. Lung cancer diagnosis and staging with endobronchial ultrasound-guided transbronchial needle aspiration compared with conventional approaches: an open-label, pragmatic, randomised controlled trial. Lancet Respir Med 2015; 3: 282-289 https://pubmed.ncbi.nlm.nih.gov/25660225/
- 48 Korevaar D, Colella S, Spijker R. et al. Esophageal Endosonography for the Diagnosis of Intrapulmonary Tumors: A Systematic Review and Meta-Analysis. Respiration 2017; 93: 126-137 https://pubmed.ncbi.nlm.nih.gov/27926910/
- 49 Sehgal I, Dhooria S, Aggarwal A. et al. Endosonography Versus Mediastinoscopy in Mediastinal Staging of Lung Cancer: Systematic Review and Meta-Analysis. Ann Thorac Surg 2016; 102: 1747-1755 https://pubmed.ncbi.nlm.nih.gov/27637288/
- 50 Labarca G, Folch E, Jantz M. et al. Adequacy of Samples Obtained by Endobronchial Ultrasound with Transbronchial Needle Aspiration for Molecular Analysis in Patients with Non-Small Cell Lung Cancer Systematic Review and Meta-Analysis. Ann Am Thorac Soc 2018; 15: 1205-1216 https://pubmed.ncbi.nlm.nih.gov/30011388/
- 51 Layfield L, Pearson L, Walker B. et al. Diagnostic Accuracy of Fine-Needle Aspiration Cytology for Discrimination of Squamous Cell Carcinoma from Adenocarcinoma in Non-Small Cell Lung Cancer: A Systematic Review and Meta-Analysis. Acta Cytol 2018; 62: 318-326 https://pubmed.ncbi.nlm.nih.gov/30380531/
- 52 Gould M, Donington J, Lynch W. et al. Evaluation of individuals with pulmonary nodules: when is it lung cancer? Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143 (Suppl. 05) e93S-e120S https://pubmed.ncbi.nlm.nih.gov/23649456/
- 53 Bankier A, MacMahon H, Goo J. et al. Recommendations for Measuring Pulmonary Nodules at CT: A Statement from the Fleischner Society. Radiology 2017; 285: 584-600 https://pubmed.ncbi.nlm.nih.gov/28650738/
- 54 MacMahon H, Naidich D, Goo J. et al. Guidelines for Management of Incidental Pulmonary Nodules Detected on CT Images: From the Fleischner Society 2017. Radiology 2017; 284: 228-243 https://pubmed.ncbi.nlm.nih.gov/28240562/
- 55 Callister M, Baldwin D, Akram A. et al. British Thoracic Society guidelines for the investigation and management of pulmonary nodules. Thorax 2015; 70 (Suppl. 02) ii1-ii54 https://pubmed.ncbi.nlm.nih.gov/26082159/
- 56 Swensen S, Silverstein M, Ilstrup D. et al. The probability of malignancy in solitary pulmonary nodules Application to small radiologically indeterminate nodules. Arch Intern Med 1997; 157: 849-855 https://pubmed.ncbi.nlm.nih.gov/9129544/
- 57 Herder G, van Tinteren H, Golding R. et al. Clinical prediction model to characterize pulmonary nodules: validation and added value of 18F-fluorodeoxyglucose positron emission tomography. Chest 2005; 128: 2490-2496 https://pubmed.ncbi.nlm.nih.gov/16236914/
- 58 McWilliams A, Tammemagi M, Mayo J. et al. Probability of cancer in pulmonary nodules detected on first screening CT. N Engl J Med 2013; 369: 910-919 https://pubmed.ncbi.nlm.nih.gov/24004118/
- 59 Tan BB, Flaherty KR, Kazerooni EA. et al. The solitary pulmonary nodule. Chest 2003; 123 (Suppl. 01) 89S-96S https://www.ncbi.nlm.nih.gov/pubmed/12527568
- 60 Ost D, Fein AM, Feinsilver SH. Clinical practice The solitary pulmonary nodule. N Engl J Med 2003; 348: 2535-2542 https://www.ncbi.nlm.nih.gov/pubmed/12815140
- 61 Gould MK, Fletcher J, Iannettoni MD. et al. Evaluation of patients with pulmonary nodules: when is it lung cancer?: ACCP evidence-based clinical practice guidelines (2nd edition). Chest 2007; 132 (Suppl. 03) 108S-130S https://www.ncbi.nlm.nih.gov/pubmed/17873164
- 62 Aberle D, DeMello S, Berg C. et al. Results of the two incidence screenings in the National Lung Screening Trial. N Engl J Med 2013; 369: 920-931 https://pubmed.ncbi.nlm.nih.gov/24004119/
- 63 Revel M, Bissery A, Bienvenu M. et al. Are two-dimensional CT measurements of small noncalcified pulmonary nodules reliable?. Radiology 2004; 231: 453-458 https://pubmed.ncbi.nlm.nih.gov/15128990/
- 64 Horeweg N, Scholten ET, de Jong PA. et al. Detection of lung cancer through low-dose CT screening (NELSON): a prespecified analysis of screening test performance and interval cancers. Lancet Oncol 2014; 15: 1342-1350 https://www.ncbi.nlm.nih.gov/pubmed/25282284
- 65 Matsuguma H, Mori K, Nakahara R. et al. Characteristics of subsolid pulmonary nodules showing growth during follow-up with CT scanning. Chest 2013; 143: 436-443 https://pubmed.ncbi.nlm.nih.gov/22814723/
- 66 Ichinose J, Kohno T, Fujimori S. et al. Invasiveness and malignant potential of pulmonary lesions presenting as pure ground-glass opacities. Ann Thorac Cardiovasc Surg 2014; 20: 347-352 https://pubmed.ncbi.nlm.nih.gov/24088912/
- 67 Gould M, Maclean C, Kuschner W. et al. Accuracy of positron emission tomography for diagnosis of pulmonary nodules and mass lesions: a meta-analysis. JAMA 2001; 285: 914-924 https://pubmed.ncbi.nlm.nih.gov/11180735/
- 68 Deppen S, Blume J, Kensinger C. et al. Accuracy of FDG-PET to diagnose lung cancer in areas with infectious lung disease: a meta-analysis. JAMA 2014; 312: 1227-1236 https://pubmed.ncbi.nlm.nih.gov/25247519/
- 69 Cardillo G, Regal M, Sera F. et al. Videothoracoscopic management of the solitary pulmonary nodule: a single-institution study on 429 cases. Ann Thorac Surg 2003; 75: 1607-1611 discussion 1611-1612 https://pubmed.ncbi.nlm.nih.gov/12735587/
- 70 Petersen R, Hansen H, Dirksen A. et al. Lung cancer screening and video-assisted thoracic surgery. J Thorac Oncol 2012; 7: 1026-1031 https://pubmed.ncbi.nlm.nih.gov/22588154/
- 71 Field J, Smith R, Aberle D. et al. International Association for the Study of Lung Cancer Computed Tomography Screening Workshop 2011 report. J Thorac Oncol 2012; 7: 10-19 https://pubmed.ncbi.nlm.nih.gov/22173661/
- 72 Berman A, Jabbour S, Vachani A. et al. Empiric Radiotherapy for Lung Cancer Collaborative Group multi-institutional evidence-based guidelines for the use of empiric stereotactic body radiation therapy for non-small cell lung cancer without pathologic confirmation. Transl Lung Cancer Res 2019; 8: 5-14 https://pubmed.ncbi.nlm.nih.gov/30788230/
- 73 IJsseldijk M, Shoni M, Siegert C. et al. Survival After Stereotactic Body Radiation Therapy for Clinically Diagnosed or Biopsy-Proven Early-Stage NSCLC: A Systematic Review and Meta-Analysis. J Thorac Oncol 2019; 14: 583-595 https://pubmed.ncbi.nlm.nih.gov/30721798/
- 74 Travis W, Asamura H, Bankier A. et al. The IASLC Lung Cancer Staging Project: Proposals for Coding T Categories for Subsolid Nodules and Assessment of Tumor Size in Part-Solid Tumors in the Forthcoming Eighth Edition of the TNM Classification of Lung Cancer. J Thorac Oncol 2016; 11: 1204-1223 https://pubmed.ncbi.nlm.nih.gov/27107787/
- 75 Rami-Porta R, Bolejack V, Crowley J. et al. The IASLC Lung Cancer Staging Project: Proposals for the Revisions of the T Descriptors in the Forthcoming Eighth Edition of the TNM Classification for Lung Cancer. J Thorac Oncol 2015; 10: 990-1003 https://pubmed.ncbi.nlm.nih.gov/26134221/
- 76 Nicholson AG. The International Association for the Study of Lung Cancer Lung Cancer Staging Project: Proposals for the Revision of the Clinical and Pathologic Staging of Small Cell Lung Cancer in the Forthcoming Eighth Edition of the TNM Classification for Lung Cancer. Journal of Thoracic Oncology 2016; 11: 300-311 https://www.ncbi.nlm.nih.gov/pubmed/26723244
- 77 Robinson LA, Wagner H, Ruckdeschel JC. Treatment of stage IIIA non-small cell lung cancer. Chest 2003; 123: 202S-220S https://www.ncbi.nlm.nih.gov/pubmed/12527580
- 78 Robinson LA, Ruckdeschel JC, Wagner H. et al. Treatment of non-small cell lung cancer-stage IIIA: ACCP evidence-based clinical practice guidelines (2nd edition). Chest 2007; 132: 243S-265S https://www.ncbi.nlm.nih.gov/pubmed/17873172
- 79 Rusch VW, Asamura H, Watanabe H. et al. The IASLC lung cancer staging project: a proposal for a new international lymph node map in the forthcoming seventh edition of the TNM classification for lung cancer. J Thorac Oncol 2009; 4: 568-577 https://www.ncbi.nlm.nih.gov/pubmed/19357537
- 80 Eberhardt WE, Mitchell A, Crowley J. et al. The IASLC Lung Cancer Staging Project: Proposals for the Revision of the M Descriptors in the Forthcoming Eighth Edition of the TNM Classification of Lung Cancer. J Thorac Oncol 2015; 10: 1515-1522 https://www.ncbi.nlm.nih.gov/pubmed/26536193
- 81 Wittekind C. TNM: Klassifikation maligner Tumoren. 2017
- 82 Travis WD, Brambilla E, Nicholson AG. et al. The 2015 World Health Organization Classification of Lung Tumors: Impact of Genetic, Clinical and Radiologic Advances Since the 2004 Classification. J Thorac Oncol 2015; 10: 1243-1260 https://www.ncbi.nlm.nih.gov/pubmed/26291008
- 83 von Laffert M, Schirmacher P, Warth A. et al. Stellungnahme der DGP und der AG Thorakale Onkologie der AG Onkologie/Deutsche Krebsgesellschaft e V zur ALK-Testung beim NSCLC. Der Pathologe 2016; 37: 187-192 https://doi.org/10.1007/s00292-016-0152-1
- 84 Eagle KA, Guyton RA, Davidoff R. et al. ACC/AHA guidelines for coronary artery bypass graft surgery: executive summary and recommendations : A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to revise the 1991 guidelines for coronary artery bypass graft surgery). Circulation 1999; 100: 1464-1480 https://www.ncbi.nlm.nih.gov/pubmed/10500052
- 85 British Thoracic Society; Society of Cardiothoracic Surgeons of Great Britain and Ireland Working Party. BTS guidelines: guidelines on the selection of patients with lung cancer for surgery. Thorax 2001; 56: 89-108 https://www.ncbi.nlm.nih.gov/pubmed/11209097
- 86 Kappauf H. Kommunikation in der Onkologie. Onkologe 2004; 10: 1251-1260
- 87 Kuhlmann E. Spannungsfeld zwischen Informed Consent und konfliktvermeidender Fehlinformation: Patientenaufklärung unter ökonomischen Zwängen Ergebnisse einer empirischen Studie. Ethik Med 1999; 11: 146-161 https://link.springer.com/article/10.1007/s004810050070
- 88 Bundesministerium für Gesundheit. Patientenrechtegesetz. 2013
- 89 Schröder C, Schmutzer G, Brähler E. Repräsentativbefragung der deutschen Bevölkerung zu Aufklärungswunsch und Patientenverfügung bei unheilbarer Krankheit. Psychother Psychosom Med Psychol 2002; 52: 236-243
- 90 Baile WF, Kudelka AP, Beale EA. et al. Communication skills training in oncology Description and preliminary outcomes of workshops on breaking bad news and managing patient reactions to illness. Cancer 1999; 86: 887-897 https://www.ncbi.nlm.nih.gov/pubmed/10463990
- 91 Keller M, Werner A. Aufklärung und Begleitung von Tumorpatienten – Trainingsprogramme für Ärzte. Onkologe 2006; 12: 55-61
- 92 Beauchamp TL, Childress JF. Principles of Biomedical Ethics. 1994 4th.
- 93 Informed Consent im klinischen Alltag – eine pragmatische Interpretation. Ethik Med 2002; 14: 151-159 https://link.springer.com/article/10.1007/s00481-002-0165-6
- 94 Ernst J, Krauá O, Schwarz R. Die Einbeziehung von Tumorpatienten in medizinische Entscheidungsprozesse. Onkologe 2006; 12: 48-54
- 95 Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft DK, AWMF): Palliativmedizin für Patienten mit einer nicht heilbaren Krebserkrankung, Langversion 11. AWMF-Registernummer: 128/001OL. 2015 http://leitlinienprogrammonkologie.de/Palliativmedizin.80.0.html (Zugriff am: 29.10.2015)
- 96 Bruera E, Willey JS, Palmer JL. et al. Treatment decisions for breast carcinoma: patient preferences and physician perceptions. Cancer 2002; 94: 2076-2080 https://www.ncbi.nlm.nih.gov/pubmed/11932912
- 97 Butow P, Harrison JD, Choy ET. et al. Health professional and consumer views on involving breast cancer patients in the multidisciplinary discussion of their disease and treatment plan. Cancer 2007; 110: 1937-1944 https://www.ncbi.nlm.nih.gov/pubmed/17823912
- 98 Elkin EB, Kim SH, Casper ES. et al. Desire for information and involvement in treatment decisions: elderly cancer patients' preferences and their physicians' perceptions. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 2007; 25: 5275-5280 https://www.ncbi.nlm.nih.gov/pubmed/18024875
- 99 Ford S, Schofield T, Hope T. Observing decision-making in the general practice consultation: who makes which decisions?. Health Expect 2006; 9: 130-137 https://www.ncbi.nlm.nih.gov/pubmed/16677192
- 100 Politi MC, Han PK, Col NF. Communicating the uncertainty of harms and benefits of medical interventions. Med Decis Making 2007; 27: 681-695 https://www.ncbi.nlm.nih.gov/pubmed/17873256
- 101 National Institute for Clinical Excellence (NICE). The Diagnosis and Treatment of Lung Cancer. NICE guideline: https://www.nice.org.uk/guidance/ng122
- 102 Temel JS, Greer JA, Muzikansky A. et al. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med 2010; 363: 733-742 https://www.ncbi.nlm.nih.gov/pubmed/20818875
- 103 Bakitas M, Lyons KD, Hegel MT. et al. Effects of a palliative care intervention on clinical outcomes in patients with advanced cancer: the Project ENABLE II randomized controlled trial. JAMA 2009; 302: 741-749 https://www.ncbi.nlm.nih.gov/pubmed/19690306
- 104 Greer JA, Pirl WF, Jackson VA. et al. Effect of early palliative care on chemotherapy use and end-of-life care in patients with metastatic non-small-cell lung cancer. J Clin Oncol 2012; 30: 394-400 https://www.ncbi.nlm.nih.gov/pubmed/22203758
- 105 Badr H, Smith CB, Goldstein NE. et al. Dyadic psychosocial intervention for advanced lung cancer patients and their family caregivers: Results of a randomized pilot trial. Cancer 2015; 121: 150-158 https://www.ncbi.nlm.nih.gov/pubmed/25209975
- 106 Zimmermann C, Swami N, Krzyzanowska M. et al. Early palliative care for patients with advanced cancer: a cluster-randomised controlled trial. Lancet 2014; 383: 1721-1730 https://www.ncbi.nlm.nih.gov/pubmed/24559581
- 107 Bakitas MA, Tosteson TD, Li Z. et al. Early Versus Delayed Initiation of Concurrent Palliative Oncology Care: Patient Outcomes in the ENABLE III Randomized Controlled Trial. J Clin Oncol 2015; 33: 1438-1445 https://www.ncbi.nlm.nih.gov/pubmed/25800768
- 108 Ball D, Mai G, Vinod S. et al. Stereotactic ablative radiotherapy versus standard radiotherapy in stage 1 non-small-cell lung cancer (TROG 0902 CHISEL): a phase 3, open-label, randomised controlled trial. Lancet Oncol 2019; 20: 494-503 https://pubmed.ncbi.nlm.nih.gov/30770291/
- 109 Fernando H, Landreneau R, Mandrekar S. et al. Impact of brachytherapy on local recurrence rates after sublobar resection: results from ACOSOG Z4032 (Alliance), a phase III randomized trial for high-risk operable non-small-cell lung cancer. J Clin Oncol 2014; 32: 2456-2462 https://pubmed.ncbi.nlm.nih.gov/24982457/
- 110 Verstegen N, Lagerwaard F, Haasbeek C. et al. Outcomes of stereotactic ablative radiotherapy following a clinical diagnosis of stage I NSCLC: comparison with a contemporaneous cohort with pathologically proven disease. Radiother Oncol 2011; 101: 250-254 https://pubmed.ncbi.nlm.nih.gov/22056535/
- 111 Taremi M, Hope A, Dahele M. et al. Stereotactic body radiotherapy for medically inoperable lung cancer: prospective, single-center study of 108 consecutive patients. Int J Radiat Oncol Biol Phys 2012; 82: 967-973 https://pubmed.ncbi.nlm.nih.gov/21377293/
- 112 Creach K, El Naqa I, Bradley J. et al. Dosimetric predictors of chest wall pain after lung stereotactic body radiotherapy. Radiother Oncol 2012; 104: 23-27 https://pubmed.ncbi.nlm.nih.gov/22385795/
- 113 Grills I, Hope A, Guckenberger M. et al. A collaborative analysis of stereotactic lung radiotherapy outcomes for early-stage non-small-cell lung cancer using daily online cone-beam computed tomography image-guided radiotherapy. J Thorac Oncol 2012; 7: 1382-1393 https://pubmed.ncbi.nlm.nih.gov/22843086/
- 114 Senthi S, Haasbeek C, Slotman B. et al. Outcomes of stereotactic ablative radiotherapy for central lung tumours: a systematic review. Radiother Oncol 2013; 106: 276-282 https://pubmed.ncbi.nlm.nih.gov/23462705/
- 115 Bezjak A, Paulus R, Gaspar L. et al. Safety and Efficacy of a Five-Fraction Stereotactic Body Radiotherapy Schedule for Centrally Located Non-Small-Cell Lung Cancer: NRG Oncology/RTOG 0813 Trial. J Clin Oncol 2019; 37: 1316-1325 https://pubmed.ncbi.nlm.nih.gov/30943123/
- 116 Haasbeek C, Lagerwaard F, Slotman B. et al. Outcomes of stereotactic ablative radiotherapy for centrally located early-stage lung cancer. J Thorac Oncol 2011; 6: 2036-2043 https://pubmed.ncbi.nlm.nih.gov/21892102/
- 117 Timmerman R, McGarry R, Yiannoutsos C. et al. Excessive toxicity when treating central tumors in a phase II study of stereotactic body radiation therapy for medically inoperable early-stage lung cancer. J Clin Oncol 2006; 24: 4833-4839 https://pubmed.ncbi.nlm.nih.gov/17050868/
- 118 Zhang J, Yang F, Li B. et al. Which is the optimal biologically effective dose of stereotactic body radiotherapy for Stage I non-small-cell lung cancer? A meta-analysis. Int J Radiat Oncol Biol Phys 2011; 81: e305-e316 https://pubmed.ncbi.nlm.nih.gov/21658853/
- 119 Stahl J, Ross R, Harder E. et al. The Effect of Biologically Effective Dose and Radiation Treatment Schedule on Overall Survival in Stage I Non-Small Cell Lung Cancer Patients Treated With Stereotactic Body Radiation Therapy. Int J Radiat Oncol Biol Phys 2016; 96: 1011-1020 https://pubmed.ncbi.nlm.nih.gov/27869080/
- 120 Raz D, Zell J, Ou S. et al. Natural history of stage I non-small cell lung cancer: implications for early detection. Chest 2007; 132: 193-199 https://pubmed.ncbi.nlm.nih.gov/17505036/
- 121 Cao C, Wang D, Chung C. et al. A systematic review and meta-analysis of stereotactic body radiation therapy versus surgery for patients with non-small cell lung cancer. J Thorac Cardiovasc Surg 2019; 157: 362-373.e8 https://pubmed.ncbi.nlm.nih.gov/30482524/
- 122 De Ruysscher D, Faivre-Finn C, Nestle U. et al. European Organisation for Research and Treatment of Cancer recommendations for planning and delivery of high-dose, high-precision radiotherapy for lung cancer. J Clin Oncol 2010; 28: 5301-5310 https://pubmed.ncbi.nlm.nih.gov/21079134/
- 123 Fernandez F, Crabtree T, Liu J. et al. Sublobar resection versus definitive radiation in patients with stage IA non-small cell lung cancer. Ann Thorac Surg 2012; 94: 354-360 discussion 360-361 https://pubmed.ncbi.nlm.nih.gov/22429673/
- 124 Ezer N, Veluswamy R, Mhango G. et al. Outcomes after Stereotactic Body Radiotherapy versus Limited Resection in Older Patients with Early-Stage Lung Cancer. J Thorac Oncol 2015; 10: 1201-1206 https://pubmed.ncbi.nlm.nih.gov/26200275/
