Pitfalls in machine learning-based assessment of tumor-infiltrating lymphocytes in breast cancer: A report of the International Immuno-Oncology Biomarker Working Group on Breast Cancer

  • Jeppe Thagaard
  • , Glenn Broeckx
  • , David B Page
  • , Chowdhury Arif Jahangir
  • , Sara Verbandt
  • , Zuzana Kos
  • , Rajarsi Gupta
  • , Reena Khiroya
  • , Khalid Abduljabbar
  • , Gabriela Acosta Haab
  • , Balazs Acs
  • , Guray Akturk
  • , Jonas S Almeida
  • , Isabel Alvarado-Cabrero
  • , Mohamed Amgad
  • , Farid Azmoudeh-Ardalan
  • , Sunil S. Badve
  • , Nurkhairul Bariyah Baharun
  • , Eva Balslev
  • , Enrique R Bellolio
  • Vydehi Bheemaraju, Kim Rm Blenman, Luciana Botinelly Mendonça Fujimoto, Najat Bouchmaa, Octavio Burgues, Alexandros Chardas, Maggie Chon U Cheang, Francesco Ciompi, Lee Ad Cooper, An Coosemans, Germán Corredor, Anders B Dahl, Flavio Luis Dantas Portela, Frederik Deman, Sandra Demaria, Johan Doré Hansen, Sarah N Dudgeon, Thomas Ebstrup, Mahmoud Elghazawy, Claudio Fernandez-Martín, Stephen B Fox, William M Gallagher, Jennifer M Giltnane, Sacha Gnjatic, Paula I Gonzalez-Ericsson, Anita Grigoriadis, Niels Halama, Matthew G Hanna, Aparna Harbhajanka, Steven N Hart, Johan Hartman, Søren Hauberg, Stephen Hewitt, Akira I Hida, Hugo M Horlings, Zaheed Husain, Evangelos Hytopoulos, Sheeba Irshad, Emiel Am Janssen, Mohamed Kahila, Tatsuki R Kataoka, Kosuke Kawaguchi, Durga Kharidehal, Andrey I Khramtsov, Umay Kiraz, Pawan Kirtani, Liudmila L Kodach, Konstanty Korski, Anikó Kovács, Anne-Vibeke Laenkholm, Corinna Lang-Schwarz, Denis Larsimont, Jochen K Lennerz, Marvin Lerousseau, Xiaoxian Li, Amy Ly, Anant Madabhushi, Sai K Maley, Vidya Manur Narasimhamurthy, Douglas K Marks, Elizabeth S McDonald, Ravi Mehrotra, Stefan Michiels, Fayyaz Ul Amir Afsar Minhas, Shachi Mittal, David A Moore, Shamim Mushtaq, Hussain Nighat, Thomas Papathomas, Frederique Penault-Llorca, Rashindrie D Perera, Christopher J Pinard, Juan Carlos Pinto-Cardenas, Giancarlo Pruneri, Lajos Pusztai, Arman Rahman, Nasir Mahmood Rajpoot, Bernardo Leon Rapoport, Tilman T Rau, Jorge S Reis-Filho, Joana M Ribeiro, David Rimm, Anne Roslind, Anne Vincent-Salomon, Manuel Salto-Tellez, Joel Saltz, Shahin Sayed, Ely Scott, Kalliopi P Siziopikou, Christos Sotiriou, Albrecht Stenzinger, Maher A Sughayer, Daniel Sur, Susan Fineberg, Fraser Symmans, Sunao Tanaka, Timothy Taxter, Sabine Tejpar, Jonas Teuwen, E Aubrey Thompson, Trine Tramm, William T Tran, Jeroen van der Laak, Paul J van Diest, Gregory E Verghese, Giuseppe Viale, Michael Vieth, Noorul Wahab, Thomas Walter, Yannick Waumans, Hannah Y Wen, Wentao Yang, Yinyin Yuan, Reena Md Zin, Sylvia Adams, John Bartlett, Sibylle Loibl, Carsten Denkert, Peter Savas, Sherene Loi, Roberto Salgado, Elisabeth Specht Stovgaard*
*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftReviewForskningpeer review

Abstract

The clinical significance of the tumor-immune interaction in breast cancer is now established, and tumor-infiltrating lymphocytes (TILs) have emerged as predictive and prognostic biomarkers for patients with triple-negative (estrogen receptor, progesterone receptor, and HER2-negative) breast cancer and HER2-positive breast cancer. How computational assessments of TILs might complement manual TIL assessment in trial and daily practices is currently debated. Recent efforts to use machine learning (ML) to automatically evaluate TILs have shown promising results. We review state-of-the-art approaches and identify pitfalls and challenges of automated TIL evaluation by studying the root cause of ML discordances in comparison to manual TIL quantification. We categorize our findings into four main topics: (1) technical slide issues, (2) ML and image analysis aspects, (3) data challenges, and (4) validation issues. The main reason for discordant assessments is the inclusion of false-positive areas or cells identified by performance on certain tissue patterns or design choices in the computational implementation. To aid the adoption of ML for TIL assessment, we provide an in-depth discussion of ML and image analysis, including validation issues that need to be considered before reliable computational reporting of TILs can be incorporated into the trial and routine clinical management of patients with triple-negative breast cancer. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

OriginalsprogEngelsk
Sider (fra-til)498-513
Antal sider16
TidsskriftJournal of Pathology
Vol/bind260
Udgave nummer5
DOI
StatusUdgivet - aug. 2023

Finansiering

BevillingsgivereBevillingsgivernummer
Gilead Sciences, Inc.
KU Leuven
Svenska Sällskapet för Medicinsk Forskning
Bröstcancerförbundet
United States Department of Defense
National Institutes of Health
Horizon 2020
National Health and Medical Research Council of Australia
Irish Cancer Society
Science Foundation Ireland
Science Foundation Ireland
National Institutes of Health
Breast Cancer Now
Cancer Research UK
Japan Society for the Promotion of Science
National Cancer InstituteP50CA247749, R01CA257612, U01CA269181, R01CA268287, U54CA254566, P30CA196521, R01CA268207, R01CA220581, P30CA008748, R01CA216579, U01CA248226, U24CA224319, P50CA116201, UH3CA225021, U24CA215109, R01CA208236, R01CA249992, R37CA225655, U01CA239055
National Heart, Lung, and Blood Institute
National Institute of Biomedical Imaging and Bioengineering
Department of Veterans Affairs
Bristol-Myers Squibb
Boehringer Ingelheim GmbH
Eli Lilly
AstraZeneca
Fondation ARC pour la recherche sur le cancer
Ligue Contre le Cancer
University of Melbourne
Peter Maccallum Cancer Centre
Breast Cancer Research FoundationW81XWH-21-1-0160
Susan G. Komen
KU Leuven
Dutch Cancer Society
Ministry of Health, Welfare and Sport
Cancer Research UKGNT1193630
National Health and Medical Research Council of Australia
National Breast Cancer Foundation of AustraliaCCRC13GAL
Breast Cancer Research Foundation15/IA/3104
National Health and Medical Research Council of Australia18/SPP/3522
Breast Cancer Research FoundationCA224319, DK124165, CA263705, CA196521, R01CA268287A1
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