Pitfalls in assessing stromal tumor infiltrating lymphocytes (sTILs) in breast cancer

Author:

Kos Zuzana, ,Roblin Elvire,Kim Rim S.,Michiels Stefan,Gallas Brandon D.ORCID,Chen Weijie,van de Vijver Koen K.ORCID,Goel Shom,Adams Sylvia,Demaria SandraORCID,Viale Giuseppe,Nielsen Torsten O.,Badve Sunil S.ORCID,Symmans W. FraserORCID,Sotiriou Christos,Rimm David L.ORCID,Hewitt Stephen,Denkert Carsten,Loibl Sibylle,Luen Stephen J.,Bartlett John M. S.,Savas PeterORCID,Pruneri Giancarlo,Dillon Deborah A.,Cheang Maggie Chon U.,Tutt Andrew,Hall Jacqueline A.ORCID,Kok Marleen,Horlings Hugo M.ORCID,Madabhushi Anant,van der Laak JeroenORCID,Ciompi Francesco,Laenkholm Anne-Vibeke,Bellolio EnriqueORCID,Gruosso Tina,Fox Stephen B.,Araya Juan CarlosORCID,Floris GiuseppeORCID,Hudeček JanORCID,Voorwerk Leonie,Beck Andrew H.,Kerner Jen,Larsimont Denis,Declercq Sabine,Van den Eynden Gert,Pusztai Lajos,Ehinger AnnaORCID,Yang Wentao,AbdulJabbar Khalid,Yuan Yinyin,Singh Rajendra,Hiley Crispin,Bakir Maise al,Lazar Alexander J.ORCID,Naber Stephen,Wienert Stephan,Castillo MiluskaORCID,Curigliano GiuseppeORCID,Dieci Maria-Vittoria,André Fabrice,Swanton Charles,Reis-Filho Jorge,Sparano JosephORCID,Balslev Eva,Chen I-Chun,Stovgaard Elisabeth Ida Specht,Pogue-Geile Katherine,Blenman Kim R. M.,Penault-Llorca Frédérique,Schnitt Stuart,Lakhani Sunil R.,Vincent-Salomon Anne,Rojo Federico,Braybrooke Jeremy P.ORCID,Hanna Matthew G.ORCID,Soler-Monsó M. Teresa,Bethmann Daniel,Castaneda Carlos A.,Willard-Gallo KarenORCID,Sharma AshishORCID,Lien Huang-Chun,Fineberg Susan,Thagaard Jeppe,Comerma LauraORCID,Gonzalez-Ericsson PaulaORCID,Brogi Edi,Loi ShereneORCID,Saltz Joel,Klaushen Frederick,Cooper LeeORCID,Amgad Mohamed,Moore David A.,Salgado Roberto

Abstract

AbstractStromal tumor-infiltrating lymphocytes (sTILs) are important prognostic and predictive biomarkers in triple-negative (TNBC) and HER2-positive breast cancer. Incorporating sTILs into clinical practice necessitates reproducible assessment. Previously developed standardized scoring guidelines have been widely embraced by the clinical and research communities. We evaluated sources of variability in sTIL assessment by pathologists in three previous sTIL ring studies. We identify common challenges and evaluate impact of discrepancies on outcome estimates in early TNBC using a newly-developed prognostic tool. Discordant sTIL assessment is driven by heterogeneity in lymphocyte distribution. Additional factors include: technical slide-related issues; scoring outside the tumor boundary; tumors with minimal assessable stroma; including lymphocytes associated with other structures; and including other inflammatory cells. Small variations in sTIL assessment modestly alter risk estimation in early TNBC but have the potential to affect treatment selection if cutpoints are employed. Scoring and averaging multiple areas, as well as use of reference images, improve consistency of sTIL evaluation. Moreover, to assist in avoiding the pitfalls identified in this analysis, we developed an educational resource available at www.tilsinbreastcancer.org/pitfalls.

Funder

Breast Cancer Research Foundation

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Radiology, Nuclear Medicine and imaging,Oncology

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