- 125 Mokhles S, Verstegen N, Maat A. et al. Comparison of clinical outcome of stage I non-small cell lung cancer treated surgically or with stereotactic radiotherapy: results from propensity score analysis. Lung Cancer 2015; 87: 283-289 https://pubmed.ncbi.nlm.nih.gov/25622781/
- 126 Yerokun B, Yang C, Gulack B. et al. A national analysis of wedge resection versus stereotactic body radiation therapy for stage IA non-small cell lung cancer. J Thorac Cardiovasc Surg 2017; 154: 675-686.e4 https://pubmed.ncbi.nlm.nih.gov/28461054/
- 127 Varlotto J, Fakiris A, Flickinger J. et al. Matched-pair and propensity score comparisons of outcomes of patients with clinical stage I non-small cell lung cancer treated with resection or stereotactic radiosurgery. Cancer 2013; 119: 2683-2691 https://pubmed.ncbi.nlm.nih.gov/23605504/
- 128 Palma D, Lagerwaard F, Rodrigues G. et al. Curative treatment of Stage I non-small-cell lung cancer in patients with severe COPD: stereotactic radiotherapy outcomes and systematic review. Int J Radiat Oncol Biol Phys 2012; 82: 1149-1156 https://pubmed.ncbi.nlm.nih.gov/21640513/
- 129 Guckenberger M, Andratschke N, Alheit H. et al. Definition of stereotactic body radiotherapy: principles and practice for the treatment of stage I non-small cell lung cancer. Strahlenther Onkol 2014; 190: 26-33 https://pubmed.ncbi.nlm.nih.gov/24052011/
- 130 Benedict S, Yenice K, Followill D. et al. Stereotactic body radiation therapy: the report of AAPM Task Group 101. Med Phys 2010; 37: 4078-4101 https://pubmed.ncbi.nlm.nih.gov/20879569/
- 131 Ferguson MK, Lehman AG. Sleeve lobectomy or pneumonectomy: optimal management strategy using decision analysis techniques. Ann Thorac Surg 2003; 76: 1782-1788 https://www.ncbi.nlm.nih.gov/pubmed/14667584
- 132 Detterbeck FC. General aspects of surgical treatment. In: Diagnosis and treatment of lung cancer: an evidence-based guide for the practicing clinician (Detterbeck FC, Rivera MP, Socinski MA, Roseman JG, eds.). 2001: 133-147
- 133 Harpole DH, DeCamp MM, Daley J. et al. Prognostic models of thirty-day mortality and morbidity after major pulmonary resection. J Thorac Cardiovasc Surg 1999; 117: 969-979 https://www.ncbi.nlm.nih.gov/pubmed/10220692
- 134 Ginsberg RJ, Rubinstein LV. Randomized trial of lobectomy versus limited resection for T1 N0 non-small cell lung cancer Lung Cancer Study Group. Ann Thorac Surg 1995; 60: 615-622 https://www.ncbi.nlm.nih.gov/pubmed/7677489
- 135 Harada H, Okada M, Sakamoto T. et al. Functional advantage after radical segmentectomy versus lobectomy for lung cancer. Ann Thorac Surg 2005; 80: 2041-2045 https://www.ncbi.nlm.nih.gov/pubmed/16305841
- 136 Keenan RJ, Landreneau RJ, Maley RH. et al. Segmental resection spares pulmonary function in patients with stage I lung cancer. Ann Thorac Surg 2004; 78: 228-233 https://www.ncbi.nlm.nih.gov/pubmed/15223434
- 137 Okada M, Yoshikawa K, Hatta T. et al. Is segmentectomy with lymph node assessment an alternative to lobectomy for non-small cell lung cancer of 2 cm or smaller?. Ann Thorac Surg 2001; 71: 956-960 https://www.ncbi.nlm.nih.gov/pubmed/11269480
- 138 Date H, Andou A, Shimizu N. The value of limited resection for “clinical” stage I peripheral non-small cell lung cancer in poor-risk patients: comparison of limited resection and lobectomy by a computer-assisted matched study. Tumori 1994; 80: 422-426 https://www.ncbi.nlm.nih.gov/pubmed/7900230
- 139 Allen MS, Darling GE, Pechet TT. et al. Morbidity and mortality of major pulmonary resections in patients with early-stage lung cancer: initial results of the randomized, prospective ACOSOG Z0030 trial. Ann Thorac Surg 2006; 81: 1013-1019 https://www.ncbi.nlm.nih.gov/pubmed/16488712
- 140 Powell J, Dexter E, Scalzetti E. et al. Treatment advances for medically inoperable non-small-cell lung cancer: emphasis on prospective trials. Lancet Oncol 2009; 10: 885-894 https://pubmed.ncbi.nlm.nih.gov/19717090/
- 141 Onishi H, Shirato H, Nagata Y. et al. Hypofractionated Stereotactic Radiotherapy (HypoFXSRT) for Stage I Non-small Cell Lung Cancer: Updated Results of 257 Patients in a Japanese Multi-institutional Study. J Thorac Oncol 2007; 2: S94-S100 https://www.ncbi.nlm.nih.gov/pubmed/17603311
- 142 Shirvani S, Jiang J, Chang J. et al. Comparative effectiveness of 5 treatment strategies for early-stage non-small cell lung cancer in the elderly. Int J Radiat Oncol Biol Phys 2012; 84: 1060-1070 https://pubmed.ncbi.nlm.nih.gov/22975611/
- 143 Paul S, Lee P, Mao J. et al. Long term survival with stereotactic ablative radiotherapy (SABR) versus thoracoscopic sublobar lung resection in elderly people: national population based study with propensity matched comparative analysis. BMJ 2016; 354: i3570 https://pubmed.ncbi.nlm.nih.gov/27400862/
- 144 Grills I, Mangona V, Welsh R. et al. Outcomes after stereotactic lung radiotherapy or wedge resection for stage I non-small-cell lung cancer. J Clin Oncol 2010; 28: 928-935 https://pubmed.ncbi.nlm.nih.gov/20065181/
- 145 Cao C, Wang D, Chung C. et al. A systematic review and meta-analysis of stereotactic body radiation therapy versus surgery for patients with non-small cell lung cancer. J Thorac Cardiovasc Surg 2019; 157: 362-373.e8 https://pubmed.ncbi.nlm.nih.gov/30482524/
- 146 Li H, Shen Y, Wu Y. et al. Stereotactic Body Radiotherapy Versus Surgery for Early-Stage Non-Small-Cell Lung Cancer. J Surg Res 2019; 243: 346-353 https://pubmed.ncbi.nlm.nih.gov/31277011/
- 147 Wen S, Han L, Lv H. et al. A Propensity-Matched Analysis of Outcomes of Patients with Clinical Stage I Non-Small Cell Lung Cancer Treated surgically or with stereotactic radiotherapy: A Meta-Analysis. J Invest Surg 2019; 32: 27-34 https://pubmed.ncbi.nlm.nih.gov/28985095/
- 148 Mountain CF. Revisions in the International System for Staging Lung Cancer. Chest 1997; 111: 1710-1717 https://www.ncbi.nlm.nih.gov/pubmed/9187198
- 149 Okada M, Nishio W, Sakamoto T. et al. Evolution of surgical outcomes for nonsmall cell lung cancer: time trends in 1465 consecutive patients undergoing complete resection. Ann Thorac Surg 2004; 77: 1926-1930 https://www.ncbi.nlm.nih.gov/pubmed/15172237
- 150 Licker M, Spiliopoulos A, Frey JG. et al. Management and outcome of patients undergoing thoracic surgery in a regional chest medical centre. Eur J Anaesthesiol 2001; 18: 540-547 https://www.ncbi.nlm.nih.gov/pubmed/11473561
- 151 Bernard A, Ferrand L, Hagry O. et al. Identification of prognostic factors determining risk groups for lung resection. Ann Thorac Surg 2000; 70: 1161-1167 https://www.ncbi.nlm.nih.gov/pubmed/11081862
- 152 Battafarano RJ, Piccirillo JF, Meyers BF. et al. Impact of comorbidity on survival after surgical resection in patients with stage I non-small cell lung cancer. J Thorac Cardiovasc Surg 2002; 123: 280-287 https://www.ncbi.nlm.nih.gov/pubmed/11828287
- 153 Van Meerbeeck JP, Damhuis RA, Vos de Wael ML. High postoperative risk after pneumonectomy in elderly patients with right-sided lung cancer. Eur Respir J 2002; 19: 141-145 https://www.ncbi.nlm.nih.gov/pubmed/11852891
- 154 Sok M, Dragas AZ, Erzen J. et al. Sources of pathogens causing pleuropulmonary infections after lung cancer resection. Eur J Cardiothorac Surg 2002; 22: 23-27 https://www.ncbi.nlm.nih.gov/pubmed/12103368
- 155 Wahi R, McMurtrey MJ, DeCaro LF. et al. Determinants of perioperative morbidity and mortality after pneumonectomy. Ann Thorac Surg 1989; 48: 33-37 https://www.ncbi.nlm.nih.gov/pubmed/2764597
- 156 Bao F, Ye P, Yang Y. et al. Segmentectomy or lobectomy for early stage lung cancer: a meta-analysis. Eur J Cardiothorac Surg 2014; 46: 1-7 https://pubmed.ncbi.nlm.nih.gov/24321996/
- 157 Licker MJ, Widikker I, Robert J. et al. Operative mortality and respiratory complications after lung resection for cancer: impact of chronic obstructive pulmonary disease and time trends. Ann Thorac Surg 2006; 81: 1830-1837 https://www.ncbi.nlm.nih.gov/pubmed/16631680
- 158 Weinmann M, Jeremic B, Toomes H. et al. Treatment of lung cancer in the elderly Part I: non-small cell lung cancer. Lung Cancer 2003; 39: 233-253 https://www.ncbi.nlm.nih.gov/pubmed/12609562
- 159 Ng C, MacDonald J, Gilbert S. et al. Optimal Approach to Lobectomy for Non-Small Cell Lung Cancer: Systemic Review and Meta-Analysis. Innovations (Phila) 2019; 14: 90-116 https://pubmed.ncbi.nlm.nih.gov/31039680/
- 160 Wang Z, Pang L, Tang J. et al. Video-assisted thoracoscopic surgery versus muscle-sparing thoracotomy for non-small cell lung cancer: a systematic review and meta-analysis. BMC Surg 2019; 19: 144 https://pubmed.ncbi.nlm.nih.gov/31615490/
- 161 Bendixen M, Jørgensen O, Kronborg C. et al. Postoperative pain and quality of life after lobectomy via video-assisted thoracoscopic surgery or anterolateral thoracotomy for early stage lung cancer: a randomised controlled trial. Lancet Oncol 2016; 17: 836-844 https://pubmed.ncbi.nlm.nih.gov/27160473/
- 162 Long H, Tan Q, Luo Q. et al. Thoracoscopic Surgery Versus Thoracotomy for Lung Cancer: Short-Term Outcomes of a Randomized Trial. Ann Thorac Surg 2018; 105: 386-392 https://pubmed.ncbi.nlm.nih.gov/29198623/
- 163 Palade E, Passlick B, Osei-Agyemang T. et al. Video-assisted vs open mediastinal lymphadenectomy for Stage I non-small-cell lung cancer: results of a prospective randomized trial. Eur J Cardiothorac Surg 2013; 44: 244-249 discussion 249 https://pubmed.ncbi.nlm.nih.gov/23295451/
- 164 Wang Y. Video-assisted thoracoscopic surgery for non-small-cell lung cancer is beneficial to elderly patients. Int J Clin Exp Med 2015; 8: 13604-3609 https://pubmed.ncbi.nlm.nih.gov/26550301/
- 165 Yang H, Liu X, Meng X. et al. Efficacy of video-assisted thoracoscopic surgery for radical resection of non-small cell lung cancer in elderly patients. Int J Clin Exp Med 2019; 12: 2675-2682 http://www.ijcem.com/files/ijcem0087398.pdf
- 166 Wu Y, Huang ZF, Wang SY. et al. A randomized trial of systematic nodal dissection in resectable non-small cell lung cancer. Lung Cancer 2002; 36: 1-6 https://www.ncbi.nlm.nih.gov/pubmed/11891025
- 167 Sugi K, Nawata K, Fujita N. et al. Systematic lymph node dissection for clinically diagnosed peripheral non-small-cell lung cancer less than 2 cm in diameter. World J Surg 1998; 22: 290-294 https://www.ncbi.nlm.nih.gov/pubmed/9494422
- 168 Izbicki JR, Thetter O, Habekost M. et al. Radical systematic mediastinal lymphadenectomy in non-small cell lung cancer: a randomized controlled trial. Br J Surg 1994; 81: 229-235 https://www.ncbi.nlm.nih.gov/pubmed/8156344
- 169 Izbicki JR, Passlick B, Karg O. et al. Impact of radical systematic mediastinal lymphadenectomy on tumor staging in lung cancer. Ann Thorac Surg 1995; 59: 209-214
- 170 Keller SM, Adak S, Wagner H. et al. A randomized trial of postoperative adjuvant therapy in patients with completely resected stage II or IIIA non-small-cell lung cancer Eastern Cooperative Oncology Group. N Engl J Med 2000; 343: 1217-1222 https://www.ncbi.nlm.nih.gov/pubmed/11071672
- 171 Perng RP, Wu MF, Lin SY. et al. A phase I feasibility and pharmacokinetic study of intrapleural paclitaxel in patients with malignant pleural effusions. Anticancer Drugs 1997; 8: 565-573 https://www.ncbi.nlm.nih.gov/pubmed/9300570
- 172 Wright G, Manser RL, Jart D. et al. Surgery for early stage non-small cell lung cancer (Review). The Cochrane Library 2006 https://www.ncbi.nlm.nih.gov/pubmed/15674959
- 173 Scott WJ, Howington J, Movsas B. Treatment of stage II non-small cell lung cancer. Chest 2003; 123: 188S-201S https://www.ncbi.nlm.nih.gov/pubmed/12527579
- 174 Magdeleinat P, Alifano M, Benbrahem C. et al. Surgical treatment of lung cancer invading the chest wall: results and prognostic factors. Ann Thorac Surg 2001; 71: 1094-1099 https://www.ncbi.nlm.nih.gov/pubmed/11308142
- 175 McCaughan BC, Martini N, Bains MS. et al. Chest wall invasion in carcinoma of the lung Therapeutic and prognostic implications. J Thorac Cardiovasc Surg 1985; 89: 836-841 https://www.ncbi.nlm.nih.gov/pubmed/2987619
- 176 Albertucci M, DeMeester TR, Rothberg M. et al. Surgery and the management of peripheral lung tumors adherent to the parietal pleura. J Thorac Cardiovasc Surg 1992; 103: 8-12 https://www.ncbi.nlm.nih.gov/pubmed/1309467
- 177 Trastek VF, Pairolero PC, Piehler JM. et al. En bloc (non-chest wall) resection for bronchogenic carcinoma with parietal fixation Factors affecting survival. J Thorac Cardiovasc Surg 1984; 87: 352-358 https://www.ncbi.nlm.nih.gov/pubmed/6700242
- 178 Downey RJ, Martini N, Rusch VW. et al. Extent of chest wall invasion and survival in patients with lung cancer. Ann Thorac Surg 1999; 68: 188-193 https://www.ncbi.nlm.nih.gov/pubmed/10421139
- 179 Gould PM, Bonner JA, Sawyer TE. et al. Patterns of failure and overall survival in patients with completely resected T3 N0 M0 non-small cell lung cancer. Int J Radiat Oncol Biol Phys 1999; 45: 91-95 https://www.ncbi.nlm.nih.gov/pubmed/10477011
- 180 Depierre A, Milleron B, Moro-Sibilot D. et al. Preoperative chemotherapy followed by surgery compared with primary surgery in resectable stage I (except T1N0), II, and IIIa non-small-cell lung cancer (Comment see De-Pas, T et al and Mok, T et al, J Clin Oncol Vol 20, 2603-4 and 2604-5). J Clin Oncol 2002; 20: 247-253 https://www.ncbi.nlm.nih.gov/pubmed/11773176
- 181 Nicolson M, Gilligan D, Smith I. et al. Pre-operative chemotherapy in patients with resectable non-small cell lung cancer (NSCLC): First results of the MRC LU22/NVALT/EORTC 08012 multi-centre randomised trial. J Clin Oncol 2007; 25: 7518 https://www.ncbi.nlm.nih.gov/pubmed/17544497
- 182 Scagliotti GV, Pastorino U, Vansteenkiste JF. et al. Randomized phase III study of surgery alone or surgery plus preoperative cisplatin and gemcitabine in stages IB to IIIA non-small-cell lung cancer. J Clin Oncol 2012; 30: 172-178 https://www.ncbi.nlm.nih.gov/pubmed/22124104
- 183 Felip E, Rosell R, Maestre JA. et al. Preoperative chemotherapy plus surgery versus surgery plus adjuvant chemotherapy versus surgery alone in early-stage non-small-cell lung cancer. J Clin Oncol 2010; 28: 3138-3145 https://www.ncbi.nlm.nih.gov/pubmed/20516435
- 184 Preoperative chemotherapy for non-small-cell lung cancer: a systematic review and meta-analysis of individual participant data. Lancet 2014; 383: 1561-1571 https://www.ncbi.nlm.nih.gov/pubmed/24576776
- 185 Forde P, Spicer J, Lu S. et al. Neoadjuvant Nivolumab plus Chemotherapy in Resectable Lung Cancer. N Engl J Med 2022; 386: 1973-1985 https://pubmed.ncbi.nlm.nih.gov/35403841/
- 186 Pisters K, Vallieres E, Bunn PA. et al. S9900: Surgery alone or surgery plus induction (ind) paclitaxel/carboplatin (PC) chemotherapy in early stage non-small cell lung cancer (NSCLC): Follow-up on a phase III trial. J Clin Oncol 2007; 25: 7520
- 187 West H, McCleod M, Hussein M. et al. Atezolizumab in combination with carboplatin plus nab-paclitaxel chemotherapy compared with chemotherapy alone as first-line treatment for metastatic non-squamous non-small-cell lung cancer (IMpower130): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol 2019; 20: 924-937 https://pubmed.ncbi.nlm.nih.gov/31122901/
- 188 Burdett S, Pignon J, Tierney J. et al. Adjuvant chemotherapy for resected early-stage non-small cell lung cancer. Cochrane Database Syst Rev 2015; CD011430 https://pubmed.ncbi.nlm.nih.gov/25730344/
- 189 Arriagada R, Auperin A, Burdett S. et al. Adjuvant chemotherapy, with or without postoperative radiotherapy, in operable non-small-cell lung cancer: two meta-analyses of individual patient data. Lancet 2010; 375: 1267-1277 https://pubmed.ncbi.nlm.nih.gov/20338627/
- 190 Sedrakyan A, Van Der MJ, O’Byrne K. et al. Postoperative chemotherapy for non-small cell lung cancer: A systematic review and meta-analysis. J Thorac Cardiovasc Surg 2004; 128: 414-419 https://www.ncbi.nlm.nih.gov/pubmed/15354101
- 191 Pignon JP, Stewart LA. Randomized trials of radiotherapy alone versus combined chemotherapy and radiotherapy in stages IIIa and IIIb nonsmall cell lung cancer: a meta-analysis (Comment to Marino, P, Cancer, Vol 76, p 593–601). Cancer 1996; 77: 2413-2414 https://www.ncbi.nlm.nih.gov/pubmed/8625152
- 192 Arriagada R, Bergman B, Dunant A. et al. Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer. N Engl J Med 2004; 350: 351-360 https://pubmed.ncbi.nlm.nih.gov/14736927/
- 193 Salazar M, Rosen J, Wang Z. et al. Association of Delayed Adjuvant Chemotherapy With Survival After Lung Cancer Surgery. JAMA Oncol 2017; 3: 610-619 https://pubmed.ncbi.nlm.nih.gov/28056112/
- 194 Douillard JY, Rosell R, De Lena M. et al. Adjuvant vinorelbine plus cisplatin versus observation in patients with completely resected stage IB-IIIA non-small-cell lung cancer (Adjuvant Navelbine International Trialist Association [ANITA]): a randomised controlled trial. Lancet Oncol 2006; 7: 719-727 https://www.ncbi.nlm.nih.gov/pubmed/16945766
- 195 Kenmotsu H, Yamamoto N, Yamanaka T. et al. Randomized phase III study of pemetrexed/cisplatin (Pem/Cis) versus vinorelbine/cisplatin (Vnr/Cis) for completely resected stage II-IIIA non-squamous non-small-cell lung cancer (Ns-NSCLC): The JIPANG study. Journal of Clinical Oncology 2019; 37: 8501 https://doi.org/10.1200/JCO.2019.37.15_suppl.8501
- 196 Wu Y, Tsuboi M, He J. et al. Osimertinib in Resected. N Engl J Med 2020; 383: 1711-1723 https://pubmed.ncbi.nlm.nih.gov/32955177/
- 197 Felip E, Altorki N, Zhou C. et al. Adjuvant atezolizumab after adjuvant chemotherapy in resected stage IB-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase 3 trial. Lancet 2021; 398: 1344-1357 https://pubmed.ncbi.nlm.nih.gov/34555333/
- 198 Arriagada R, Bergman B, Dunant A. et al. Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer. N Engl J Med 2004; 350: 351-360 https://www.ncbi.nlm.nih.gov/pubmed/14736927
- 199 Sirzen F, Kjellen E, Sorenson S. et al. A systematic overview of radiation therapy effects in non-small cell lung cancer. Acta Oncol 2003; 42: 493-515 https://www.ncbi.nlm.nih.gov/pubmed/14596509
- 200 Bradley JD, Paulus R, Graham MV. et al. Phase II trial of postoperative adjuvant paclitaxel/carboplatin and thoracic radiotherapy in resected stage II and IIIA non-small-cell lung cancer: promising long-term results of the Radiation Therapy Oncology Group – RTOG 9705. J Clin Oncol 2005; 23: 3480-3487 https://www.ncbi.nlm.nih.gov/pubmed/15908657
- 201 Dautzenberg B, Chastang C, Arriagada R. et al. Adjuvant radiotherapy versus combined sequential chemotherapy followed by radiotherapy in the treatment of resected nonsmall cell lung carcinoma A randomized trial of 267 patients GETCB (Groupe d’Etude et de Traitement des Cancers Bronchiques). Cancer 1995; 76: 779-786 https://www.ncbi.nlm.nih.gov/pubmed/8625180
