Transformer-based biomarker prediction from colorectal cancer histology: A large-scale multicentric study

Sophia J. Wagner(Helmholtz Zentrum München), Daniel Reisenbüchler(Center for Environmental Health), Nicholas P. West(Johannes Gutenberg University Mainz), Jan Niehues(Fresenius (Germany)), Jiefu Zhu(Fresenius (Germany)), Sebastian Foersch(Johannes Gutenberg University Mainz), Gregory Patrick Veldhuizen(Fresenius (Germany)), Philip Quirke(University of Leeds), Heike I. Grabsch(University of Leeds), Piet A. van den Brandt(Maastricht University), Gordon Hutchins(University of Leeds), Susan D. Richman(University of Leeds), Tanwei Yuan(German Cancer Research Center), Rupert Langer(Johannes Kepler University of Linz), Josien C.A. Jenniskens(Maastricht University), Kelly Offermans(Maastricht University), Wolfram Mueller(Praxis für Humangenetik), Richard Gray(University of Oxford), Stephen B. Gruber(City Of Hope National Medical Center), Joel K. Greenson(City of Hope), Gad Rennert(Technion – Israel Institute of Technology), Joseph D. Bonner(Technion – Israel Institute of Technology), Daniel Schmolze(City Of Hope National Medical Center), Jitendra Jonnagaddala(UNSW Sydney), Nicholas J. Hawkins(UNSW Sydney), Robyn L. Ward(The University of Sydney), Dion Morton(NIHR Surgical Reconstruction and Microbiology Research Centre), Michel Seymour(St James's University Hospital), Laura Magill(Cancer Research UK Clinical Trials Unit), Marta Nowak(University of Zurich), Jennifer Hay(Queen Elizabeth University Hospital), Viktor H. Koelzer(University of Zurich), David N. Church(University of Oxford), David N. Church(Helmholtz Zentrum München), Enric Domingo(Universitätsklinikum Erlangen), Joanne Edwards(Jinggangshan University), Bengt Glimelius(Second Affiliated Hospital of Guangzhou Medical University), Ismail Gögenür(Second Affiliated Hospital of Guangzhou Medical University), Andrea Harkin(Queen's University Belfast), Jen Hay(Queen's University Belfast), Timothy Iveson(Queen's University Belfast), Emma Jaeger(German Cancer Research Center), Caroline Kelly(German Cancer Research Center), Rachel Kerr(Helmholtz Zentrum München), Noori Maka(King's College London), Hannah Morgan(Technical University of Munich), Karin A. Oien(Helmholtz Zentrum München), Clare Orange(University of Leeds), Claire Palles(University of Oxford), Campbell S.D. Roxburgh, Owen J. Sansom, Mark Saunders, Ian Tomlinson, Christian Matek(Comprehensive Cancer Center Erlangen), Carol Geppert(Maastricht University), Chaolong Peng(Jinggangshan University), Cheng Zhi(Second Affiliated Hospital of Guangzhou Medical University), Xiaoming Ouyang(Maastricht University), Jacqueline A. James(Queen's University Belfast), Maurice B. Loughrey(Queen's University Belfast), Manuel Salto‐Tellez(Belfast Health and Social Care Trust), Hermann Brenner(German Cancer Research Center), Michael Hoffmeister(German Cancer Research Center), Daniel Truhn(RWTH Aachen University), Julia A. Schnabel(Helmholtz Zentrum München), Melanie Boxberg(Technical University of Munich), Tingying Peng(Helmholtz Zentrum München), Jakob Nikolas Kather(Johannes Gutenberg University Mainz)
Cancer Cell
August 30, 2023
Cited by 238Open Access
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Abstract

Deep learning (DL) can accelerate the prediction of prognostic biomarkers from routine pathology slides in colorectal cancer (CRC). However, current approaches rely on convolutional neural networks (CNNs) and have mostly been validated on small patient cohorts. Here, we develop a new transformer-based pipeline for end-to-end biomarker prediction from pathology slides by combining a pre-trained transformer encoder with a transformer network for patch aggregation. Our transformer-based approach substantially improves the performance, generalizability, data efficiency, and interpretability as compared with current state-of-the-art algorithms. After training and evaluating on a large multicenter cohort of over 13,000 patients from 16 colorectal cancer cohorts, we achieve a sensitivity of 0.99 with a negative predictive value of over 0.99 for prediction of microsatellite instability (MSI) on surgical resection specimens. We demonstrate that resection specimen-only training reaches clinical-grade performance on endoscopic biopsy tissue, solving a long-standing diagnostic problem.


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