CC BY-NC-ND 4.0 · Endosc Int Open 2024; 12(03): E361-E366
DOI: 10.1055/a-2257-3171
Original article

Comparison of endoscopic ultrasound-guided fine-needle aspiration and fine-needle biopsy to generate pancreatic cancer organoids: Randomized trial

1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Felix Orben
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Arlett Schäfer
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Lisa Fricke
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Günter Schneider
2   Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Gottingen, Germany (Ringgold ID: RIN27177)
3   Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Chair of Translational Cancer Research and Institute of Experimental Cancer Therapy, München, Germany
4   CCC-N (Comprehensive Cancer Center Lower Saxony), Medizinische Hochschule Hannover, Hannover, Germany (Ringgold ID: RIN9177)
,
Maximilian Reichert
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
5   Translational Pancreatic Cancer Center, Medical Clinic and Polyclinic II, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
6   German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Partner Site Munich, DKFZ, Heidelberg, Germany (Ringgold ID: RIN28333)
7   Center for Protein Assemblies (CPA), Technical University of Munich, 85747, Garching, Germany (Ringgold ID: RIN9184)
,
Alexander Herner
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
8   Department of Gastroenterology and Hepatology, University Hospital Zurich, Zürich, Switzerland (Ringgold ID: RIN27243)
,
Ulrich Mayr
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Veit Phillip
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Matthias Treiber
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Guido von Figura
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Mohamed Abdelhafez
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Roland M. Schmid
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
,
Christoph Schlag
8   Department of Gastroenterology and Hepatology, University Hospital Zurich, Zürich, Switzerland (Ringgold ID: RIN27243)
1   Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, München, Germany (Ringgold ID: RIN9184)
› Author Affiliations
Supported by: Deutsche Forschungsgemeinschaft SFB1321 (Project-ID 329628492), RE 3723/4-1
Supported by: Deutsche Krebshilfe Max-Eder Program 111273 and 70114328

Clinical Trial: Registration number (trial ID): NCT03990675, Trial registry: ClinicalTrials.gov (http://www.clinicaltrials.gov/), Type of Study: Prospective randomized

Abstract

Background and study aims The prognosis for pancreatic cancer remains poor. Molecular diagnostics and customized therapies are becoming increasingly important in clinical routine. Patient-derived, predictive model systems such as organoids have the potential to substantially increase the depth of information from biopsy material by functional and molecular characterization. We compared the extent to which the use of fine-needle aspiration needles (FNA, 22G) or fine-needle biopsy needles (FNB, 22G) influences the generation of pancreatic cancer patient-derived organoids (PDOs) to establish endoscopic standards of organoid technology.

Patients and methods Endoscopic ultrasound (EUS)-guided punctures by EUS-FNA and EUS-FNB of pancreatic masses highly suspicious for adenocarcinoma (detected by computed tomography and/or magnetic resonance imaging) were prospectively evaluated. Consecutive patients received EUS-FNA and EUS-FNB in a randomized order without the need to exchange the needle shaft (only the inner needle type (FNA/-B) was exchanged) between the passes. With each needle type, the specimens for histological analysis and for PDOs were obtained separately.

Results Fifty patients were enrolled in the study. Histology revealed malignancy in 42 of 50 cases (84%). In total PDOs were generated from 17 patients (34%). Of these, nine were established by FNB only, two by FNA only, and six by both FNA and FNB. Histology revealed malignancy in 13 of 17 PDO cases (76%). In two histologically false-negative cases, PDOs could be established.

Conclusions EUS-FNB was superior to EUS-FNA in terms of successful generation of PDOs, although it failed to show statistical significance.



Publication History

Received: 18 July 2023

Accepted after revision: 19 December 2023

Article published online:
07 March 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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