- 202 Wakelee HA, Stephenson P, Keller SM. et al. Post-operative radiotherapy (PORT) or chemoradiotherapy (CPORT) following resection of stages II and IIIA non-small cell lung cancer (NSCLC) does not increase the expected risk of death from intercurrent disease (DID) in Eastern Cooperative Oncology Group (ECOG) trial E3590. Lung Cancer 2005; 48: 389-397 https://www.ncbi.nlm.nih.gov/pubmed/15893008
- 203 Trodella L, Granone P, Valente S. et al. Adjuvant radiotherapy in non-small cell lung cancer with pathological stage I: definitive results of a phase III randomized trial. Radiother Oncol 2002; 62: 11-19 https://www.ncbi.nlm.nih.gov/pubmed/11830308
- 204 van Meerbeeck JP, Kramer GW, Van Schil PE. et al. Randomized controlled trial of resection versus radiotherapy after induction chemotherapy in stage IIIA-N2 non-small-cell lung cancer. J Natl Cancer Inst 2007; 99: 442-450 https://www.ncbi.nlm.nih.gov/pubmed/17374834
- 205 Sawyer TE, Bonner JA, Gould PM. et al. Effectiveness of postoperative irradiation in stage IIIA non-small cell lung cancer according to regression tree analyses of recurrence risks. Ann Thorac Surg 1997; 64: 1402-1407 https://www.ncbi.nlm.nih.gov/pubmed/9386711
- 206 Buderi S, Shackcloth M, Woolley S. Does induction chemoradiotherapy increase survival in patients with Pancoast tumour?. Interact Cardiovasc Thorac Surg 2016; 23: 821-825 https://pubmed.ncbi.nlm.nih.gov/27365009/
- 207 Rusch VW, Giroux DJ, Kraut MJ. et al. Induction chemoradiation and surgical resection for superior sulcus non-small-cell lung carcinomas: long-term results of Southwest Oncology Group Trial 9416 (Intergroup Trial 0160). J Clin Oncol 2007; 25: 313-318 https://www.ncbi.nlm.nih.gov/pubmed/17235046
- 208 Antonia SJ, Villegas A, Daniel D. et al. Overall Survival with Durvalumab after Chemoradiotherapy in Stage III NSCLC. N Engl J Med 2018; 379: 2342-2350
- 209 Detterbeck F, Boffa D, Kim A. et al. The Eighth Edition Lung Cancer Stage Classification. Chest 2017; 151: 193-203 https://pubmed.ncbi.nlm.nih.gov/27780786/
- 210 Andre F, Grunenwald D, Pignon J. et al. Survival of patients with resected N2 non-small-cell lung cancer: evidence for a subclassification and implications. J Clin Oncol 2000; 18: 2981-2989 https://pubmed.ncbi.nlm.nih.gov/10944131/
- 211 Asamura H, Chansky K, Crowley J. et al. The International Association for the Study of Lung Cancer Lung Cancer Staging Project: Proposals for the Revision of the N Descriptors in the Forthcoming 8th Edition of the TNM Classification for Lung Cancer. J Thorac Oncol 2015; 10: 1675-1684 https://pubmed.ncbi.nlm.nih.gov/26709477/
- 212 Goldstraw P, Chansky K, Crowley J. et al. The IASLC Lung Cancer Staging Project: Proposals for Revision of the TNM Stage Groupings in the Forthcoming (Eighth) Edition of the TNM Classification for Lung Cancer. J Thorac Oncol 2016; 11: 39-51 https://www.ncbi.nlm.nih.gov/pubmed/26762738
- 213 Faivre-Finn C, Vicente D, Kurata T. et al. Four-Year Survival With Durvalumab After Chemoradiotherapy in Stage III NSCLC-an Update From the PACIFIC Trial. J Thorac Oncol 2021; 16: 860-867 https://pubmed.ncbi.nlm.nih.gov/33476803/
- 214 Paz-Ares L, Spira A, Raben D. et al. Outcomes with durvalumab by tumour PD-L1 expression in unresectable, stage III non-small-cell lung cancer in the PACIFIC trial. Ann Oncol 2020; 31: 798-806 https://pubmed.ncbi.nlm.nih.gov/32209338/
- 215 Antonia S, Villegas A, Daniel D. et al. Overall Survival with Durvalumab after Chemoradiotherapy in Stage III NSCLC. N Engl J Med 2018; 379: 2342-2350 https://pubmed.ncbi.nlm.nih.gov/30280658/
- 216 Hui R, Özgüroğlu M, Villegas A. et al. Patient-reported outcomes with durvalumab after chemoradiotherapy in stage III, unresectable non-small-cell lung cancer (PACIFIC): a randomised, controlled, phase 3 study. Lancet Oncol 2019; 20: 1670-1680 https://pubmed.ncbi.nlm.nih.gov/31601496/
- 217 Goss G, O’Callaghan C, Lorimer I. et al. Gefitinib versus placebo in completely resected non-small-cell lung cancer: results of the NCIC CTG BR19 study. J Clin Oncol 2013; 31: 3320-3326 https://pubmed.ncbi.nlm.nih.gov/23980091/
- 218 Tsuboi M, Kato H, Nagai K. et al. Gefitinib in the adjuvant setting: safety results from a phase III study in patients with completely resected non-small cell lung cancer. Anticancer Drugs 2005; 16: 1123-1128 https://pubmed.ncbi.nlm.nih.gov/16222155/
- 219 Pennell N, Neal J, Chaft J. et al. SELECT: A Phase II Trial of Adjuvant Erlotinib in Patients With Resected Epidermal Growth Factor Receptor-Mutant Non-Small-Cell Lung Cancer. J Clin Oncol 2019; 37: 97-104 https://pubmed.ncbi.nlm.nih.gov/30444685/
- 220 D’Angelo S, Janjigian Y, Ahye N. et al. Distinct clinical course of EGFR-mutant resected lung cancers: results of testing of 1118 surgical specimens and effects of adjuvant gefitinib and erlotinib. J Thorac Oncol 2012; 7: 1815-1822 https://pubmed.ncbi.nlm.nih.gov/23154553/
- 221 Janjigian Y, Park B, Zakowski M. et al. Impact on disease-free survival of adjuvant erlotinib or gefitinib in patients with resected lung adenocarcinomas that harbor EGFR mutations. J Thorac Oncol 2011; 6: 569-575 https://pubmed.ncbi.nlm.nih.gov/21150674/
- 222 Kelly K, Altorki N, Eberhardt W. et al. Adjuvant Erlotinib Versus Placebo in Patients With Stage IB-IIIA Non-Small-Cell Lung Cancer (RADIANT): A Randomized, Double-Blind, Phase III Trial. J Clin Oncol 2015; 33: 4007-4014 https://pubmed.ncbi.nlm.nih.gov/26324372/
- 223 Zhong W, Wang Q, Mao W. et al. Gefitinib versus vinorelbine plus cisplatin as adjuvant treatment for stage II-IIIA (N1-N2) EGFR-mutant NSCLC (ADJUVANT/CTONG1104): a randomised, open-label, phase 3 study. Lancet Oncol 2018; 19: 139-148 https://pubmed.ncbi.nlm.nih.gov/29174310/
- 224 Jelinek M, Aggarwal C. Adjuvant Osimertinib: A New Standard of Care. Oncologist 2021; 26: 263-265 https://pubmed.ncbi.nlm.nih.gov/33301209/
- 225 Korevaar D, Crombag L, Cohen J. et al. Added value of combined endobronchial and oesophageal endosonography for mediastinal nodal staging in lung cancer: a systematic review and meta-analysis. Lancet Respir Med 2016; 4: 960-968 https://pubmed.ncbi.nlm.nih.gov/27773666/
- 226 Schmidt-Hansen M, Baldwin D, Hasler E. et al. PET-CT for assessing mediastinal lymph node involvement in patients with suspected resectable non-small cell lung cancer. Cochrane Database Syst Rev 2014; CD009519 https://pubmed.ncbi.nlm.nih.gov/25393718/
- 227 Eberhardt W, De Ruysscher D, Weder W. et al. 2nd ESMO Consensus Conference in Lung Cancer: locally advanced stage III non-small-cell lung cancer. Ann Oncol 2015; 26: 1573-1588 https://pubmed.ncbi.nlm.nih.gov/25897013/
- 228 Waller D, Peake M, Stephens R. et al. Chemotherapy for patients with non-small cell lung cancer: the surgical setting of the Big Lung Trial. Eur J Cardiothorac Surg 2004; 26: 173-82 https://pubmed.ncbi.nlm.nih.gov/15200998/
- 229 Strauss G, Herndon J, Maddaus M. et al. Adjuvant paclitaxel plus carboplatin compared with observation in stage IB non-small-cell lung cancer: CALGB 9633 with the Cancer and Leukemia Group B, Radiation Therapy Oncology Group, and North Central Cancer Treatment Group Study Groups. J Clin Oncol 2008; 26: 5043-5051 https://pubmed.ncbi.nlm.nih.gov/18809614/
- 230 Salazar M, Rosen J, Wang Z. et al. Association of Delayed Adjuvant Chemotherapy With Survival After Lung Cancer Surgery. JAMA Oncol 2017; 3: 610-619 https://pubmed.ncbi.nlm.nih.gov/28056112/
- 231 Sonobe M, Yamada T, Sato M. et al. Identification of subsets of patients with favorable prognosis after recurrence in completely resected non-small cell lung cancer. Ann Surg Oncol 2014; 21: 2546-2554 https://pubmed.ncbi.nlm.nih.gov/24633668/
- 232 Scagliotti GV, Fossati R, Torri V. et al. Randomized study of adjuvant chemotherapy for completely resected stage I, II, or IIIA non-small-cell Lung cancer. J Natl Cancer Inst 2003; 95: 1453-1461 https://www.ncbi.nlm.nih.gov/pubmed/14519751
- 233 Winton T, Livingston R, Johnson D. et al. Vinorelbine plus cisplatin vs observation in resected non-small-cell lung cancer. N Engl J Med 2005; 352: 2589-2597 https://www.ncbi.nlm.nih.gov/pubmed/15972865
- 234 Pignon JP, Tribodet H, Scagliotti GV. et al. Lung adjuvant cisplatin evaluation: a pooled analysis by the LACE Collaborative Group. J Clin Oncol 2008; 26: 3552-3559 https://www.ncbi.nlm.nih.gov/pubmed/18506026
- 235 Tachihara M, Dokuni R, Okuno K. et al. Phase II study of adjuvant chemotherapy with pemetrexed and cisplatin with a short hydration method for completely resected nonsquamous non-small cell lung cancer. Thorac Cancer 2020; 11: 2536-2541 https://pubmed.ncbi.nlm.nih.gov/32729237/
- 236 Kreuter M, Vansteenkiste J, Griesinger F. et al. Trial on refinement of early stage non-small cell lung cancer Adjuvant chemotherapy with pemetrexed and cisplatin versus vinorelbine and cisplatin: the TREAT protocol. BMC Cancer 2007; 7: 77 https://pubmed.ncbi.nlm.nih.gov/17488518/
- 237 Hainsworth J, Williams S, Einhorn L. et al. Successful treatment of resistant germinal neoplasms with VP-16 and cisplatin: results of a Southeastern Cancer Study Group trial. J Clin Oncol 1985; 3: 666-671 https://pubmed.ncbi.nlm.nih.gov/2582097/
- 238 McHugh D, Funt S, Silber D. et al. Adjuvant Chemotherapy With Etoposide Plus Cisplatin for Patients With Pathologic Stage II Nonseminomatous Germ Cell Tumors. J Clin Oncol 2020; 38: 1332-1337 https://pubmed.ncbi.nlm.nih.gov/32109195/
- 239 Stupp R, Mayer M, Kann R. et al. Neoadjuvant chemotherapy and radiotherapy followed by surgery in selected patients with stage IIIB non-small-cell lung cancer: a multicentre phase II trial. Lancet Oncol 2009; 10: 785-793 https://pubmed.ncbi.nlm.nih.gov/19604722/
- 240 Eberhardt W, Gauler T, Lepechoux C. et al. 10-year long-term survival (LTS) of induction chemotherapy with three cycles cisplatin/paclitaxel followed by concurrent chemoradiation cisplatin/etoposide/45 Gy (15 Gy bid) plus surgery in locally advanced non-small-cell lung cancer (NSCLC)-a multicenter phase-II trial (CISTAXOL). Lung Cancer 2013; 82: 83-89 https://pubmed.ncbi.nlm.nih.gov/23957964/
- 241 Metzenmacher M, Kopp H, Griesinger F. et al. A randomized, multicenter phase II study comparing efficacy, safety and tolerability of two dosing regimens of cisplatin and pemetrexed in patients with advanced or metastatic non-small-cell lung cancer. Ther Adv Med Oncol 2021; 13: 1758835921996506 https://pubmed.ncbi.nlm.nih.gov/34104223/
- 242 Borner M, Joncourt F, Hotz M. Similarity of apoptosis induction by 2-chlorodeoxyadenosine and cisplatin in human mononuclear blood cells. Br J Cancer 1997; 76: 1448-1454 https://pubmed.ncbi.nlm.nih.gov/9400941/
- 243 de Vries G, Rosas-Plaza X, van Vugt M. et al. Testicular cancer: Determinants of cisplatin sensitivity and novel therapeutic opportunities. Cancer Treat Rev 2020; 88: 102054 https://pubmed.ncbi.nlm.nih.gov/32593915/
- 244 Feldman D, Bosl G, Sheinfeld J. et al. Medical treatment of advanced testicular cancer. JAMA 2008; 299: 672-684 https://pubmed.ncbi.nlm.nih.gov/18270356/
- 245 Einhorn L, Donohue J. Cis-diamminedichloroplatinum, vinblastine, and bleomycin combination chemotherapy in disseminated testicular cancer. Ann Intern Med 1977; 87: 293-298 https://pubmed.ncbi.nlm.nih.gov/71004/
- 246 Osieka R, Bruntsch U, Gallmeier W. et al. [cis-Diamino-dichloro-platinum (II) in the treatment of otherwise treatment-resistant malignant testicular teratoma (author’s transl)]. Dtsch Med Wochenschr 1976; 101: 191-195 199 https://pubmed.ncbi.nlm.nih.gov/1248396/
- 247 Eberhardt W, Pöttgen C, Gauler T. et al. Phase III Study of Surgery Versus Definitive Concurrent Chemoradiotherapy Boost in Patients With Resectable Stage IIIA(N2) and Selected IIIB Non-Small-Cell Lung Cancer After Induction Chemotherapy and Concurrent Chemoradiotherapy (ESPATUE). J Clin Oncol 2015; 33: 4194-4201 https://pubmed.ncbi.nlm.nih.gov/26527789/
- 248 Einhorn L, Rapoport B, Navari R. et al. 2016 updated MASCC/ESMO consensus recommendations: prevention of nausea and vomiting following multiple-day chemotherapy, high-dose chemotherapy, and breakthrough nausea and vomiting. Support Care Cancer 2017; 25: 303-308 https://pubmed.ncbi.nlm.nih.gov/27815710/
- 249 Turrisi AT, Kim K, Blum R. et al. Twice-daily compared with once-daily thoracic radiotherapy in limited small-cell lung cancer treated concurrently with cisplatin and etoposide. N Engl J Med 1999; 340: 265-271 https://www.ncbi.nlm.nih.gov/pubmed/9920950
- 250 Wakelee HA, Dahlberg SE, Keller SM. et al. Adjuvant chemotherapy with or without bevacizumab in patients with resected non-small-cell lung cancer (E1505): an open-label, multicentre, randomised, phase 3 trial. Lancet Oncol 2017; 18: 1610-1623 https://www.ncbi.nlm.nih.gov/pubmed/29129443
- 251 Betticher DC, Hsu Schmitz SF, Totsch M. et al. Mediastinal lymph node clearance after docetaxel-cisplatin neoadjuvant chemotherapy is prognostic of survival in patients with stage IIIA pN2 non-small-cell lung cancer: a multicenter phase II trial. J Clin Oncol 2003; 21: 1752-1759 https://www.ncbi.nlm.nih.gov/pubmed/12721251
- 252 Eberhardt W, Wilke H, Stamatis G. et al. Preoperative chemotherapy followed by concurrent chemoradiation therapy based on hyperfractionated accelerated radiotherapy and definitive surgery in locally advanced non-small-cell lung cancer: mature results of a phase II trial. J Clin Oncol 1998; 16: 622-634 https://www.ncbi.nlm.nih.gov/pubmed/9469351
- 253 Ardizzoni A, Boni L, Tiseo M. et al. Cisplatin- versus carboplatin-based chemotherapy in first-line treatment of advanced non-small-cell lung cancer: an individual patient data meta-analysis. J Natl Cancer Inst 2007; 99: 847-857 https://www.ncbi.nlm.nih.gov/pubmed/17551145
- 254 Yuan M, Men Y, Kang J. et al. Postoperative radiotherapy for pathological stage IIIA-N2 non-small cell lung cancer with positive surgical margins. Thorac Cancer 2021; 12: 227-234 https://pubmed.ncbi.nlm.nih.gov/33247556/
- 255 Edwards J, Chansky K, Van Schil P. et al. The IASLC Lung Cancer Staging Project: Analysis of Resection Margin Status and Proposals for Residual Tumor Descriptors for Non-Small Cell Lung Cancer. J Thorac Oncol 2020; 15: 344-359 https://pubmed.ncbi.nlm.nih.gov/31731014/
- 256 Gu C, Wang R, Pan X. et al. Comprehensive study of prognostic risk factors of patients underwent pneumonectomy. J Cancer 2017; 8: 2097-2103 https://pubmed.ncbi.nlm.nih.gov/28819411/
- 257 Petrella F, Spaggiari L. Therapeutic options following pneumonectomy in non-small cell lung cancer. Expert Rev Respir Med 2016; 10: 919-925 https://pubmed.ncbi.nlm.nih.gov/27176616/
- 258 Brandt W, Yan W, Leeman J. et al. Postoperative Radiotherapy for Surgically Resected ypN2 Non-Small Cell Lung Cancer. Ann Thorac Surg 2018; 106: 848-855 https://pubmed.ncbi.nlm.nih.gov/29807005/
- 259 Francis S, Orton A, Stoddard G. et al. Sequencing of Postoperative Radiotherapy and Chemotherapy for Locally Advanced or Incompletely Resected Non-Small-Cell Lung Cancer. J Clin Oncol 2018; 36: 333-341 https://pubmed.ncbi.nlm.nih.gov/29236592/
- 260 Weder W, Collaud S, Eberhardt W. et al. Pneumonectomy is a valuable treatment option after neoadjuvant therapy for stage III non-small-cell lung cancer. J Thorac Cardiovasc Surg 2010; 139: 1424-1430 https://pubmed.ncbi.nlm.nih.gov/20416887/
- 261 Shepherd A, Iocolano M, Leeman J. et al. Clinical and Dosimetric Predictors of Radiation Pneumonitis in Patients With Non-Small Cell Lung Cancer Undergoing Postoperative Radiation Therapy. Pract Radiat Oncol 2021; 11: e52-e62 https://pubmed.ncbi.nlm.nih.gov/33068790/
- 262 Paumier A, Le Péchoux C. Post-operative radiation therapy. Transl Lung Cancer Res 2013; 2: 423-432 https://pubmed.ncbi.nlm.nih.gov/25806262/
- 263 Dienemann H, Trainer C, Hoffmann H. et al. [Incomplete resections in bronchial carcinoma: morbidity and prognosis]. Chirurg 1997; 68: 1014-1019
- 264 Robert Koch-Institut (RKI). Bericht zum Krebsgeschen in Deutschland 2016. 2016 https://www.krebsdaten.de/Krebs/DE/Content/Publikationen/Krebsgeschehen/Krebsgeschehen_download.pdf?__blob=publicationFile
- 265 Stamatis G, Djuric D, Eberhardt W. et al. Postoperative morbidity and mortality after induction chemoradiotherapy for locally advanced lung cancer: an analysis of 350 operated patients. Eur J Cardiothorac Surg 2002; 22: 292-297 https://www.ncbi.nlm.nih.gov/pubmed/12142202
- 266 Wu S, Shaikh F, Cerfolio R. et al. PORT in Properly Selected Patients With Completely Resected Non-Small Cell Lung Cancer Should Not Be Quickly Dismissed. Ann Thorac Surg 2019; 107: 1585-1586 https://pubmed.ncbi.nlm.nih.gov/30447194/
- 267 Douillard J, Rosell R, De Lena M. et al. Impact of postoperative radiation therapy on survival in patients with complete resection and stage I, II, or IIIA non-small-cell lung cancer treated with adjuvant chemotherapy: the adjuvant Navelbine International Trialist Association (ANITA) Randomized Trial. Int J Radiat Oncol Biol Phys 2008; 72: 695-701 https://pubmed.ncbi.nlm.nih.gov/18439766/
- 268 Robinson C, Patel A, Bradley J. et al. Postoperative radiotherapy for pathologic N2 non-small-cell lung cancer treated with adjuvant chemotherapy: a review of the National Cancer Data Base. J Clin Oncol 2015; 33: 870-876 https://pubmed.ncbi.nlm.nih.gov/25667283/
- 269 Péchoux C, Mercier O, Belemsagha D. et al. Role of adjuvant radiotherapy in completely resected non-small-cell lung cancer. EJC Suppl 2013; 11: 123-130 https://pubmed.ncbi.nlm.nih.gov/26217121/
- 270 Le Pechoux C, Pourel N, Barlesi F. et al. LBA3_PR An international randomized trial, comparing post-operative conformal radiotherapy (PORT) to no PORT, in patients with completely resected non-small cell lung cancer (NSCLC) and mediastinal N2 involvement: Primary end-point analysis of LungART (IFCT-0503, UK NCRI, SAKK) NCT00410683. Annals of Oncology 2020; 31: S1178 https://doi.org/10.1016/j.annonc.2020.08.2280
- 271 PORT Meta-analysis Trialists Group. Postoperative radiotherapy in non-small-cell lung cancer: systematic review and meta-analysis of individual patient data from nine randomised controlled trials PORT Meta-analysis Trialists Group. Lancet 1998; 352: 257-263 https://pubmed.ncbi.nlm.nih.gov/9690404/
- 272 Lally BE, Zelterman D, Colasanto JM. et al. Postoperative radiotherapy for stage II or III non-small-cell lung cancer using the surveillance, epidemiology, and end results database. J Clin Oncol 2006; 24: 2998-3006 https://www.ncbi.nlm.nih.gov/pubmed/16769986
- 273 Farray D, Mirkovic N, Albain K. Multimodality therapy for stage III non-small-cell lung cancer. J Clin Oncol 2005; 23: 3257-3269 https://pubmed.ncbi.nlm.nih.gov/15886313/
