Nuklearmedizin 2022; 61(06): 433-439
DOI: 10.1055/a-1868-4918
Original Article

IMPORTANCE of PRETREATMENT 18F-FDG PET/CT TEXTURE ANALYSIS in PREDICTING EGFR and ALK MUTATION in PATIENTS with NON-SMALL CELL LUNG CANCER

Bedeutung der Vorbehandlung bei 18F-FDG-PET/CT – Texturanalyse zur Vorhersage von EGFR- und ALK-Mutation bei Patient*innen mit nichtkleinzelligem Lungenkrebs
Nurşin Agüloğlu
,
Ayşegül Aksu
1   Bahçeşehir Çam ve Sakura Hastanesi, İstanbul, Turkey
,
Murat Akyol
,
Nuran Katgı
,
Tuğçe Çiftçi Doksöz
› Author Affiliations

Abstract

Objective Identification of anaplastic lymphoma kinase (ALK) and epidermal growth factor receptor (EGFR) mutation types is of great importance before treatment with tyrosine kinase inhibitors (TKIs). Radiomics is a new strategy for noninvasively predicting the genetic status of cancer. We aimed to evaluate the predictive power of 18F-FDG PET/CT-based radiomic features for mutational status before treatment in non-small cell lung cancer (NSCLC) and to develop a predictive model based on radiomic features.

Methods Images of patients who underwent 18F-FDG PET/CT for initial staging with the diagnosis of NSCLC between January 2015 and July 2020 were evaluated using LIFEx software. The region of interest (ROI) of the primary tumor was established and volumetric and textural features were obtained. Clinical data and radiomic data were evaluated with machine learning (ML) algorithms to create a model.

Results For EGFR mutation prediction, the most successful machine learning algorithm obtained with GLZLM_GLNU and clinical data was Naive Bayes (AUC: 0.751, MCC: 0.347, acc: 71.4%). For ALK rearrangement prediction, the most successful machine learning algorithm obtained with GLCM_correlation, GLZLM_LZHGE and clinical data was evaluated as Naive Bayes (AUC: 0.682, MCC: 0.221, acc: 77.4%).

Conclusions In our study, we created prediction models based on radiomic analysis of 18F-FDG PET/CT images. Tissue analysis with ML algorithms are non-invasive methods for predicting ALK rearrangement and EGFR mutation status in NSCLC, which may be useful for targeted therapy selection in a clinical setting.



Publication History

Received: 18 November 2021

Accepted after revision: 01 June 2022

Article published online:
17 August 2022

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