- 274 Pless M, Stupp R, Ris H. et al. Induction chemoradiation in stage IIIA/N2 non-small-cell lung cancer: a phase 3 randomised trial. Lancet 2015; 386: 1049-1056 https://pubmed.ncbi.nlm.nih.gov/26275735/
- 275 Pöttgen C, Eberhardt W, Stamatis G. et al. Definitive radiochemotherapy versus surgery within multimodality treatment in stage III non-small cell lung cancer (NSCLC) – a cumulative meta-analysis of the randomized evidence. Oncotarget 2017; 8: 41670-41678 https://pubmed.ncbi.nlm.nih.gov/28415831/
- 276 Pöttgen C, Gauler T, Bellendorf A. et al. Standardized Uptake Decrease on [18F]-Fluorodeoxyglucose Positron Emission Tomography After Neoadjuvant Chemotherapy Is a Prognostic Classifier for Long-Term Outcome After Multimodality Treatment: Secondary Analysis of a Randomized Trial for Resectable Stage IIIA/B Non-Small-Cell Lung Cancer. J Clin Oncol 2016; 34: 2526-2533 https://pubmed.ncbi.nlm.nih.gov/27247220/
- 277 Früh M, Betticher D, Stupp R. et al. Multimodal Treatment in Operable Stage III NSCLC: A Pooled Analysis on Long-Term Results of Three SAKK trials (SAKK 16/96, 16/00, and 16/01). J Thorac Oncol 2019; 14: 115-123 https://pubmed.ncbi.nlm.nih.gov/30267838/
- 278 Pezzetta E, Stupp R, Zouhair A. et al. Comparison of neoadjuvant cisplatin-based chemotherapy versus radiochemotherapy followed by resection for stage III (N2) NSCLC. Eur J Cardiothorac Surg 2005; 27: 1092-1098 https://pubmed.ncbi.nlm.nih.gov/15896624/
- 279 Vansteenkiste J, De Ruysscher D, Eberhardt W. et al. Early and locally advanced non-small-cell lung cancer (NSCLC): ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2013; 24 (Suppl. 06) vi89-v98 https://pubmed.ncbi.nlm.nih.gov/23860613/
- 280 Pöttgen C, Eberhardt W, Bildat S. et al. Induction chemotherapy followed by concurrent chemotherapy and definitive high-dose radiotherapy for patients with locally advanced non-small-cell lung cancer (stages IIIa/IIIb): a pilot phase I/II trial. Ann Oncol 2002; 13: 403-411 https://pubmed.ncbi.nlm.nih.gov/11996471/
- 281 Eberhardt W, Stamatis G, Stuschke M. Surgery in stage III non-small-cell lung cancer. Lancet 2009; 374: 359-360 https://pubmed.ncbi.nlm.nih.gov/19632715/
- 282 Junker K, Langner K, Klinke F. et al. Grading of tumor regression in non-small cell lung cancer : morphology and prognosis. Chest 2001; 120: 1584-1591 https://pubmed.ncbi.nlm.nih.gov/11713138/
- 283 Van Schil P, Van Meerbeeck J, Kramer G. et al. Morbidity and mortality in the surgery arm of EORTC 08941 trial. Eur Respir J 2005; 26: 192-197 https://pubmed.ncbi.nlm.nih.gov/16055865/
- 284 Senan S, Brade A, Wang L. et al. PROCLAIM: Randomized Phase III Trial of Pemetrexed-Cisplatin or Etoposide-Cisplatin Plus Thoracic Radiation Therapy Followed by Consolidation Chemotherapy in Locally Advanced Nonsquamous Non-Small-Cell Lung Cancer. J Clin Oncol 2016; 34: 953-962 https://pubmed.ncbi.nlm.nih.gov/26811519/
- 285 Decaluwé H, De Leyn P, Vansteenkiste J. et al. Surgical multimodality treatment for baseline resectable stage IIIA-N2 non-small cell lung cancer Degree of mediastinal lymph node involvement and impact on survival. Eur J Cardiothorac Surg 2009; 36: 433-439 https://pubmed.ncbi.nlm.nih.gov/19502079/
- 286 Behera M, Steuer C, Liu Y. et al. Trimodality Therapy in the Treatment of Stage III N2-Positive Non-Small Cell Lung Cancer: A National Cancer Database Analysis. Oncologist 2020; 25: e964-e975 https://pubmed.ncbi.nlm.nih.gov/31943520/
- 287 Friedel G, Budach W, Dippon J. et al. Phase II trial of a trimodality regimen for stage III non-small-cell lung cancer using chemotherapy as induction treatment with concurrent hyperfractionated chemoradiation with carboplatin and paclitaxel followed by subsequent resection: a single-center study. J Clin Oncol 2010; 28: 942-948 https://pubmed.ncbi.nlm.nih.gov/20100967/
- 288 Thomas M, Rube C, Semik M. et al. Impact of preoperative bimodality induction including twice-daily radiation on tumor regression and survival in stage III non-small-cell lung cancer. J Clin Oncol 1999; 17: 1185 https://www.ncbi.nlm.nih.gov/pubmed/10561177
- 289 Albain KS, Swann RS, Rusch VW. et al. Radiotherapy plus chemotherapy with or without surgical resection for stage III non-small-cell lung cancer: a phase III randomised controlled trial. Lancet 2009; 374: 379-386 https://www.ncbi.nlm.nih.gov/pubmed/19632716
- 290 Friedel G, Hruska D, Budach W. et al. Neoadjuvant chemoradiotherapy of stage III non-small-cell lung cancer. Lung Cancer 2000; 30: 175-185 https://www.ncbi.nlm.nih.gov/pubmed/11137202
- 291 Dillman RO, Herndon J, Seagren SL. et al. Improved survival in stage III non-small-cell lung cancer: seven-year follow-up of cancer and leukemia group B (CALGB) 8433 trial. J Natl Cancer Inst 1996; 88: 1210-1215 https://www.ncbi.nlm.nih.gov/pubmed/8780630
- 292 Le CT, Arriagada R, Quoix E. et al. Radiotherapy alone versus combined chemotherapy and radiotherapy in unresectable non-small cell lung carcinoma. Lung Cancer 1994; 10 (Suppl. 01) S239-S244 https://www.ncbi.nlm.nih.gov/pubmed/8087515
- 293 Sause W, Kolesar P, Taylor SI. et al. Final results of phase III trial in regionally advanced unresectable non-small cell lung cancer: Radiation Therapy Oncology Group, Eastern Cooperative Oncology Group, and Southwest Oncology Group. Chest 2000; 117: 358-364 https://www.ncbi.nlm.nih.gov/pubmed/10669675
- 294 Pottgen C, Eberhardt W, Grannass A. et al. Prophylactic cranial irradiation in operable stage IIIA non small-cell lung cancer treated with neoadjuvant chemoradiotherapy: results from a German multicenter randomized trial. J Clin Oncol 2007; 25: 4987-4992
- 295 Hainsworth J, Waterhouse D, Shih K. et al. Phase II trial of preoperative pemetrexed plus carboplatin in patients with stage IB-III nonsquamous non-small cell lung cancer (NSCLC). Lung Cancer 2018; 118: 6-12 https://pubmed.ncbi.nlm.nih.gov/29572004/
- 296 Masters G, Wang X, Hodgson L. et al. A phase II trial of high dose carboplatin and paclitaxel with G-CSF and peripheral blood stem cell support followed by surgery and/or chest radiation in patients with stage III non-small cell lung cancer: CALGB 9531. Lung Cancer 2011; 74: 258-263 https://pubmed.ncbi.nlm.nih.gov/21529989/
- 297 De Candis D, Stani S, Bidoli P. et al. Induction chemotherapy with carboplatin/paclitaxel followed by surgery or standard radiotherapy and concurrent daily low-dose cisplatin for locally advanced non-small cell lung cancer (NSCLC). Am J Clin Oncol 2003; 26: 265-269 https://pubmed.ncbi.nlm.nih.gov/12796598/
- 298 Vokes EE, Herndon JE, Kelley MJ. et al. Induction chemotherapy followed by chemoradiotherapy compared with chemoradiotherapy alone for regionally advanced unresectable stage III Non-small-cell lung cancer: Cancer and Leukemia Group B. J Clin Oncol 2007; 25: 1698-1704 https://www.ncbi.nlm.nih.gov/pubmed/17404369
- 299 Chun S, Hu C, Choy H. et al. Impact of Intensity-Modulated Radiation Therapy Technique for Locally Advanced Non-Small-Cell Lung Cancer: A Secondary Analysis of the NRG Oncology RTOG 0617 Randomized Clinical Trial. J Clin Oncol 2017; 35: 56-62 https://pubmed.ncbi.nlm.nih.gov/28034064/
- 300 Chiappetta M, Leuzzi G, Sperduti I. et al. Mediastinal Up-Staging During Surgery in Non-Small-Cell Lung Cancer: Which Mediastinal Lymph Node Metastasis Patterns Better Predict The Outcome? A Multicenter Analysis. Clin Lung Cancer 2020; 21: 464-471.e1 https://pubmed.ncbi.nlm.nih.gov/32389508/
- 301 Shang X, Li Z, Lin J. et al. Incorporating the Number of PLN into the AJCC Stage Could Better Predict the Survival for Patients with NSCLC: A Large Population-Based Study. Journal of Oncology 2020; 2020: 1087237 https://doi.org/10.1155/2020/1087237
- 302 Osarogiagbon R, Faris N, Stevens W. et al. Beyond Margin Status: Population-Based Validation of the Proposed International Association for the Study of Lung Cancer Residual Tumor Classification Recategorization. J Thorac Oncol 2020; 15: 371-382 https://pubmed.ncbi.nlm.nih.gov/31783180/
- 303 Sun X, Men Y, Wang J. et al. Risk of cardiac-related mortality in stage IIIA-N2 non-small cell lung cancer: Analysis of the Surveillance, Epidemiology, and End Results (SEER) database. Thorac Cancer 2021; 12: 1358-1365 https://pubmed.ncbi.nlm.nih.gov/33728811/
- 304 Arriagada R, Dunant A, Pignon J. et al. Long-term results of the international adjuvant lung cancer trial evaluating adjuvant Cisplatin-based chemotherapy in resected lung cancer. J Clin Oncol 2010; 28: 35-42 https://pubmed.ncbi.nlm.nih.gov/19933916/
- 305 Billiet C, De Ruysscher D, Peeters S. et al. Patterns of Locoregional Relapses in Patients with Contemporarily Staged Stage III-N2 NSCLC Treated with Induction Chemotherapy and Resection: Implications for Postoperative Radiotherapy Target Volumes. J Thorac Oncol 2016; 11: 1538-1549 https://pubmed.ncbi.nlm.nih.gov/27374454/
- 306 Burdett S, Rydzewska L, Tierney J. et al. Postoperative radiotherapy for non-small cell lung cancer. Cochrane Database Syst Rev 2016; 10: CD002142 https://pubmed.ncbi.nlm.nih.gov/27727451/
- 307 Sun J, Noh J, Oh D. et al. Randomized Phase II Trial Comparing Chemoradiotherapy with Chemotherapy for Completely Resected Unsuspected N2-Positive Non-Small Cell Lung Cancer. J Thorac Oncol 2017; 12: 1806-1813 https://pubmed.ncbi.nlm.nih.gov/28962948/
- 308 Shen W, Ji J, Zuo Y. et al. Comparison of efficacy for postoperative chemotherapy and concurrent radiochemotherapy in patients with IIIA-pN2 non-small cell lung cancer: an early closed randomized controlled trial. Radiother Oncol 2014; 110: 120-125 https://pubmed.ncbi.nlm.nih.gov/24183868/
- 309 Billiet C, Decaluwé H, Peeters S. et al. Modern post-operative radiotherapy for stage III non-small cell lung cancer may improve local control and survival: a meta-analysis. Radiother Oncol 2014; 110: 3-8 https://pubmed.ncbi.nlm.nih.gov/24100149/
- 310 Girard N, Mornex F, Douillard J. et al. Is neoadjuvant chemoradiotherapy a feasible strategy for stage IIIA-N2 non-small cell lung cancer? Mature results of the randomized IFCT-0101 phase II trial. Lung Cancer 2010; 69: 86-93 https://pubmed.ncbi.nlm.nih.gov/19879013/
- 311 Suntharalingam M, Paulus R, Edelman M. et al. Radiation therapy oncology group protocol 02-29: a phase II trial of neoadjuvant therapy with concurrent chemotherapy and full-dose radiation therapy followed by surgical resection and consolidative therapy for locally advanced non-small cell carcinoma of the lung. Int J Radiat Oncol Biol Phys 2012; 84: 456-463 https://pubmed.ncbi.nlm.nih.gov/22543206/
- 312 Cerfolio R, Bryant A, Jones V. et al. Pulmonary resection after concurrent chemotherapy and high dose (60Gy) radiation for non-small cell lung cancer is safe and may provide increased survival. Eur J Cardiothorac Surg 2009; 35: 718-723 discussion 723 https://pubmed.ncbi.nlm.nih.gov/19233668/
- 313 Chen Y, Peng X, Zhou Y. et al. Comparing the benefits of chemoradiotherapy and chemotherapy for resectable stage III A/N2 non-small cell lung cancer: a meta-analysis. World J Surg Oncol 2018; 16: 8 https://pubmed.ncbi.nlm.nih.gov/29338734/
- 314 Pöttgen C, Stuschke M, Graupner B. et al. Prognostic model for long-term survival of locally advanced non-small-cell lung cancer patients after neoadjuvant radiochemotherapy and resection integrating clinical and histopathologic factors. BMC Cancer 2015; 15: 363 https://pubmed.ncbi.nlm.nih.gov/25943191/
- 315 Bradley J, Paulus R, Komaki R. et al. Standard-dose versus high-dose conformal radiotherapy with concurrent and consolidation carboplatin plus paclitaxel with or without cetuximab for patients with stage IIIA or IIIB non-small-cell lung cancer (RTOG 0617): a randomised, two-by-two factorial phase 3 study. Lancet Oncol 2015; 16: 187-199 https://pubmed.ncbi.nlm.nih.gov/25601342/
- 316 Bradley J, Hu C, Komaki R. et al. Long-Term Results of NRG Oncology RTOG 0617: Standard- Versus High-Dose Chemoradiotherapy With or Without Cetuximab for Unresectable Stage III Non-Small-Cell Lung Cancer. J Clin Oncol 2020; 38: 706-714 https://pubmed.ncbi.nlm.nih.gov/31841363/
- 317 Guberina N, Pöttgen C, Schuler M. et al. Comparison of early tumour-associated versus late deaths in patients with central or >7 cm T4 N0/1 M0 non-small-cell lung-cancer undergoing trimodal treatment: Only few risks left to improve. Eur J Cancer 2020; 138: 156-168 https://pubmed.ncbi.nlm.nih.gov/32889370/
- 318 Curioni-Fontecedro A, Perentes J, Gelpke H. et al. Preoperative chemotherapy and radiotherapy concomitant to cetuximab in resectable stage IIIB NSCLC: a multicentre phase 2 trial (SAKK 16/08). Br J Cancer 2019; 120: 968-974 https://pubmed.ncbi.nlm.nih.gov/30988393/
- 319 Bi N, Liu L, Liang J. et al. Efficacy and safety of concurrent chemoradiotherapy in ECOG 2 patients with locally advanced non-small-cell lung cancer: a subgroup analysis of a randomized phase III trial. BMC Cancer 2020; 20: 278 https://pubmed.ncbi.nlm.nih.gov/32252680/
- 320 Atagi S, Kawahara M, Yokoyama A. et al. Thoracic radiotherapy with or without daily low-dose carboplatin in elderly patients with non-small-cell lung cancer: a randomised, controlled, phase 3 trial by the Japan Clinical Oncology Group (JCOG0301). Lancet Oncol 2012; 13: 671-678 https://pubmed.ncbi.nlm.nih.gov/22622008/
- 321 Stinchcombe T, Zhang Y, Vokes E. et al. Pooled Analysis of Individual Patient Data on Concurrent Chemoradiotherapy for Stage III Non-Small-Cell Lung Cancer in Elderly Patients Compared With Younger Patients Who Participated in US National Cancer Institute Cooperative Group Studies. J Clin Oncol 2017; 35: 2885-2892 https://pubmed.ncbi.nlm.nih.gov/28493811/
- 322 Song W, Zhou N, Wang W. et al. Survival benefit of neoadjuvant chemotherapy in non-small cell lung cancer: an updated meta-analysis of 13 randomized control trials. J Thorac Oncol 2010; 5: 510-516 https://pubmed.ncbi.nlm.nih.gov/20107424/
- 323 Ying M, Liu J, Zhou W. et al. The Role of Additional Chemotherapy in Combination with Concurrent Chemoradiotherapy for Locally Advanced Inoperable Non-Small Cell Lung Cancer, a Systematic Review and Meta-Analysis of 12 Randomized Trials. Cancer Invest 2019; 37: 376-386 https://pubmed.ncbi.nlm.nih.gov/31474153/
- 324 Faivre-Finn C, Spigel D, Senan S. et al. Impact of prior chemoradiotherapy-related variables on outcomes with durvalumab in unresectable Stage III NSCLC (PACIFIC). Lung Cancer 2021; 151: 30-38 https://pubmed.ncbi.nlm.nih.gov/33285469/
- 325 Gebbia V, Galetta D, Riccardi F. et al. Vinorelbine plus cisplatin versus cisplatin plus vindesine and mitomycin C in stage IIIB-IV non-small cell lung carcinoma: a prospective randomized study. Lung Cancer 2002; 37: 179-187 https://pubmed.ncbi.nlm.nih.gov/12140141/
- 326 Le Chevalier T, Brisgand D, Douillard J. et al. Randomized study of vinorelbine and cisplatin versus vindesine and cisplatin versus vinorelbine alone in advanced non-small-cell lung cancer: results of a European multicenter trial including 612 patients. J Clin Oncol 1994; 12: 360-367 https://pubmed.ncbi.nlm.nih.gov/8113844/
- 327 Palma D, Senan S, Tsujino K. et al. Predicting radiation pneumonitis after chemoradiation therapy for lung cancer: an international individual patient data meta-analysis. Int J Radiat Oncol Biol Phys 2013; 85: 444-450 https://pubmed.ncbi.nlm.nih.gov/22682812/
- 328 Liu T, He Z, Dang J. et al. Comparative efficacy and safety for different chemotherapy regimens used concurrently with thoracic radiation for locally advanced non-small cell lung cancer: a systematic review and network meta-analysis. Radiat Oncol 2019; 14: 55 https://pubmed.ncbi.nlm.nih.gov/30925881/
- 329 Liang J, Bi N, Wu S. et al. Etoposide and cisplatin versus paclitaxel and carboplatin with concurrent thoracic radiotherapy in unresectable stage III non-small cell lung cancer: a multicenter randomized phase III trial. Ann Oncol 2017; 28: 777-783 https://pubmed.ncbi.nlm.nih.gov/28137739/
- 330 Curran W, Paulus R, Langer C. et al. Sequential vs concurrent chemoradiation for stage III non-small cell lung cancer: randomized phase III trial RTOG 9410. J Natl Cancer Inst 2011; 103: 1452-1460 https://pubmed.ncbi.nlm.nih.gov/21903745/
- 331 Schaake-Koning C, van den Bogaert W, Dalesio O. et al. Effects of concomitant cisplatin and radiotherapy on inoperable non-small-cell lung cancer. N Engl J Med 1992; 326: 524-530 https://www.ncbi.nlm.nih.gov/pubmed/1310160
- 332 Furuse K, Fukuoka M, Kawahara M. et al. Phase III study of concurrent versus sequential thoracic radiotherapy in combination with mitomycin, vindesine, and cisplatin in unresectable stage III non-small-cell lung cancer. J Clin Oncol 1999; 17: 2692-2699 https://www.ncbi.nlm.nih.gov/pubmed/10561343
- 333 Fournel P, Robinet G, Thomas P. et al. Randomized phase III trial of sequential chemoradiotherapy compared with concurrent chemoradiotherapy in locally advanced non-small-cell lung cancer: Groupe Lyon-Saint-Etienne d’Oncologie Thoracique-Groupe Francais de Pneumo-Cancerologie NPC 95-01 Study. J Clin Oncol 2005; 23: 5910-5917 https://www.ncbi.nlm.nih.gov/pubmed/16087956
- 334 Nestle U, Schimek-Jasch T, Kremp S. et al. Imaging-based target volume reduction in chemoradiotherapy for locally advanced non-small-cell lung cancer (PET-Plan): a multicentre, open-label, randomised, controlled trial. Lancet Oncol 2020; 21: 581-592 https://pubmed.ncbi.nlm.nih.gov/32171429/
- 335 Guberina M, Darwiche K, Hautzel H. et al. Impact of EBUS-TBNA in addition to [18F]FDG-PET/CT imaging on target volume definition for radiochemotherapy in stage III NSCLC. Eur J Nucl Med Mol Imaging 2021; 48: 2894-2903 https://pubmed.ncbi.nlm.nih.gov/33547554/
- 336 Gan Q, Stewart J, Valik E. et al. Cytologic Evaluation of Positron Emission Tomography-Computed Tomography-Positive Lymph Nodes Sampled by Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration: Experience at a Large Cancer Center. Arch Pathol Lab Med 2019; 143: 1265-1270 https://pubmed.ncbi.nlm.nih.gov/31063012/
- 337 Nestle U, De Ruysscher D, Ricardi U. et al. ESTRO ACROP guidelines for target volume definition in the treatment of locally advanced non-small cell lung cancer. Radiother Oncol 2018; 127: 1-5 https://pubmed.ncbi.nlm.nih.gov/29605476/
- 338 Zhang T, Snir J, Boldt R. et al. Is the Importance of Heart Dose Overstated in the Treatment of Non-Small Cell Lung Cancer? A Systematic Review of the Literature. Int J Radiat Oncol Biol Phys 2019; 104: 582-589 https://pubmed.ncbi.nlm.nih.gov/30630029/
- 339 Banfill K, Giuliani M, Aznar M. et al. Cardiac Toxicity of Thoracic Radiotherapy: Existing Evidence and Future Directions. J Thorac Oncol 2021; 16: 216-227 https://pubmed.ncbi.nlm.nih.gov/33278607/
- 340 Totzeck M, Schuler M, Stuschke M. et al. Cardio-oncology – strategies for management of cancer-therapy related cardiovascular disease. Int J Cardiol 2019; 280: 163-175 https://pubmed.ncbi.nlm.nih.gov/30661849/
- 341 De Ruysscher D, Faivre-Finn C, Moeller D. et al. European Organization for Research and Treatment of Cancer (EORTC) recommendations for planning and delivery of high-dose, high precision radiotherapy for lung cancer. Radiother Oncol 2017; 124: 1-10 https://pubmed.ncbi.nlm.nih.gov/28666551/
- 342 Fowler J, Chappell R. Non-small cell lung tumors repopulate rapidly during radiation therapy. Int J Radiat Oncol Biol Phys 2000; 46: 516-517 https://pubmed.ncbi.nlm.nih.gov/10661362/
- 343 Feldmann H. [Split-course radiotherapy or treatment interruption]. Strahlenther Onkol 2000; 176: 458-461 https://pubmed.ncbi.nlm.nih.gov/11068590/
- 344 Perez CA, Stanley K, Rubin P. et al. A prospective randomized study of various irradiation doses and fractionation schedules in the treatment of inoperable non-oat-cell carcinoma of the lung Preliminary report by the Radiation Therapy Oncology Group. Cancer 1980; 45: 2744-2753 https://www.ncbi.nlm.nih.gov/pubmed/6991092
- 345 Perez CA, Pajak TF, Rubin P. et al. Long-term observations of the patterns of failure in patients with unresectable non-oat cell carcinoma of the lung treated with definitive radiotherapy Report by the Radiation Therapy Oncology Group. Cancer 1987; 59: 1874-1881 https://www.ncbi.nlm.nih.gov/pubmed/3032394
- 346 Saunders M, Dische S, Barrett A. et al. Continuous, hyperfractionated, accelerated radiotherapy (CHART) versus conventional radiotherapy in non-small cell lung cancer: mature data from the randomised multicentre trial CHART Steering committee. Radiother Oncol 1999; 52: 137-148 https://www.ncbi.nlm.nih.gov/pubmed/10577699
- 347 Butts C, Socinski M, Mitchell P. et al. Tecemotide (L-BLP25) versus placebo after chemoradiotherapy for stage III non-small-cell lung cancer (START): a randomised, double-blind, phase 3 trial. Lancet Oncol 2014; 15: 59-68 https://pubmed.ncbi.nlm.nih.gov/24331154/
- 348 Huber R, Reck M, Thomas M. Current status of and future strategies for multimodality treatment of unresectable stage III nonsmall cell lung cancer. Eur Respir J 2013; 42: 1119-1133 https://pubmed.ncbi.nlm.nih.gov/23429914/
- 349 Kelly K, Chansky K, Gaspar L. et al. Phase III trial of maintenance gefitinib or placebo after concurrent chemoradiotherapy and docetaxel consolidation in inoperable stage III non-small-cell lung cancer: SWOG S0023. J Clin Oncol 2008; 26: 2450-2456 https://pubmed.ncbi.nlm.nih.gov/18378568/
- 350 Antonia S, Villegas A, Daniel D. et al. Durvalumab after Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer. N Engl J Med 2017; 377: 1919-1929 https://pubmed.ncbi.nlm.nih.gov/28885881/
- 351 Ahn J, Ahn Y, Kim J. et al. Multinational Randomized Phase III Trial With or Without Consolidation Chemotherapy Using Docetaxel and Cisplatin After Concurrent Chemoradiation in Inoperable Stage III Non-Small-Cell Lung Cancer: KCSG-LU05-04. J Clin Oncol 2015; 33: 2660-2666 https://pubmed.ncbi.nlm.nih.gov/26150444/
- 352 Hanna N, Neubauer M, Yiannoutsos C. et al. Phase III study of cisplatin, etoposide, and concurrent chest radiation with or without consolidation docetaxel in patients with inoperable stage III non-small-cell lung cancer: the Hoosier Oncology Group and US Oncology. J Clin Oncol 2008; 26: 5755-5760 https://pubmed.ncbi.nlm.nih.gov/19001323/
- 353 Gandara DR, Chansky K, Albain KS. et al. Consolidation docetaxel after concurrent chemoradiotherapy in stage IIIB non-small-cell lung cancer: phase II Southwest Oncology Group Study S9504. J Clin Oncol 2003; 21: 2004-2010 https://www.ncbi.nlm.nih.gov/pubmed/12743155
- 354 Hanna NH, Neubauer M, Ansari R. et al. Phase III trial of cisplatin (P) plus etoposide (E) plus concurrent chest radiation (XRT) with or without consolidation docetaxel (D) in patients (pts) with inoperable stage III non-small cell lung cancer (NSCLC): HOG LUN 01-24/USO-023. J Clin Oncol 2007; 25: 7512 https://www.ncbi.nlm.nih.gov/pubmed/19001323
- 355 Baker S, Dahele M, Lagerwaard F. et al. A critical review of recent developments in radiotherapy for non-small cell lung cancer. Radiat Oncol 2016; 11: 115 https://pubmed.ncbi.nlm.nih.gov/27600665/
- 356 Jumeau R, Vilotte F, Durham A. et al. Current landscape of palliative radiotherapy for non-small-cell lung cancer. Transl Lung Cancer Res 2019; 8 (Suppl. 02) S192-S201 https://pubmed.ncbi.nlm.nih.gov/31673524/
- 357 Stevens R, Macbeth F, Toy E. et al. Palliative radiotherapy regimens for patients with thoracic symptoms from non-small cell lung cancer. Cochrane Database Syst Rev 2015; 1: CD002143 https://pubmed.ncbi.nlm.nih.gov/25586198/
- 358 Fairchild A, Harris K, Barnes E. et al. Palliative thoracic radiotherapy for lung cancer: a systematic review. J Clin Oncol 2008; 26: 4001-4011 https://pubmed.ncbi.nlm.nih.gov/18711191/
- 359 Moeller B, Balagamwala E, Chen A. et al. Palliative thoracic radiation therapy for non-small cell lung cancer: 2018 Update of an American Society for Radiation Oncology (ASTRO) Evidence-Based Guideline. Pract Radiat Oncol 2018; 8: 245-250 https://pubmed.ncbi.nlm.nih.gov/29625898/
- 360 Ball D, Smith J, Bishop J. et al. A phase III study of radiotherapy with and without continuous-infusion fluorouracil as palliation for non-small-cell lung cancer. Br J Cancer 1997; 75: 690-697 https://pubmed.ncbi.nlm.nih.gov/9043026/
- 361 Nawrocki S, Krzakowski M, Wasilewska-Tesluk E. et al. Concurrent chemotherapy and short course radiotherapy in patients with stage IIIA to IIIB non-small cell lung cancer not eligible for radical treatment: results of a randomized phase II study. J Thorac Oncol 2010; 5: 1255-1262 https://pubmed.ncbi.nlm.nih.gov/20592630/
- 362 Strøm H, Bremnes R, Sundstrøm S. et al. Concurrent palliative chemoradiation leads to survival and quality of life benefits in poor prognosis stage III non-small-cell lung cancer: a randomised trial by the Norwegian Lung Cancer Study Group. Br J Cancer 2013; 109: 1467-1475 https://pubmed.ncbi.nlm.nih.gov/23963145/
- 363 Reinfuss M, Mucha-Małecka A, Walasek T. et al. Palliative thoracic radiotherapy in non-small cell lung cancer An analysis of 1250 patients Palliation of symptoms, tolerance and toxicity. Lung Cancer 2011; 71: 344-349 https://pubmed.ncbi.nlm.nih.gov/20674068/
- 364 Sezer A, Kilickap S, Gümüş M. et al. Cemiplimab monotherapy for first-line treatment of advanced non-small-cell lung cancer with PD-L1 of at least 50%: a multicentre, open-label, global, phase 3, randomised, controlled trial. Lancet 2021; 397: 592-604 https://pubmed.ncbi.nlm.nih.gov/33581821/
- 365 von Laffert M, Schirmacher P, Warth A. et al. Stellungnahme der DGP und der AG Thorakale Onkologie der AG Onkologie/Deutsche Krebsgesellschaft e. V. zur ALK-Testung beim NSCLC. Der Pathologe 2016; 37: 187-192 https://doi.org/10.1007/s00292-016-0152-1
- 366 Herbst R, Giaccone G, de Marinis F. et al. Atezolizumab for First-Line Treatment of PD-L1-Selected Patients with NSCLC. N Engl J Med 2020; 383: 1328-1339 https://pubmed.ncbi.nlm.nih.gov/32997907/
- 367 Paz-Ares L, Ciuleanu T, Cobo M. et al. First-line nivolumab plus ipilimumab combined with two cycles of chemotherapy in patients with non-small-cell lung cancer (CheckMate 9LA): an international, randomised, open-label, phase 3 trial. Lancet Oncol 2021; 22: 198-211 https://pubmed.ncbi.nlm.nih.gov/33476593/
- 368 Reck M, Rodríguez-Abreu D, Robinson A. et al. Updated Analysis of KEYNOTE-024: Pembrolizumab Versus Platinum-Based Chemotherapy for Advanced Non-Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score of 50% or Greater. J Clin Oncol 2019; 37: 537-546 https://pubmed.ncbi.nlm.nih.gov/30620668/
- 369 Reck M, Rodriguez-Abreu D, Robinson AG. et al. Pembrolizumab versus Chemotherapy for PD-L1-Positive Non-Small-Cell Lung Cancer. N Engl J Med 2016; 375: 1823-1833 https://www.ncbi.nlm.nih.gov/pubmed/27718847
- 370 Brahmer JR, Rodriguez-Abreu D, Robinson AG. et al. Health-related quality-of-life results for pembrolizumab versus chemotherapy in advanced, PD-L1-positive NSCLC (KEYNOTE-024): a multicentre, international, randomised, open-label phase 3 trial. Lancet Oncol 2017; 18: 1600-1609 https://www.ncbi.nlm.nih.gov/pubmed/29129441
- 371 Paz-Ares L, Luft A, Vicente D. et al. Pembrolizumab plus Chemotherapy for Squamous Non-Small-Cell Lung Cancer. N Engl J Med 2018; 379: 2040-2051 https://pubmed.ncbi.nlm.nih.gov/30280635/
- 372 Wu B, Lu S. The effect of PD-L1 categories-directed pembrolizumab plus chemotherapy for newly diagnosed metastatic non-small-cell lung cancer: a cost-effectiveness analysis. Transl Lung Cancer Res 2020; 9: 1770-1784 https://pubmed.ncbi.nlm.nih.gov/33209600/
- 373 de Castria TB, da Silva EM, Gois AF. et al. Cisplatin versus carboplatin in combination with third-generation drugs for advanced non-small cell lung cancer. Cochrane Database Syst Rev 2013; 8: CD009256 https://www.ncbi.nlm.nih.gov/pubmed/23949842
- 374 Rajeswaran A, Trojan A, Burnand B. et al. Efficacy and side effects of cisplatin- and carboplatin-based doublet chemotherapeutic regimens versus non-platinum-based doublet chemotherapeutic regimens as first line treatment of metastatic non-small cell lung carcinoma: a systematic review of randomized controlled trials. Lung Cancer 2008; 59: 1-11 https://www.ncbi.nlm.nih.gov/pubmed/17720276
- 375 Hotta K, Matsuo K, Ueoka H. et al. Meta-analysis of randomized clinical trials comparing Cisplatin to Carboplatin in patients with advanced non-small-cell lung cancer. J Clin Oncol 2004; 22: 3852-3859 https://www.ncbi.nlm.nih.gov/pubmed/15326195
- 376 Cartei G, Cartei F, Cantone A. et al. Cisplatin-cyclophosphamide-mitomycin combination chemotherapy with supportive care versus supportive care alone for treatment of metastatic non-small-cell lung cancer. J Natl Cancer Inst 1993; 85: 794-800 https://www.ncbi.nlm.nih.gov/pubmed/8387607
- 377 Ranson M, Davidson N, Nicolson M. et al. Randomized trial of paclitaxel plus supportive care versus supportive care for patients with advanced non-small-cell lung cancer. J Natl Cancer Inst 2000; 92: 1074-1080 https://www.ncbi.nlm.nih.gov/pubmed/10880550
- 378 D’Addario G, Pintilie M, Leighl NB. et al. Platinum-based versus non-platinum-based chemotherapy in advanced non-small-cell lung cancer: a meta-analysis of the published literature. J Clin Oncol 2005; 23: 2926-2936 https://www.ncbi.nlm.nih.gov/pubmed/15728229
- 379 Thongprasert S, Sanguanmitra P, Juthapan W. et al. Relationship between quality of life and clinical outcomes in advanced non-small cell lung cancer: best supportive care (BSC) versus BSC plus chemotherapy. Lung Cancer 1999; 24: 17-24 https://www.ncbi.nlm.nih.gov/pubmed/10403690
- 380 NSCLC Meta-Analyses Collaborative Group. Chemotherapy in addition to supportive care improves survival in advanced non-small-cell lung cancer: a systematic review and meta-analysis of individual patient data from 16 randomized controlled trials. J Clin Oncol 2008; 26: 4617-4625 https://www.ncbi.nlm.nih.gov/pubmed/18678835
- 381 Spiro SG, Rudd RM, Souhami RL. et al. Chemotherapy versus supportive care in advanced non-small cell lung cancer: improved survival without detriment to quality of life. Thorax 2004; 59: 828-836 https://www.ncbi.nlm.nih.gov/pubmed/15454647
- 382 Yuan S, Sun X, Li M. et al. A randomized study of involved-field irradiation versus elective nodal irradiation in combination with concurrent chemotherapy for inoperable stage III nonsmall cell lung cancer. Am J Clin Oncol 2007; 30: 239-244 https://www.ncbi.nlm.nih.gov/pubmed/17551299
- 383 Hellmann M, Paz-Ares L, Bernabe Caro R. et al. Nivolumab plus Ipilimumab in Advanced Non-Small-Cell Lung Cancer. N Engl J Med 2019; 381: 2020-2031 https://pubmed.ncbi.nlm.nih.gov/31562796/
- 384 Garon E, Hellmann M, Rizvi N. et al. Five-Year Overall Survival for Patients With Advanced Non-Small-Cell Lung Cancer Treated With Pembrolizumab: Results From the Phase I KEYNOTE-001 Study. J Clin Oncol 2019; 37: 2518-2527 https://pubmed.ncbi.nlm.nih.gov/31154919/
- 385 Mok T, Wu Y, Kudaba I. et al. Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042): a randomised, open-label, controlled, phase 3 trial. Lancet 2019; 393: 1819-1830 https://pubmed.ncbi.nlm.nih.gov/30955977/
- 386 Gadgeel S, Rodríguez-Abreu D, Speranza G. et al. Updated Analysis From KEYNOTE-189: Pembrolizumab or Placebo Plus Pemetrexed and Platinum for Previously Untreated Metastatic Nonsquamous Non-Small-Cell Lung Cancer. J Clin Oncol 2020; 38: 1505-1517
- 387 Gandhi L, Rodríguez-Abreu D, Gadgeel S. et al. Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer. N Engl J Med 2018; 378: 2078-2092
- 388 Nishio M, Barlesi F, West H. et al. Atezolizumab Plus Chemotherapy for First-Line Treatment of Nonsquamous NSCLC: Results From the Randomized Phase 3 IMpower132 Trial. J Thorac Oncol 2021; 16: 653-664
- 389 Reck M, Mok TSK, Nishio M. et al. Atezolizumab plus bevacizumab and chemotherapy in non-small-cell lung cancer (IMpower150): key subgroup analyses of patients with EGFR mutations or baseline liver metastases in a randomised, open-label phase 3 trial. The Lancet Respiratory Medicine 2019; 7: 387-401 https://doi.org/10.1016/S2213-2600(19)30084-0
- 390 Reck M, Schenker M, Lee KH. et al. Nivolumab plus ipilimumab versus chemotherapy as first-line treatment in advanced non-small-cell lung cancer with high tumour mutational burden: patient-reported outcomes results from the randomised, open-label, phase III CheckMate 227 trial. Eur J Cancer 2019; 116: 137-147
- 391 Gandhi L, Rodríguez-Abreu D, Gadgeel S. et al. Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer. N Engl J Med 2018; 378: 2078-2092 https://pubmed.ncbi.nlm.nih.gov/29658856/
- 392 Reck M, Mok TSK, Nishio M. et al. Atezolizumab plus bevacizumab and chemotherapy in non-small-cell lung cancer (IMpower150): key subgroup analyses of patients with EGFR mutations or baseline liver metastases in a randomised, open-label phase 3 trial. The Lancet Respiratory Medicine 2019; 7: 387-401 https://doi.org/10.1016/S2213-2600(19)30084-0
- 393 Pignon JP, Tribodet H, Scagliotti GV. et al. Lung Adjuvant Cisplatin Evaluation (LACE): A pooled analysis of five randomized clinical trials including 4,584 patients (2006 ASCO Annual Meeting Proceedings Part I). J Clin Oncol 2006; 24: 7008 https://ascopubs.org/doi/abs/10.1200/jco.2006.24.18_suppl.7008
- 394 Park JH, Lee CT, Lee HW. et al. Postoperative adjuvant chemotherapy for stage I non-small cell lung cancer. Eur J Cardiothorac Surg 2005; 27: 1086-1091 https://www.ncbi.nlm.nih.gov/pubmed/15896623
- 395 Strauss GM, Herndon JE, Maddaus MA. et al. Adjuvant chemotherapy in stage IB non-small cell lung cancer (NSCLC): Update of Cancer and Leukemia Group B protocol 9633. J Clin Oncol 2006; 24: 7007 https://ascopubs.org/doi/abs/10.1200/jco.2006.24.18_suppl.7007
- 396 Mineo TC, Ambrogi V, Corsaro V. et al. Postoperative adjuvant therapy for stage IB non-small-cell lung cancer. Eur J Cardiothorac Surg 2001; 20: 378-384 https://www.ncbi.nlm.nih.gov/pubmed/11463561
- 397 Alam N, Shepherd FA, Winton T. et al. Compliance with post-operative adjuvant chemotherapy in non-small cell lung cancer An analysis of National Cancer Institute of Canada and intergroup trial JBR10 and a review of the literature. Lung Cancer 2005; 47: 385-394 https://www.ncbi.nlm.nih.gov/pubmed/15713522
- 398 Endo C, Saito Y, Iwanami H. et al. A randomized trial of postoperative UFT therapy in p stage I, II non-small cell lung cancer: North-east Japan Study Group for Lung Cancer Surgery. Lung Cancer 2003; 40: 181-186 https://www.ncbi.nlm.nih.gov/pubmed/12711119
- 399 Kato H, Ichinose Y, Ohta M. et al. A randomized trial of adjuvant chemotherapy with uracil-tegafur for adenocarcinoma of the lung. N Engl J Med 2004; 350: 1713-1721 https://www.ncbi.nlm.nih.gov/pubmed/15102997
- 400 Nakagawa M, Tanaka F, Tsubota N. et al. A randomized phase III trial of adjuvant chemotherapy with UFT for completely resected pathological stage I non-small-cell lung cancer: the West Japan Study Group for Lung Cancer Surgery (WJSG) – the 4th study. Ann Oncol 2005; 16: 75-80 https://www.ncbi.nlm.nih.gov/pubmed/15598942
- 401 Hamada C, Tanaka F, Ohta M. et al. Meta-analysis of postoperative adjuvant chemotherapy with tegafur-uracil in non-small-cell lung cancer. J Clin Oncol 2005; 23: 4999-5006 https://www.ncbi.nlm.nih.gov/pubmed/16051951
- 402 Wada H, Miyahara R, Tanaka F. et al. Postoperative adjuvant chemotherapy with PVM (Cisplatin + Vindesine + Mitomycin C) and UFT (Uracil + Tegaful) in resected stage I-II NSCLC (non-small cell lung cancer): a randomized clinical trial West Japan Study Group for lung cancer surgery (WJSG). Eur J Cardiothorac Surg 1999; 15: 438-443 https://www.ncbi.nlm.nih.gov/pubmed/10371118
- 403 Rowell NP, Williams CJ. Radical radiotherapy for stage I/II non-small cell lung cancer in patients not sufficiently fit for or declining surgery (medically inoperable). Cochrane Database Syst Rev 2001; CD002935 https://www.ncbi.nlm.nih.gov/pubmed/11406051
- 404 Jeremic B, Shibamoto Y, Acimovic L. et al. A randomized trial of three single-dose radiation therapy regimens in the treatment of metastatic bone pain. Int J Radiat Oncol Biol Phys 1998; 42: 161-167 https://www.ncbi.nlm.nih.gov/pubmed/9747834
- 405 Fidias PM, Dakhil SR, Lyss AP. et al. Phase III study of immediate compared with delayed docetaxel after front-line therapy with gemcitabine plus carboplatin in advanced non-small-cell lung cancer. J Clin Oncol 2009; 27: 591-598 https://www.ncbi.nlm.nih.gov/pubmed/19075278
- 406 Gridelli C, Ardizzoni A, Le Chevalier T. et al. Treatment of advanced non-small-cell lung cancer patients with ECOG performance status 2: results of an European Experts Panel. Ann Oncol 2004; 15: 419-426 https://www.ncbi.nlm.nih.gov/pubmed/14998843
- 407 Pujol JL, Paz-Ares L, de Marinis F. et al. Long-term and low-grade safety results of a phase III study (PARAMOUNT): maintenance pemetrexed plus best supportive care versus placebo plus best supportive care immediately after induction treatment with pemetrexed plus cisplatin for advanced nonsquamous non-small-cell lung cancer. Clin Lung Cancer 2014; 15: 418-425 https://www.ncbi.nlm.nih.gov/pubmed/25104617
- 408 Reck M, Paz-Ares LG, de Marinis F. et al. PARAMOUNT: Descriptive subgroup analyses of final overall survival for the phase III study of maintenance pemetrexed versus placebo following induction treatment with pemetrexed plus cisplatin for advanced nonsquamous non-small-cell lung cancer. J Thorac Oncol 2014; 9: 205-213 https://www.ncbi.nlm.nih.gov/pubmed/24419418
- 409 Paz-Ares LG, de Marinis F, Dediu M. et al. PARAMOUNT: Final overall survival results of the phase III study of maintenance pemetrexed versus placebo immediately after induction treatment with pemetrexed plus cisplatin for advanced nonsquamous non-small-cell lung cancer. J Clin Oncol 2013; 31: 2895-2902 https://www.ncbi.nlm.nih.gov/pubmed/23835707
- 410 Belani CP, Barstis J, Perry MC. et al. Multicenter, randomized trial for stage IIIB or IV non-small-cell lung cancer using weekly paclitaxel and carboplatin followed by maintenance weekly paclitaxel or observation. J Clin Oncol 2003; 21: 2933-2939 https://www.ncbi.nlm.nih.gov/pubmed/12885812
- 411 Westeel V, Quoix E, Moro-Sibilot D. et al. Randomized study of maintenance vinorelbine in responders with advanced non-small-cell lung cancer. J Natl Cancer Inst 2005; 97: 499-506 https://www.ncbi.nlm.nih.gov/pubmed/15812075
- 412 Brodowicz T, Krzakowski M, Zwitter M. et al. Cisplatin and gemcitabine first-line chemotherapy followed by maintenance gemcitabine or best supportive care in advanced non-small cell lung cancer: a phase III trial. Lung Cancer 2006; 52: 155-163 https://www.ncbi.nlm.nih.gov/pubmed/16569462
- 413 Socinski MA, Schell MJ, Peterman A. et al. Phase III trial comparing a defined duration of therapy versus continuous therapy followed by second-line therapy in advanced-stage IIIB/IV non-small-cell lung cancer. J Clin Oncol 2002; 20: 1335-1343 https://www.ncbi.nlm.nih.gov/pubmed/11870177
- 414 Smith IE, O’Brien ME, Talbot DC. et al. Duration of chemotherapy in advanced non-small-cell lung cancer: a randomized trial of three versus six courses of mitomycin, vinblastine, and cisplatin. J Clin Oncol 2001; 19: 1336-1343 https://www.ncbi.nlm.nih.gov/pubmed/11230476
- 415 Borget I, Perol M, Perol D. et al. Cost-utility analysis of maintenance therapy with gemcitabine or erlotinib vs observation with predefined second-line treatment after cisplatin-gemcitabine induction chemotherapy for advanced NSCLC: IFCT-GFPC 0502-Eco phase III study. BMC Cancer 2014; 14: 953 https://www.ncbi.nlm.nih.gov/pubmed/25511923
- 416 Bylicki O, Ferlay C, Chouaid C. et al. Efficacy of pemetrexed as second-line therapy in advanced NSCLC after either treatment-free interval or maintenance therapy with gemcitabine or erlotinib in IFCT-GFPC 05-02 phase III study. J Thorac Oncol 2013; 8: 906-914 https://www.ncbi.nlm.nih.gov/pubmed/23591160
- 417 Tsao MS, Sakurada A, Cutz JC. et al. Erlotinib in lung cancer – molecular and clinical predictors of outcome. N Engl J Med 2005; 353: 133-144 https://www.ncbi.nlm.nih.gov/pubmed/16014883
- 418 Shepherd FA, Dancey J, Ramlau R. et al. Prospective randomized trial of docetaxel versus best supportive care in patients with non-small-cell lung cancer previously treated with platinum-based chemotherapy. J Clin Oncol 2000; 18: 2095-2103 https://www.ncbi.nlm.nih.gov/pubmed/10811675
- 419 Fossella FV, DeVore R, Kerr RN. et al. Randomized phase III trial of docetaxel versus vinorelbine or ifosfamide in patients with advanced non-small-cell lung cancer previously treated with platinum-containing chemotherapy regimens The TAX 320 Non-Small Cell Lung Cancer Study Group. J Clin Oncol 2000; 18: 2354-2362 https://www.ncbi.nlm.nih.gov/pubmed/10856094
- 420 Hanna N, Shepherd FA, Fossella FV. et al. Randomized phase III trial of pemetrexed versus docetaxel in patients with non-small-cell lung cancer previously treated with chemotherapy. J Clin Oncol 2004; 22: 1589-1597 https://www.ncbi.nlm.nih.gov/pubmed/15117980
- 421 Soria JC, Felip E, Cobo M. et al. Afatinib versus erlotinib as second-line treatment of patients with advanced squamous cell carcinoma of the lung (LUX-Lung 8): an open-label randomised controlled phase 3 trial. Lancet Oncol 2015; 16: 897-907 https://www.ncbi.nlm.nih.gov/pubmed/26156651
- 422 Brahmer J, Reckamp KL, Baas P. et al. Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer. N Engl J Med 2015; 373: 123-135 https://www.ncbi.nlm.nih.gov/pubmed/26028407
- 423 Garon EB, Ciuleanu TE, Arrieta O. et al. Ramucirumab plus docetaxel versus placebo plus docetaxel for second-line treatment of stage IV non-small-cell lung cancer after disease progression on platinum-based therapy (REVEL): a multicentre, double-blind, randomised phase 3 trial. Lancet 2014; 384: 665-673 https://www.ncbi.nlm.nih.gov/pubmed/24933332
- 424 Herbst RS, Baas P, Kim DW. et al. Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial. Lancet 2016; 387: 1540-1550 https://www.ncbi.nlm.nih.gov/pubmed/26712084
- 425 Greenhalgh J, Boland A, Bates V. et al. First-line treatment of advanced epidermal growth factor receptor (EGFR) mutation positive non-squamous non-small cell lung cancer. Cochrane Database Syst Rev 2021; 3: Cd010383
- 426 Mok T, Wu YL, Thongprasert S. et al. Gefitinib or Carboplatin-Paclitaxel in pulmonary adenocarcinoma. N Engl J Med 2009; 361: 947-957 https://www.ncbi.nlm.nih.gov/pubmed/19692680
- 427 Rosell R, Moran T, Queralt C. et al. Screening for epidermal growth factor receptor mutations in lung cancer. N Engl J Med 2009; 361: 958-967 https://www.ncbi.nlm.nih.gov/pubmed/19692684
- 428 Fukuoka M, Wu YL, Thongprasert S. et al. Biomarker analyses and final overall survival results from a phase III, randomized, open-label, first-line study of gefitinib versus carboplatin/paclitaxel in clinically selected patients with advanced non-small-cell lung cancer in Asia (IPASS). J Clin Oncol 2011; 29: 2866-2874 https://www.ncbi.nlm.nih.gov/pubmed/21670455
- 429 Han JY, Park K, Kim SW. et al. First-SIGNAL: first-line single-agent iressa versus gemcitabine and cisplatin trial in never-smokers with adenocarcinoma of the lung. J Clin Oncol 2012; 30: 1122-1128 https://www.ncbi.nlm.nih.gov/pubmed/22370314
- 430 Mitsudomi T, Morita S, Yatabe Y. et al. Gefitinib versus cisplatin plus docetaxel in patients with non-small-cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomised phase 3 trial. Lancet Oncol 2010; 11: 121-128
- 431 Maemondo M, Inoue A, Kobayashi K. et al. Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR. N Engl J Med 2010; 362: 2380-2388 https://www.ncbi.nlm.nih.gov/pubmed/20573926
- 432 Sequist LV, Yang JC, Yamamoto N. et al. Phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations. J Clin Oncol 2013; 31: 3327-3334 https://www.ncbi.nlm.nih.gov/pubmed/23816960
- 433 Yang JC, Hirsh V, Schuler M. et al. Symptom control and quality of life in LUX-Lung 3: a phase III study of afatinib or cisplatin/pemetrexed in patients with advanced lung adenocarcinoma with EGFR mutations. J Clin Oncol 2013; 31: 3342-3350 https://www.ncbi.nlm.nih.gov/pubmed/23816967
- 434 Yang JC, Wu YL, Schuler M. et al. Afatinib versus cisplatin-based chemotherapy for EGFR mutation-positive lung adenocarcinoma (LUX-Lung 3 and LUX-Lung 6): analysis of overall survival data from two randomised, phase 3 trials. Lancet Oncol 2015; 16: 141-151 https://www.ncbi.nlm.nih.gov/pubmed/25589191
- 435 Zhou C, Wu YL, Chen G. et al. Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study. Lancet Oncol 2011; 12: 735-742 https://www.ncbi.nlm.nih.gov/pubmed/21783417
- 436 Yang JC, Sequist LV, Geater SL. et al. Clinical activity of afatinib in patients with advanced non-small-cell lung cancer harbouring uncommon EGFR mutations: a combined post-hoc analysis of LUX-Lung 2, LUX-Lung 3, and LUX-Lung 6. Lancet Oncol 2015; 16: 830-838 https://www.ncbi.nlm.nih.gov/pubmed/26051236
- 437 Park K, Tan EH, O‘Byrne K. et al. Afatinib versus gefitinib as first-line treatment of patients with EGFR mutation-positive non-small-cell lung cancer (LUX-Lung 7): a phase 2B, open-label, randomised controlled trial. Lancet Oncol 2016; 17: 577-589 https://www.ncbi.nlm.nih.gov/pubmed/27083334
- 438 Ramalingam SS, Vansteenkiste J, Planchard D. et al. Overall Survival with Osimertinib in Untreated, EGFR-Mutated Advanced NSCLC. N Engl J Med 2020; 382: 41-50
- 439 Cho J, Lim S, An H. et al. Osimertinib for Patients With Non-Small-Cell Lung Cancer Harboring Uncommon EGFR Mutations: A Multicenter, Open-Label, Phase II Trial (KCSG-LU15-09). J Clin Oncol 2020; 38: 488-495 https://pubmed.ncbi.nlm.nih.gov/31825714/
- 440 Kobayashi Y, Mitsudomi T. Not all epidermal growth factor receptor mutations in lung cancer are created equal: Perspectives for individualized treatment strategy. Cancer Sci 2016; 107: 1179-1186 https://pubmed.ncbi.nlm.nih.gov/27323238/
- 441 Mok TS, Wu Y, Ahn M. et al. Osimertinib or Platinum-Pemetrexed in EGFR T790M-Positive Lung Cancer. New England Journal of Medicine 2017; 376: 629-640
- 442 Park K, Haura E, Leighl N. et al. Amivantamab in EGFR Exon 20 Insertion-Mutated Non-Small-Cell Lung Cancer Progressing on Platinum Chemotherapy: Initial Results From the CHRYSALIS Phase I Study. J Clin Oncol 2021; 39: 3391-3402 https://pubmed.ncbi.nlm.nih.gov/34339292/
- 443 Janne PA, Yang JC, Kim DW. et al. AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer. N Engl J Med 2015; 372: 1689-1699 https://www.ncbi.nlm.nih.gov/pubmed/25923549
- 444 Mok TS, Wu Y, Ahn M. et al. Osimertinib or Platinum-Pemetrexed in EGFR T790M-Positive Lung Cancer. New England Journal of Medicine 2017; 376: 629-640
- 445 Camidge D, Kim H, Ahn M. et al. Brigatinib Versus Crizotinib in ALK Inhibitor-Naive Advanced ALK-Positive NSCLC: Final Results of Phase 3 ALTA-1L Trial. J Thorac Oncol 2021; 16: 2091-2108 https://pubmed.ncbi.nlm.nih.gov/34537440/
- 446 Camidge D, Kim H, Ahn M. et al. Brigatinib Versus Crizotinib in Advanced ALK Inhibitor-Naive ALK-Positive Non-Small Cell Lung Cancer: Second Interim Analysis of the Phase III ALTA-1L Trial. J Clin Oncol 2020; 38: 3592-3603 https://pubmed.ncbi.nlm.nih.gov/32780660/
- 447 Camidge D, Kim H, Ahn M. et al. Brigatinib versus Crizotinib in ALK-Positive Non-Small-Cell Lung Cancer. N Engl J Med 2018; 379: 2027-2039 https://pubmed.ncbi.nlm.nih.gov/30280657/
- 448 Gettinger S, Huber R, Kim D. et al. Long-Term Efficacy and Safety of Brigatinib in Crizotinib-Refractory. JTO Clin Res Rep 2022; 3: 100385 https://pubmed.ncbi.nlm.nih.gov/36065449/
- 449 Ignatius Ou S-H, Nishio M, Ahn M. et al. Efficacy of Brigatinib in Patients With Advanced Anaplastic Lymphoma Kinase-Positive Non-Small Cell Lung Cancer Who Progressed on Alectinib or Ceritinib: ALTA-2 Study. J Thorac Oncol 2022; 17: 1404-1414 https://pubmed.ncbi.nlm.nih.gov/36096442/
- 450 Shaw A, Bauer T, de Marinis F. et al. First-Line Lorlatinib or Crizotinib in Advanced. N Engl J Med 2020; 383: 2018-2029 https://pubmed.ncbi.nlm.nih.gov/33207094/
- 451 Kron A, Alidousty C, Scheffler M. et al. Impact of TP53 mutation status on systemic treatment outcome in ALK-rearranged non-small-cell lung cancer. Ann Oncol 2018; 29: 2068-2075 https://pubmed.ncbi.nlm.nih.gov/30165392/
- 452 Mok T, Camidge D, Gadgeel S. et al. Updated overall survival and final progression-free survival data for patients with treatment-naive advanced ALK-positive non-small-cell lung cancer in the ALEX study. Ann Oncol 2020; 31: 1056-1064 https://pubmed.ncbi.nlm.nih.gov/32418886/
- 453 Solomon BJ, Mok T, Kim DW. et al. First-line crizotinib versus chemotherapy in ALK-positive lung cancer. N Engl J Med 2014; 371: 2167-2177 https://www.ncbi.nlm.nih.gov/pubmed/25470694
- 454 Soria J, Tan DSW, Chiari R. et al. First-line ceritinib versus platinum-based chemotherapy in advanced ALK-rearranged non-small-cell lung cancer (ASCEND-4): a randomised, open-label, phase 3 study. The Lancet 2017; 389: 917-929 https://www.thelancet.com/pdfs/journals/lancet/PIIS0140-6736(17)30123-X.pdf
- 455 Cho BC, Kim DW, Bearz A. et al. ASCEND-8: A Randomized Phase 1 Study of Ceritinib, 450 mg or 600 mg, Taken with a Low-Fat Meal versus 750 mg in Fasted State in Patients with Anaplastic Lymphoma Kinase (ALK)-Rearranged Metastatic Non-Small Cell Lung Cancer (NSCLC). J Thorac Oncol 2017; 12: 1357-1367 https://www.ncbi.nlm.nih.gov/pubmed/28729021
- 456 Peters S, Camidge DR, Shaw AT. et al. Alectinib versus Crizotinib in Untreated ALK-Positive Non-Small-Cell Lung Cancer. New England Journal of Medicine 2017; 377: 829-838 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296421/
- 457 Camidge D, Kim H, Ahn M. et al. Brigatinib Versus Crizotinib in Advanced ALK Inhibitor-Naive ALK-Positive Non-Small Cell Lung Cancer: Second Interim Analysis of the Phase III ALTA-1L Trial. J Clin Oncol 2020; 38: 3592-3603 https://pubmed.ncbi.nlm.nih.gov/32780660/
- 458 A genomics-based classification of human lung tumors. Sci Transl Med 2013; 5: 209ra153 https://www.ncbi.nlm.nih.gov/pubmed/24174329
- 459 Shaw AT, Kim DW, Nakagawa K. et al. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N Engl J Med 2013; 368: 2385-2394 https://www.ncbi.nlm.nih.gov/pubmed/23724913
- 460 Shaw AT, Kim DW, Mehra R. et al. Ceritinib in ALK-rearranged non-small-cell lung cancer. N Engl J Med 2014; 370: 1189-1197 https://www.ncbi.nlm.nih.gov/pubmed/24670165
- 461 Shaw AT, Solomon BJ, Besse B. et al. ALK Resistance Mutations and Efficacy of Lorlatinib in Advanced Anaplastic Lymphoma Kinase-Positive Non-Small-Cell Lung Cancer. J Clin Oncol 2019; 37: 1370-1379
- 462 Wu Y, Yang J, Kim D. et al. Phase II Study of Crizotinib in East Asian Patients With ROS1-Positive Advanced Non-Small-Cell Lung Cancer. J Clin Oncol 2018; 36: 1405-1411 https://pubmed.ncbi.nlm.nih.gov/29596029/
- 463 Michels S, Massutí B, Schildhaus H. et al. Safety and Efficacy of Crizotinib in Patients With Advanced or Metastatic ROS1-Rearranged Lung Cancer (EUCROSS): A European Phase II Clinical Trial. J Thorac Oncol 2019; 14: 1266-1276 https://pubmed.ncbi.nlm.nih.gov/30978502/
- 464 Landi L, Chiari R, Tiseo M. et al. Crizotinib in. Clin Cancer Res 2019; 25: 7312-7319 https://pubmed.ncbi.nlm.nih.gov/31416808/
- 465 Drilon A, Siena S, Dziadziuszko R. et al. Entrectinib in ROS1 fusion-positive non-small-cell lung cancer: integrated analysis of three phase 1-2 trials. Lancet Oncol 2020; 21: 261-270 https://pubmed.ncbi.nlm.nih.gov/31838015/
- 466 Shaw AT, Ou SH, Bang YJ. et al. Crizotinib in ROS1-rearranged non-small-cell lung cancer. N Engl J Med 2014; 371: 1963-1971 https://www.ncbi.nlm.nih.gov/pubmed/25264305
- 467 Mazieres J, Zalcman G, Crino L. et al. Crizotinib therapy for advanced lung adenocarcinoma and a ROS1 rearrangement: results from the EUROS1 cohort. J Clin Oncol 2015; 33: 992-999 https://www.ncbi.nlm.nih.gov/pubmed/25667280
- 468 Planchard D, Smit E, Groen H. et al. Dabrafenib plus trametinib in patients with previously untreated BRAF. Lancet Oncol 2017; 18: 1307-1316 https://pubmed.ncbi.nlm.nih.gov/28919011/
- 469 Gautschi O, Milia J, Cabarrou B. et al. Targeted Therapy for Patients with BRAF-Mutant Lung Cancer: Results from the European EURAF Cohort. J Thorac Oncol 2015; 10: 1451-1457 https://pubmed.ncbi.nlm.nih.gov/26200454/
- 470 Hyman D, Puzanov I, Subbiah V. et al. Vemurafenib in Multiple Nonmelanoma Cancers with BRAF V600 Mutations. N Engl J Med 2015; 373: 726-736 https://pubmed.ncbi.nlm.nih.gov/26287849/
- 471 Griesinger F, Curigliano G, Thomas M. et al. Safety and efficacy of pralsetinib in RET fusion-positive non-small-cell lung cancer including as first-line therapy: update from the ARROW trial. Ann Oncol 2022; 33: 1168-1178 https://pubmed.ncbi.nlm.nih.gov/35973665/
- 472 Gainor J, Curigliano G, Kim D. et al. Pralsetinib for RET fusion-positive non-small-cell lung cancer (ARROW): a multi-cohort, open-label, phase ½ study. Lancet Oncol 2021; 22: 959-969 https://pubmed.ncbi.nlm.nih.gov/34118197/
- 473 Paik P, Felip E, Veillon R. et al. Tepotinib in Non-Small-Cell Lung Cancer with. N Engl J Med 2020; 383: 931-943 https://pubmed.ncbi.nlm.nih.gov/32469185/
- 474 Wolf J, Seto T, Han JY. et al. Capmatinib in MET Exon 14-Mutated or MET-Amplified Non-Small-Cell Lung Cancer. N Engl J Med 2020; 383: 944-957 https://www.nejm.org/doi/full/10.1056/NEJMoa2002787
- 475 Skoulidis F, Li B, Dy G. et al. Sotorasib for Lung Cancers with. N Engl J Med 2021; 384: 2371-2381 https://pubmed.ncbi.nlm.nih.gov/34096690/
- 476 De Ruysscher D, Wanders R, Hendriks L. et al. Progression-Free Survival and Overall Survival Beyond 5 Years of NSCLC Patients With Synchronous Oligometastases Treated in a Prospective Phase II Trial (NCT 01282450). J Thorac Oncol 2018; 13: 1958-1961 https://pubmed.ncbi.nlm.nih.gov/30253974/
- 477 Gomez D, Blumenschein G, Lee J. et al. Local consolidative therapy versus maintenance therapy or observation for patients with oligometastatic non-small-cell lung cancer without progression after first-line systemic therapy: a multicentre, randomised, controlled, phase 2 study. Lancet Oncol 2016; 17: 1672-1682 https://pubmed.ncbi.nlm.nih.gov/27789196/
- 478 Iyengar P, Wardak Z, Gerber D. et al. Consolidative Radiotherapy for Limited Metastatic Non-Small-Cell Lung Cancer: A Phase 2 Randomized Clinical Trial. JAMA Oncol 2018; 4: e173501 https://pubmed.ncbi.nlm.nih.gov/28973074/
- 479 Collen C, Christian N, Schallier D. et al. Phase II study of stereotactic body radiotherapy to primary tumor and metastatic locations in oligometastatic nonsmall-cell lung cancer patients. Ann Oncol 2014; 25: 1954-1959 https://www.ncbi.nlm.nih.gov/pubmed/25114022
- 480 Petty W, Urbanic J, Ahmed T. et al. Long-Term Outcomes of a Phase 2 Trial of Chemotherapy With Consolidative Radiation Therapy for Oligometastatic Non-Small Cell Lung Cancer. Int J Radiat Oncol Biol Phys 2018; 102: 527-535 https://pubmed.ncbi.nlm.nih.gov/30003996/
- 481 Arrieta O, Barrón F, Maldonado F. et al. Radical consolidative treatment provides a clinical benefit and long-term survival in patients with synchronous oligometastatic non-small cell lung cancer: A phase II study. Lung Cancer 2019; 130: 67-75 https://pubmed.ncbi.nlm.nih.gov/30885354/
- 482 Bauml J, Mick R, Ciunci C. et al. Pembrolizumab After Completion of Locally Ablative Therapy for Oligometastatic Non-Small Cell Lung Cancer: A Phase 2 Trial. JAMA Oncol 2019; 5: 1283-1290 https://pubmed.ncbi.nlm.nih.gov/31294762/
- 483 Gomez D, Tang C, Zhang J. et al. Local Consolidative Therapy Vs Maintenance Therapy or Observation for Patients With Oligometastatic Non-Small-Cell Lung Cancer: Long-Term Results of a Multi-Institutional, Phase II, Randomized Study. J Clin Oncol 2019; 37: 1558-1565 https://pubmed.ncbi.nlm.nih.gov/31067138/
- 484 Palma D, Olson R, Harrow S. et al. Stereotactic ablative radiotherapy versus standard of care palliative treatment in patients with oligometastatic cancers (SABR-COMET): a randomised, phase 2, open-label trial. Lancet 2019; 393: 2051-2058 https://pubmed.ncbi.nlm.nih.gov/30982687/
- 485 Wang X, Bai Y, Verma V. et al. Randomized Trial of First-Line Tyrosine Kinase Inhibitor With or Without Radiotherapy for Synchronous Oligometastatic EGFR-Mutated NSCLC. J Natl Cancer Inst 2023; 115: 742-748 https://pubmed.ncbi.nlm.nih.gov/35094066/
- 486 Govindan R, Page N, Morgensztern D. et al. Changing epidemiology of small-cell lung cancer in the United States over the last 30 years: analysis of the surveillance, epidemiologic, and end results database. J Clin Oncol 2006; 24: 4539-4544 https://www.ncbi.nlm.nih.gov/pubmed/17008692
- 487 Lüchtenborg M, Riaz S, Lim E. et al. Survival of patients with small cell lung cancer undergoing lung resection in England, 1998–2009. Thorax 2014; 69: 269-273 https://pubmed.ncbi.nlm.nih.gov/24172710/
- 488 Liu T, Chen Z, Dang J. et al. The role of surgery in stage I to III small cell lung cancer: A systematic review and meta-analysis. PLoS One 2018; 13: e0210001 https://pubmed.ncbi.nlm.nih.gov/30596754/
- 489 Albain KS, Crowley JJ, LeBlanc M. et al. Determinants of improved outcome in small-cell lung cancer: an analysis of the 2,580-patient Southwest Oncology Group data base. J Clin Oncol 1990; 8: 1563-1574 https://www.ncbi.nlm.nih.gov/pubmed/2167954
- 490 Rawson NS, Peto J. An overview of prognostic factors in small cell lung cancer A report from the Subcommittee for the Management of Lung Cancer of the United Kingdom Coordinating Committee on Cancer Research. Br J Cancer 1990; 61: 597-604 https://www.ncbi.nlm.nih.gov/pubmed/2158808
- 491 Bremnes RM, Sundstrom S, Aasebo U. et al. The value of prognostic factors in small cell lung cancer: results from a randomised multicenter study with minimum 5 year follow-up. Lung Cancer 2003; 39: 303-313 https://www.ncbi.nlm.nih.gov/pubmed/12609569
- 492 Cerny T, Blair V, Anderson H. et al. Pretreatment prognostic factors and scoring system in 407 small-cell lung cancer patients. Int J Cancer 1987; 39: 146-149 https://www.ncbi.nlm.nih.gov/pubmed/3026969
- 493 Spiegelman D, Maurer LH, Ware JH. et al. Prognostic factors in small-cell carcinoma of the lung: an analysis of 1,521 patients. J Clin Oncol 1989; 7: 344-354 https://www.ncbi.nlm.nih.gov/pubmed/2537384
- 494 Sagman U, Maki E, Evans WK. et al. Small-cell carcinoma of the lung: derivation of a prognostic staging system. J Clin Oncol 1991; 9: 1639-1649 https://www.ncbi.nlm.nih.gov/pubmed/1651996
- 495 Wolf M, Holle R, Hans K. et al. Analysis of prognostic factors in 766 patients with small cell lung cancer (SCLC): the role of sex as a predictor for survival. Br J Cancer 1991; 63: 986-992 https://www.ncbi.nlm.nih.gov/pubmed/1648949
- 496 Singh S, Parulekar W, Murray N. et al. Influence of sex on toxicity and treatment outcome in small-cell lung cancer. J Clin Oncol 2005; 23: 850-856 https://www.ncbi.nlm.nih.gov/pubmed/15681530
- 497 Ludbrook JJ, Truong PT, MacNeil MV. et al. Do age and comorbidity impact treatment allocation and outcomes in limited stage small-cell lung cancer? A community-based population analysis. Int J Radiat Oncol Biol Phys 2003; 55: 1321-1330 https://www.ncbi.nlm.nih.gov/pubmed/12654444
- 498 Johnson PW, Joel SP, Love S. et al. Tumour markers for prediction of survival and monitoring of remission in small cell lung cancer. Br J Cancer 1993; 67: 760-766
- 499 Wakeam E, Acuna S, Leighl N. et al. Surgery Versus Chemotherapy and Radiotherapy For Early and Locally Advanced Small Cell Lung Cancer: A Propensity-Matched Analysis of Survival. Lung Cancer 2017; 109: 78-88 https://pubmed.ncbi.nlm.nih.gov/28577955/
- 500 Combs S, Hancock J, Boffa D. et al. Bolstering the case for lobectomy in stages I, II, and IIIA small-cell lung cancer using the National Cancer Data Base. J Thorac Oncol 2015; 10: 316-323 https://pubmed.ncbi.nlm.nih.gov/25319182/
- 501 Schreiber D, Rineer J, Weedon J. et al. Survival outcomes with the use of surgery in limited-stage small cell lung cancer: should its role be re-evaluated?. Cancer 2010; 116: 1350-1357 https://pubmed.ncbi.nlm.nih.gov/20082453/
- 502 Liu Y, Shan L, Shen J. et al. Choice of surgical procedure – lobectomy, segmentectomy, or wedge resection – for patients with stage T1-2N0M0 small cell lung cancer: A population-based study. Thorac Cancer 2019; 10: 593-600 https://pubmed.ncbi.nlm.nih.gov/30854808/
- 503 Li Y, Hu S, Xie J. et al. Effects of surgery on survival of elderly patients with stage I small-cell lung cancer: analysis of the SEER database. J Cancer Res Clin Oncol 2019; 145: 2397-2404 https://pubmed.ncbi.nlm.nih.gov/31302755/
- 504 Xu J, Yang H, Fu X. et al. Prophylactic Cranial Irradiation for Patients with Surgically Resected Small Cell Lung Cancer. J Thorac Oncol 2017; 12: 347-353 https://pubmed.ncbi.nlm.nih.gov/27725211/
- 505 Yang C, Chan D, Shah S. et al. Long-term Survival After Surgery Compared With Concurrent Chemoradiation for Node-negative Small Cell Lung Cancer. Ann Surg 2018; 268: 1105-1112 https://pubmed.ncbi.nlm.nih.gov/28475559/
- 506 Babakoohi S, Fu P, Yang M. et al. Combined SCLC clinical and pathologic characteristics. Clin Lung Cancer 2013; 14: 113-119 https://pubmed.ncbi.nlm.nih.gov/23010092/
- 507 Ulsperger E, Karrer K, Denck H. Multimodality treatment for small cell bronchial carcinoma Preliminary results of a prospective, multicenter trial The ISC-Lung Cancer Study Group. Eur J Cardiothorac Surg 1991; 5: 306-309 https://www.ncbi.nlm.nih.gov/pubmed/1651741
- 508 Shepherd FA, Ginsberg RJ, Feld R. et al. Surgical treatment for limited small-cell lung cancer. J Thorac Cardiovasc Surg 1991; 101: 385-393 https://www.ncbi.nlm.nih.gov/pubmed/1847981
- 509 Tsuchiya R, Suzuki K, Ichinose Y. et al. Phase II trial of postoperative adjuvant cisplatin and etoposide in patients with completely resected stage I-IIIa small cell lung cancer: the Japan Clinical Oncology Lung Cancer Study Group Trial (JCOG9101). J Thorac Cardiovasc Surg 2005; 129: 977-983 https://www.ncbi.nlm.nih.gov/pubmed/15867769
- 510 Fox W, Scadding JG. Medical Research Council comparative trial of surgery and radiotherapy for primary treatment of small-celled or oat-celled carcinoma of bronchus Ten-year follow-up. Lancet 1973; 2: 63-65 https://www.ncbi.nlm.nih.gov/pubmed/4123619
- 511 Maassen W, Greschuchna D, Martinez I. The role of surgery in the treatment of small cell carcinoma of the lung. Recent Results Cancer Res 1985; 97: 107-115 https://www.ncbi.nlm.nih.gov/pubmed/2986238
- 512 Osterlind K, Hansen M, Hansen HH. et al. Treatment policy of surgery in small cell carcinoma of the lung: retrospective analysis of a series of 874 consecutive patients. Thorax 1985; 40: 272-277 https://www.ncbi.nlm.nih.gov/pubmed/2992111
- 513 Salem A, Mistry H, Hatton M. et al. Association of Chemoradiotherapy With Outcomes Among Patients With Stage I to II vs Stage III Small Cell Lung Cancer: Secondary Analysis of a Randomized Clinical Trial. JAMA Oncol 2019; 5: e185335 https://pubmed.ncbi.nlm.nih.gov/30520977/
- 514 Kim E, Biswas T, Bakaki P. et al. Comparison of cisplatin/etoposide versus carboplatin/etoposide concurrent chemoradiation therapy for limited-stage small cell lung cancer (LS-SCLC) in the elderly population (age >65 years) using national SEER-Medicare data. Pract Radiat Oncol 2016; 6: e163-e169 https://pubmed.ncbi.nlm.nih.gov/27142494/
- 515 Mascaux C, Paesmans M, Berghmans T. et al. A systematic review of the role of etoposide and cisplatin in the chemotherapy of small cell lung cancer with methodology assessment and meta-analysis. Lung Cancer 2000; 30: 23-36 https://www.ncbi.nlm.nih.gov/pubmed/11008007
- 516 Pujol JL, Carestia L, Daures JP. Is there a case for cisplatin in the treatment of small-cell lung cancer? A meta-analysis of randomized trials of a cisplatin-containing regimen versus a regimen without this alkylating agent. Br J Cancer 2000; 83: 8-15 https://www.ncbi.nlm.nih.gov/pubmed/10883661
- 517 Maksymiuk AW, Jett JR, Earle JD. et al. Sequencing and schedule effects of cisplatin plus etoposide in small-cell lung cancer: results of a North Central Cancer Treatment Group randomized clinical trial. J Clin Oncol 1994; 12: 70-76 https://www.ncbi.nlm.nih.gov/pubmed/8270988
- 518 Sundstrom S, Bremnes RM, Kaasa S. et al. Cisplatin and etoposide regimen is superior to cyclophosphamide, epirubicin, and vincristine regimen in small cell lung cancer: results from a randomized phase III trial with 5 years’ follow-up. J Clin Oncol 2002; 20: 4665-4672 https://www.ncbi.nlm.nih.gov/pubmed/12488411
- 519 Thatcher N, Qian W, Clark PI. et al. Ifosfamide, carboplatin, and etoposide with midcycle vincristine versus standard chemotherapy in patients with small-cell lung cancer and good performance status: clinical and quality-of-life results of the British Medical Research Council multicenter randomized LU21 trial. J Clin Oncol 2005; 23: 8371-8379 https://www.ncbi.nlm.nih.gov/pubmed/16293867
- 520 Einhorn LH, Crawford J, Birch R. et al. Cisplatin plus etoposide consolidation following cyclophosphamide, doxorubicin, and vincristine in limited small-cell lung cancer. J Clin Oncol 1988; 6: 451-456 https://www.ncbi.nlm.nih.gov/pubmed/2832549
- 521 Wolf M, Havemann K, Holle R. et al. Cisplatin/etoposide versus ifosfamide/etoposide combination chemotherapy in small-cell lung cancer: a multicenter German randomized trial. J Clin Oncol 1987; 5: 1880-1889 https://www.ncbi.nlm.nih.gov/pubmed/2824710
- 522 Jackson DV, Zekan PJ, Caldwell RD. et al. VP-16-213 in combination chemotherapy with chest irradiation for small-cell lung cancer: a randomized trial of the Piedmont Oncology Association. J Clin Oncol 1984; 2: 1343-1351 https://www.ncbi.nlm.nih.gov/pubmed/6096517
- 523 Jett JR, Everson L, Therneau TM. et al. Treatment of limited-stage small-cell lung cancer with cyclophosphamide, doxurubicin, and vincristine with or without etoposide: a randomized trial of the North Central Cancer Treatment Group. J Clin Oncol 1990; 8: 33-38 https://www.ncbi.nlm.nih.gov/pubmed/2153193
- 524 Goodman GE, Crowley JJ, Blasko JC. et al. Treatment of limited small-cell lung cancer with etoposide and cisplatin alternating with vincristine, doxorubicin, and cyclophosphamide versus concurrent etoposide, vincristine, doxorubicin, and cyclophosphamide and chest radiotherapy: a Southwest Oncology Group Study. J Clin Oncol 1990; 8: 39-47 https://www.ncbi.nlm.nih.gov/pubmed/2153194
- 525 Fukuoka M, Furuse K, Saijo N. et al. Randomized trial of cyclophosphamide, doxorubicin, and vincristine versus cisplatin and etoposide versus alternation of these regimens in small-cell lung cancer. J Natl Cancer Inst 1991; 83: 855-861 https://www.ncbi.nlm.nih.gov/pubmed/1648142
- 526 Skarlos DV, Samantas E, Kosmidis P. et al. Randomized comparison of etoposide-cisplatin vs etoposide-carboplatin and irradiation in small-cell lung cancer A Hellenic Co-operative Oncology Group study. Ann Oncol 1994; 5: 601-607 https://www.ncbi.nlm.nih.gov/pubmed/7993835
- 527 Lassen U, Kristjansen PE, Osterlind K. et al. Superiority of cisplatin or carboplatin in combination with teniposide and vincristine in the induction chemotherapy of small-cell lung cancer A randomized trial with 5 years follow up. Ann Oncol 1996; 7: 365-371 https://www.ncbi.nlm.nih.gov/pubmed/8805928
- 528 Hirsch FR, Osterlind K, Jeppesen N. et al. Superiority of high-dose platinum (cisplatin and carboplatin) compared to carboplatin alone in combination chemotherapy for small-cell lung carcinoma: a prospective randomised trial of 280 consecutive patients. Ann Oncol 2001; 12: 647-653 https://www.ncbi.nlm.nih.gov/pubmed/11432623
- 529 Gregor A, Drings P, Burghouts J. et al. Randomized trial of alternating versus sequential radiotherapy/chemotherapy in limited-disease patients with small-cell lung cancer: a European Organization for Research and Treatment of Cancer Lung Cancer Cooperative Group Study. J Clin Oncol 1997; 15: 2840-2849 https://www.ncbi.nlm.nih.gov/pubmed/9256127
- 530 Perry MC, Eaton WL, Propert KJ. et al. Chemotherapy with or without radiation therapy in limited small-cell carcinoma of the lung. N Engl J Med 1987; 316: 912-918 https://www.ncbi.nlm.nih.gov/pubmed/3029592
- 531 Perry MC, Herndon JE, Eaton WL. et al. Thoracic radiation therapy added to chemotherapy for small-cell lung cancer: an update of Cancer and Leukemia Group B Study 8083. J Clin Oncol 1998; 16: 2466-2467 https://www.ncbi.nlm.nih.gov/pubmed/9667265
- 532 Lebeau B, Urban T, Brechot JM. et al. A randomized clinical trial comparing concurrent and alternating thoracic irradiation for patients with limited small cell lung carcinoma “Petites Cellules” Group. Cancer 1999; 86: 1480-1487 https://www.ncbi.nlm.nih.gov/pubmed/10526276
- 533 Ettinger DS, Berkey BA, Abrams RA. et al. Study of paclitaxel, etoposide, and cisplatin chemotherapy combined with twice-daily thoracic radiotherapy for patients with limited-stage small-cell lung cancer: a Radiation Therapy Oncology Group 9609 phase II study. J Clin Oncol 2005; 23: 4991-4998 https://www.ncbi.nlm.nih.gov/pubmed/15939930
- 534 Bremnes RM, Sundstrom S, Vilsvik J. et al. Multicenter phase II trial of paclitaxel, cisplatin, and etoposide with concurrent radiation for limited-stage small-cell lung cancer. J Clin Oncol 2001; 19: 3532-3538 https://www.ncbi.nlm.nih.gov/pubmed/11481360
- 535 Glisson B, Scott C, Komaki R. et al. Cisplatin, ifosfamide, oral etoposide, and concurrent accelerated hyperfractionated thoracic radiation for patients with limited small-cell lung carcinoma: results of radiation therapy oncology group trial 93-12. J Clin Oncol 2000; 18: 2990-2995 https://www.ncbi.nlm.nih.gov/pubmed/10944132
- 536 Hanna N, Ansari R, Fisher W. et al. Etoposide, ifosfamide and cisplatin (VIP) plus concurrent radiation therapy for previously untreated limited small cell lung cancer (SCLC): a Hoosier Oncology Group (HOG) phase II study. Lung Cancer 2002; 35: 293-297 https://www.ncbi.nlm.nih.gov/pubmed/11844604
- 537 Havemann K, Wolf M, Holle R. et al. Alternating versus sequential chemotherapy in small cell lung cancer A randomized German multicenter trial. Cancer 1987; 59: 1072-1082 https://www.ncbi.nlm.nih.gov/pubmed/3028596
- 538 Wolf M, Pritsch M, Drings P. et al. Cyclic-alternating versus response-oriented chemotherapy in small-cell lung cancer: a German multicenter randomized trial of 321 patients. J Clin Oncol 1991; 9: 614-624 https://www.ncbi.nlm.nih.gov/pubmed/1648598
- 539 Bunn PA, Lichter AS, Makuch RW. et al. Chemotherapy alone or chemotherapy with chest radiation therapy in limited stage small cell lung cancer A prospective, randomized trial. Ann Intern Med 1987; 106: 655-662 https://www.ncbi.nlm.nih.gov/pubmed/3032033
- 540 Kies MS, Mira JG, Crowley JJ. et al. Multimodal therapy for limited small-cell lung cancer: a randomized study of induction combination chemotherapy with or without thoracic radiation in complete responders; and with wide-field versus reduced-field radiation in partial responders: a Southwest Oncology Group Study. J Clin Oncol 1987; 5: 592-600 https://www.ncbi.nlm.nih.gov/pubmed/3031226
- 541 Medical Research Council Lung Cancer Working Party. Radiotherapy alone or with chemotherapy in the treatment of small-cell carcinoma of the lung. Medical Research Council Lung Cancer Working Party. Br J Cancer 1979; 40: 1-10 https://www.ncbi.nlm.nih.gov/pubmed/222312
- 542 Osterlind K, Hansen HH, Hansen HS. et al. Chemotherapy versus chemotherapy plus irradiation in limited small cell lung cancer Results of a controlled trial with 5 years follow-up. Br J Cancer 1986; 54: 7-17 https://www.ncbi.nlm.nih.gov/pubmed/3015184
- 543 Perez CA, Einhorn L, Oldham RK. et al. Randomized trial of radiotherapy to the thorax in limited small-cell carcinoma of the lung treated with multiagent chemotherapy and elective brain irradiation: a preliminary report. J Clin Oncol 1984; 2: 1200-1208 https://www.ncbi.nlm.nih.gov/pubmed/6092555
- 544 Souhami RL, Geddes DM, Spiro SG. et al. Radiotherapy in small cell cancer of the lung treated with combination chemotherapy: a controlled trial. Br Med J (Clin Res.Ed) 1984; 288: 1643-1646 https://www.ncbi.nlm.nih.gov/pubmed/6326932
- 545 Pignon JP, Arriagada R, Ihde DC. et al. A meta-analysis of thoracic radiotherapy for small-cell lung cancer. N Engl J Med 1992; 327: 1618-1624 https://www.ncbi.nlm.nih.gov/pubmed/1331787
- 546 Warde P, Payne D. Does thoracic irradiation improve survival and local control in limited-stage small-cell carcinoma of the lung? A meta-analysis. J Clin Oncol 1992; 10: 890-895 https://www.ncbi.nlm.nih.gov/pubmed/1316951
- 547 Videtic GM, Stitt LW, Dar AR. et al. Continued cigarette smoking by patients receiving concurrent chemoradiotherapy for limited-stage small-cell lung cancer is associated with decreased survival. J Clin Oncol 2003; 21: 1544-1549 https://www.ncbi.nlm.nih.gov/pubmed/12697879
- 548 McCracken JD, Janaki LM, Crowley JJ. et al. Concurrent chemotherapy/radiotherapy for limited small-cell lung carcinoma: a Southwest Oncology Group Study. J Clin Oncol 1990; 8: 892-898 https://www.ncbi.nlm.nih.gov/pubmed/2159055
- 549 Thomas CR, Giroux DJ, Janaki LM. et al. Ten-year follow-up of Southwest Oncology Group 8269: a phase II trial of concomitant cisplatin-etoposide and daily thoracic radiotherapy in limited small-cell lung cancer. Lung Cancer 2001; 33: 213-219 https://www.ncbi.nlm.nih.gov/pubmed/11551416
- 550 Takada M, Fukuoka M, Kawahara M. et al. Phase III study of concurrent versus sequential thoracic radiotherapy in combination with cisplatin and etoposide for limited-stage small-cell lung cancer: results of the Japan Clinical Oncology Group Study 9104. J Clin Oncol 2002; 20: 3054-3060 https://www.ncbi.nlm.nih.gov/pubmed/12118018
- 551 Coy P, Hodson I, Payne DG. et al. The effect of dose of thoracic irradiation on recurrence in patients with limited stage small cell lung cancer Initial results of a Canadian Multicenter Randomized Trial. Int J Radiat Oncol Biol Phys 1988; 14: 219-226 https://www.ncbi.nlm.nih.gov/pubmed/2828289
- 552 Choi NC, Herndon JE, Rosenman J. et al. Phase I study to determine the maximum-tolerated dose of radiation in standard daily and hyperfractionated-accelerated twice-daily radiation schedules with concurrent chemotherapy for limited-stage small-cell lung cancer. J Clin Oncol 1998; 16: 3528-3536 https://www.ncbi.nlm.nih.gov/pubmed/9817271
- 553 Bogart JA, Herndon JE, Lyss AP. et al. 70 Gy thoracic radiotherapy is feasible concurrent with chemotherapy for limited-stage small-cell lung cancer: analysis of Cancer and Leukemia Group B study 39808. Int J Radiat Oncol Biol Phys 2004; 59: 460-468 https://www.ncbi.nlm.nih.gov/pubmed/15145163
- 554 Komaki R, Swann RS, Ettinger DS. et al. Phase I study of thoracic radiation dose escalation with concurrent chemotherapy for patients with limited small-cell lung cancer: Report of Radiation Therapy Oncology Group (RTOG) protocol 97-12. Int J Radiat Oncol Biol Phys 2005; 62: 342-350 https://www.ncbi.nlm.nih.gov/pubmed/15890573
- 555 Bonner JA, Sloan JA, Shanahan TG. et al. Phase III comparison of twice-daily split-course irradiation versus once-daily irradiation for patients with limited stage small-cell lung carcinoma. J Clin Oncol 1999; 17: 2681-2691 https://www.ncbi.nlm.nih.gov/pubmed/10561342
- 556 Schild SE, Bonner JA, Shanahan TG. et al. Long-term results of a phase III trial comparing once-daily radiotherapy with twice-daily radiotherapy in limited-stage small-cell lung cancer. Int J Radiat Oncol Biol Phys 2004; 59: 943-951 https://www.ncbi.nlm.nih.gov/pubmed/15234027
- 557 Shaw AT, Kim TM, Crinò L. et al. Ceritinib versus chemotherapy in patients with ALK-rearranged non-small-cell lung cancer previously given chemotherapy and crizotinib (ASCEND-5): a randomised, controlled, open-label, phase 3 trial. The Lancet Oncology 2017; 18: 874-886 https://doi.org/10.1016/S1470-2045(17)30339-X
- 558 Faivre-Finn C, Snee M, Ashcroft L. et al. Concurrent once-daily versus twice-daily chemoradiotherapy in patients with limited-stage small-cell lung cancer (CONVERT): an open-label, phase 3, randomised, superiority trial. Lancet Oncol 2017; 18: 1116-1125
- 559 Grønberg BH, Halvorsen TO, Fløtten Ø. et al. Randomized phase II trial comparing twice daily hyperfractionated with once daily hypofractionated thoracic radiotherapy in limited disease small cell lung cancer. Acta Oncol 2016; 55: 591-597
- 560 Yin X, Yan D, Qiu M. et al. Prophylactic cranial irradiation in small cell lung cancer: a systematic review and meta-analysis. BMC Cancer 2019; 19: 95 https://pubmed.ncbi.nlm.nih.gov/30665432/
- 561 Arriagada R, Le Péchoux CT, Riviere A. et al. Patterns of failure after prophylactic cranial irradiation in small-cell lung cancer: analysis of 505 randomized patients. Ann Oncol 2002; 13: 748-754 https://www.ncbi.nlm.nih.gov/pubmed/12075744
- 562 Auperin A, Arriagada R, Pignon JP. et al. Prophylactic cranial irradiation for patients with small-cell lung cancer in complete remission Prophylactic Cranial Irradiation Overview Collaborative Group. N Engl J Med 1999; 341: 476-484 https://www.ncbi.nlm.nih.gov/pubmed/10441603
- 563 Meert AP, Paesmans M, Berghmans T. et al. Prophylactic cranial irradiation in small cell lung cancer: a systematic review of the literature with meta-analysis. BMC Cancer 2001; 1: 5 https://www.ncbi.nlm.nih.gov/pubmed/11432756
- 564 Le Pechoux C, Dunant A, Senan S. et al. Standard-dose versus higher-dose prophylactic cranial irradiation (PCI) in patients with limited-stage small-cell lung cancer in complete remission after chemotherapy and thoracic radiotherapy (PCI 99-01, EORTC 22003-08004, RTOG 0212, and IFCT 99-01): a randomised clinical trial. Lancet Oncol 2009; 10: 467-474 https://www.ncbi.nlm.nih.gov/pubmed/19386548
- 565 Sun Y, Zhai C, Chen X. et al. Characterization of PD-L1 protein expression and CD8. Transl Lung Cancer Res 2019; 8: 748-759 https://pubmed.ncbi.nlm.nih.gov/32010554/
- 566 Cai H, Zhang H, Jiang Y. Prognostic and Clinicopathological Value of Programmed Cell Death Ligand1 Expression in Patients With Small Cell Lung Cancer: A Meta-Analysis. Front Oncol 2020; 10: 1079 https://pubmed.ncbi.nlm.nih.gov/32670887/
- 567 Horita N, Yamamoto M, Sato T. et al. Topotecan for Relapsed Small-cell Lung Cancer: Systematic Review and Meta-Analysis of 1347 Patients. Sci Rep 2015; 5: 15437 https://pubmed.ncbi.nlm.nih.gov/26486755/
- 568 Kakolyris S, Mavroudis D, Tsavaris N. et al. Paclitaxel in combination with carboplatin as salvage treatment in refractory small-cell lung cancer (SCLC): a multicenter phase II study. Ann Oncol 2001; 12: 193-197 https://www.ncbi.nlm.nih.gov/pubmed/11300323
- 569 Masuda N, Matsui K, Negoro S. et al. Combination of irinotecan and etoposide for treatment of refractory or relapsed small-cell lung cancer. J Clin Oncol 1998; 16: 3329-3334 https://www.ncbi.nlm.nih.gov/pubmed/9779709
- 570 O’Brien ME, Ciuleanu TE, Tsekov H. et al. Phase III trial comparing supportive care alone with supportive care with oral topotecan in patients with relapsed small-cell lung cancer. J Clin Oncol 2006; 24: 5441-5447 https://www.ncbi.nlm.nih.gov/pubmed/17135646
- 571 Groen HJ, Fokkema E, Biesma B. et al. Paclitaxel and carboplatin in the treatment of small-cell lung cancer patients resistant to cyclophosphamide, doxorubicin, and etoposide: a non-cross-resistant schedule. J Clin Oncol 1999; 17: 927-932 https://www.ncbi.nlm.nih.gov/pubmed/10071286
- 572 Kosmas C, Tsavaris NB, Malamos NA. et al. Phase II study of paclitaxel, ifosfamide, and cisplatin as second-line treatment in relapsed small-cell lung cancer. J Clin Oncol 2001; 19: 119-126 https://www.ncbi.nlm.nih.gov/pubmed/11134204
- 573 Naka N, Kawahara M, Okishio K. et al. Phase II study of weekly irinotecan and carboplatin for refractory or relapsed small-cell lung cancer. Lung Cancer 2002; 37: 319-323 https://www.ncbi.nlm.nih.gov/pubmed/12234702
- 574 von Pawel J, Schiller JH, Shepherd FA. et al. Topotecan versus cyclophosphamide, doxorubicin, and vincristine for the treatment of recurrent small-cell lung cancer. J Clin Oncol 1999; 17: 658-667 https://www.ncbi.nlm.nih.gov/pubmed/10080612
- 575 von Pawel J, Gatzemeier U, Pujol JL. et al. Phase ii comparator study of oral versus intravenous topotecan in patients with chemosensitive small-cell lung cancer. J Clin Oncol 2001; 19: 1743-1749 https://www.ncbi.nlm.nih.gov/pubmed/11251005
- 576 Eckardt JR, von Pawel J, Pujol JL. et al. Phase III study of oral compared with intravenous topotecan as second-line therapy in small-cell lung cancer. J Clin Oncol 2007; 25: 2086-2092 https://www.ncbi.nlm.nih.gov/pubmed/17513814
- 577 Takahashi T, Yamanaka T, Seto T. et al. Prophylactic cranial irradiation versus observation in patients with extensive-disease small-cell lung cancer: a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol 2017; 18: 663-671 https://pubmed.ncbi.nlm.nih.gov/28343976/
- 578 Gondi V, Pugh S, Tome W. et al. Preservation of memory with conformal avoidance of the hippocampal neural stem-cell compartment during whole-brain radiotherapy for brain metastases (RTOG 0933): a phase II multi-institutional trial. J Clin Oncol 2014; 32: 3810-3816 https://pubmed.ncbi.nlm.nih.gov/25349290/
- 579 De Dios NR, Murcia M, Counago F. et al. Phase III Trial of Prophylactic Cranial Irradiation with or without Hippocampal Avoidance for SMALL-CELL LUNG Cancer. International Journal of Radiation Oncology, Biology, Physics 2019; 105: S35 https://doi.org/10.1016/j.ijrobp.2019.06.451
- 580 Kristensen CA, Kristjansen PE, Hansen HH. Systemic chemotherapy of brain metastases from small-cell lung cancer: a review. J Clin Oncol 1992; 10: 1498-1502 https://www.ncbi.nlm.nih.gov/pubmed/1325541
- 581 Seute T, Leffers P, Wilmink JT. et al. Response of asymptomatic brain metastases from small-cell lung cancer to systemic first-line chemotherapy. J Clin Oncol 2006; 24: 2079-2083 https://www.ncbi.nlm.nih.gov/pubmed/16648509
- 582 Postmus PE, Haaxma-Reiche H, Smit EF. et al. Treatment of brain metastases of small-cell lung cancer: comparing teniposide and teniposide with whole-brain radiotherapy – a phase III study of the European Organization for the Research and Treatment of Cancer Lung Cancer Cooperative Group. J Clin Oncol 2000; 18: 3400-3408 https://www.ncbi.nlm.nih.gov/pubmed/11013281
- 583 Horneber M, Büschel G, Kaiser G. et al. Unkonventionelle Verfahren – Chancen für die Arzt-Patient-Beziehung. Der Onkologe 2003; 9: 1335-1342
- 584 Cassileth BR. Alternative and Complementary Cancer Treatments. Oncologist 1996; 1: 173-179
- 585 Vickers AJ, Kuo J, Cassileth BR. Unconventional anticancer agents: a systematic review of clinical trials. J Clin Oncol 2006; 24: 136-140 https://www.ncbi.nlm.nih.gov/pubmed/16382123
- 586 Parshall MB, Schwartzstein RM, Adams L. et al. An official American Thoracic Society statement: update on the mechanisms, assessment, and management of dyspnea. Am J Respir Crit Care Med 2012; 185: 435-452 https://www.ncbi.nlm.nih.gov/pubmed/22336677
- 587 Hui D, Bruera E. Integrating palliative care into the trajectory of cancer care. Nat Rev Clin Oncol 2016; 13: 159-71 https://pubmed.ncbi.nlm.nih.gov/26598947/
- 588 Pinna R, Campus G, Cumbo E. et al. Xerostomia induced by radiotherapy: an overview of the physiopathology, clinical evidence, and management of the oral damage. Ther Clin Risk Manag 2015; 11: 171-188 https://pubmed.ncbi.nlm.nih.gov/25691810/
- 589 Simon K. Colorectal cancer development and advances in screening. Clin Interv Aging 2016; 11: 967-976 https://pubmed.ncbi.nlm.nih.gov/27486317/
- 590 Barnes H, McDonald J, Smallwood N. et al. Opioids for the palliation of refractory breathlessness in adults with advanced disease and terminal illness. Cochrane Database Syst Rev 2016; 3: CD011008 https://pubmed.ncbi.nlm.nih.gov/27030166/
- 591 Ekström M, Bajwah S, Bland J. et al. One evidence base; three stories: do opioids relieve chronic breathlessness?. Thorax 2018; 73: 88-90 https://pubmed.ncbi.nlm.nih.gov/28377491/
- 592 Abernethy AP, Wheeler JL. Total dyspnoea. Curr Opin Support Palliat Care 2008; 2: 110-113 https://www.ncbi.nlm.nih.gov/pubmed/18685406
- 593 Allard P, Lamontagne C, Bernard P. et al. How effective are supplementary doses of opioids for dyspnea in terminally ill cancer patients? A randomized continuous sequential clinical trial. J Pain Symptom Manage 1999; 17: 256-265
- 594 Bruera E, Sala R, Spruyt O. et al. Nebulized versus subcutaneous morphine for patients with cancer dyspnea: a preliminary study. Journal of Pain & Symptom Management 2005; 29: 613-618
- 595 Charles MA, Reymond L, Israel F. Relief of incident dyspnea in palliative cancer patients: A pilot, randomized, controlled trial comparing nebulized hydromorphone, systemic hydromorphone, and nebulized saline. Journal of Pain and Symptom Management 2008; 36: 29-38
- 596 Grimbert D, Lubin O, de Monte M. et al. [Dyspnea and morphine aerosols in the palliative care of lung cancer]. Rev Mal Respir 2004; 21: 1091-7 https://www.ncbi.nlm.nih.gov/pubmed/15767953
- 597 Jennings AL, Davies AN, Higgins JP. et al. Opioids for the palliation of breathlessness in terminal illness. Cochrane Database Syst Rev 2001; CD002066 https://www.ncbi.nlm.nih.gov/pubmed/11687137
- 598 Jensen D, Alsuhail A, Viola R. et al. Inhaled Fentanyl Citrate Improves Dynamic Airway Function, Exertional Dyspnea And Exercise Endurance In COPD [Abstract]. American Journal of Respiratory and Critical Care Medicine 2011; A5627
- 599 Johnson MJ, McDonagh TA, Harkness A. et al. Morphine for the relief of breathlessness in patients with chronic heart failure – A pilot study. European journal of heart failure 2002; 4: 753-756 https://www.ncbi.nlm.nih.gov/pubmed/12453546
- 600 Mazzocato C, Buclin T, Rapin CH. The effects of morphine on dyspnea and ventilatory function in elderly patients with advanced cancer: A randomized double-blind controlled trial. Annals of Oncology 1999; 10: 1511-1514 https://www.ncbi.nlm.nih.gov/pubmed/10643545
- 601 Navigante AH, Cerchietti LC, Castro MA. et al. Midazolam as adjunct therapy to morphine in the alleviation of severe dyspnea perception in patients with advanced cancer. J Pain Symptom Manage 2006; 31: 38-47 https://www.ncbi.nlm.nih.gov/pubmed/16442481
- 602 Navigante AH, Castro MA, Cerchietti LeandroC. Morphine Versus Midazolam as Upfront Therapy to Control Dyspnea Perception in Cancer Patients While Its Underlying Cause Is Sought or Treated. Journal of pain and symptom management 2010; 39: 820-830 https://www.ncbi.nlm.nih.gov/pubmed/20471543
- 603 Oxberry SG, Torgerson DJ, Bland JM. et al. Short-term opioids for breathlessness in stable chronic heart failure: a randomized controlled trial. Eur J Heart Fail 2011; 13: 1006-1012 https://www.ncbi.nlm.nih.gov/pubmed/21712288
- 604 Verberkt C, van den Beuken-van Everdingen M, Schols J. et al. Respiratory adverse effects of opioids for breathlessness: a systematic review and meta-analysis. Eur Respir J 2017; 50 DOI: 10.1183/13993003.01153-2017. https://pubmed.ncbi.nlm.nih.gov/29167300/
- 605 Abernethy AP, Currow DC, Frith P. et al. Randomised, double blind, placebo controlled crossover trial of sustained release morphine for the management of refractory dyspnoea. BMJ 2003; 327: 523-528 https://www.ncbi.nlm.nih.gov/pubmed/12958109
- 606 Allard P, Lamontagne C, Bernard P. et al. How effective are supplementary doses of opioids for dyspnea in terminally ill cancer patients? A randomized continuous sequential clinical trial. J Pain Symptom Manage 1999; 17: 256-265 https://www.ncbi.nlm.nih.gov/pubmed/10203878
- 607 Bruera E, Sala R, Spruyt O. et al. Nebulized versus subcutaneous morphine for patients with cancer dyspnea: a preliminary study. Journal of Pain & Symptom Management 2005; 29: 613-618
- 608 Hardy A, Emsley R, Freeman D. et al. Psychological Mechanisms Mediating Effects Between Trauma and Psychotic Symptoms: The Role of Affect Regulation, Intrusive Trauma Memory, Beliefs, and Depression. Schizophr Bull 2016; 42 (Suppl. 01) S34-S43 https://pubmed.ncbi.nlm.nih.gov/27460616/
- 609 Simon ST, Higginson IJ, Booth S. et al. Benzodiazepines for the relief of breathlessness in advanced malignant and non-malignant diseases in adults. Cochrane Database Syst Rev 2010; CD007354
- 610 Stege G, Heijdra YF, van den Elshout FJ. et al. Temazepam 10mg does not affect breathing and gas exchange in patients with severe normocapnic COPD. Respir Med 2010; 104: 518-524 https://www.ncbi.nlm.nih.gov/pubmed/19910177
- 611 Raijmakers NJH, van Zuylen L, Costantini M. et al. Artificial nutrition and hydration in the last week of life in cancer patients A systematic literature review of practices and effects. Annals of Oncology 2011; 22: 1478-1486 https://www.ncbi.nlm.nih.gov/pubmed/21199887
- 612 Bruera E, Hui D, Dalal S. et al. Parenteral hydration in patients with advanced cancer: a multicenter, double-blind, placebo-controlled randomized trial. J Clin Oncol 2013; 31: 111-118 https://www.ncbi.nlm.nih.gov/pubmed/23169523
- 613 Nakajima N, Hata Y, Kusumuto K. A clinical study on the influence of hydration volume on the signs of terminally ill cancer patients with abdominal malignancies. J Palliat Med 2013; 16: 185-189 https://www.ncbi.nlm.nih.gov/pubmed/23327196
- 614 Lübbe AS. Prinzipien und Standards der onkologischen Rehabilitation. TumorDiagn u Ther 2004; 25: 65-71
- 615 Lübbe AS. Konzepte onkologischer Rehabilitation. Therapiekonzepte Onkologie 2003 https://link.springer.com/chapter/10.1007/978-3-662-10493-4_65
- 616 Fialka-Moser V, Crevenna R, Korpan M. et al. Cancer rehabilitation: particularly with aspects on physical impairments. J Rehabil Med 2003; 35: 153-162 https://www.ncbi.nlm.nih.gov/pubmed/12892240
- 617 Nazarian J. Cardiopulmonary rehabilitation after treatment for lung cancer. Curr Treat Options Oncol 2004; 5: 75-82 https://www.ncbi.nlm.nih.gov/pubmed/14697159
- 618 Spruit MA, Janssen PP, Willemsen SC. et al. Exercise capacity before and after an 8-week multidisciplinary inpatient rehabilitation program in lung cancer patients: a pilot study. Lung Cancer 2006; 52: 257-260 https://www.ncbi.nlm.nih.gov/pubmed/16529844
- 619 Thompson E, Sola I, Subirana M. Non-invasive interventions for improving well-being and quality of life in patients with lung cancer – a systematic review of the evidence. Lung Cancer 2005; 50: 163-176 https://www.ncbi.nlm.nih.gov/pubmed/16137786
- 620 Sola I, Thompson E, Subirana M. et al. Non-invasive interventions for improving well-being and quality of life in patients with lung cancer (Review). The Cochrane Library, Issue 1 2007 https://www.ncbi.nlm.nih.gov/pubmed/16137786
- 621 Bredin M, Corner J, Krishnasamy M. et al. Multicentre randomised controlled trial of nursing intervention for breathlessness in patients with lung cancer. BMJ 1999; 318: 901-904 https://www.ncbi.nlm.nih.gov/pubmed/10102851
- 622 Christman NJ, Cain LB. The effects of concrete objective information and relaxation on maintaining usual activity during radiation therapy. Oncol Nurs Forum 2004; 31: E39-E45 https://www.ncbi.nlm.nih.gov/pubmed/15017453
- 623 Doorenbos A, Given B, Given C. et al. Physical functioning: effect of behavioral intervention for symptoms among individuals with cancer. Nurs Res 2006; 55: 161-171 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2012950/
- 624 Dimeo FC, Tilmann MH, Bertz H. et al. Aerobic exercise in the rehabilitation of cancer patients after high dose chemotherapy and autologous peripheral stem cell transplantation. Cancer 1997; 79: 1717-1722 https://www.ncbi.nlm.nih.gov/pubmed/9128987
- 625 Dimeo FC, Stieglitz RD, Novelli-Fischer U. et al. Effects of physical activity on the fatigue and psychologic status of cancer patients during chemotherapy. Cancer 1999; 85: 2273-2277 https://www.ncbi.nlm.nih.gov/pubmed/10326708
- 626 Dimeo FC, Thomas F, Raabe-Menssen C. et al. Effect of aerobic exercise and relaxation training on fatigue and physical performance of cancer patients after surgery A randomised controlled trial. Support Care Cancer 2004; 12: 774-779 https://www.ncbi.nlm.nih.gov/pubmed/15338385
- 627 Schultz K, Bergmann KC, Kenn K. et al. Effektivit„t der pneumologischen Anschluss-Rehabilitation (AHB). Dtsch Med Wochenschr 2006; 131: 1793-1798
- 628 Riesenberg H, Lübbe AS. Prädiktoren und Outcome stationärer Rehabilitation bei Patienten mit Bronchialkarzinom. TumorDiagnostik und Therapie 2007; 28: 279-284
- 629 Egermann U, Jaeggi K, Habicht JM. et al. Regular follow-up after curative resection of nonsmall cell lung cancer: a real benefit for patients?. Eur Respir J 2002; 19: 464-468 https://www.ncbi.nlm.nih.gov/pubmed/11936523
- 630 Pisters KM, Le Chevalier T. Adjuvant chemotherapy in completely resected non-small-cell lung cancer. J Clin Oncol 2005; 23: 3270-3278 https://www.ncbi.nlm.nih.gov/pubmed/15886314
- 631 Martini N, Bains MS, Burt ME. et al. Incidence of local recurrence and second primary tumors in resected stage I lung cancer. J Thorac Cardiovasc Surg 1995; 109: 120-129 https://www.ncbi.nlm.nih.gov/pubmed/7815787
- 632 Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft DKG. Entwicklung von leitlinienbasierten Qualitätsindikatoren Methodenpapier für das Leitlinienprogramm Onkologie, Version 30 2021. 2021 https://www.leitlinienprogramm-onkologie.de/methodik/grundlegende-informationen-zur-methodik/