Prognostic Value of Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancers From Two Phase III Randomized Adjuvant Breast Cancer Trials: ECOG 2197 and ECOG 1199

Author:

Adams Sylvia1,Gray Robert J.1,Demaria Sandra1,Goldstein Lori1,Perez Edith A.1,Shulman Lawrence N.1,Martino Silvana1,Wang Molin1,Jones Vicky E.1,Saphner Thomas J.1,Wolff Antonio C.1,Wood William C.1,Davidson Nancy E.1,Sledge George W.1,Sparano Joseph A.1,Badve Sunil S.1

Affiliation:

1. Sylvia Adams and Sandra Demaria, New York University School of Medicine, New York; Joseph A. Sparano, Albert Einstein Medical Center, Bronx, NY; Robert J. Gray, Lawrence N. Shulman, and Molin Wang, Dana-Farber Cancer Institute, Boston, MA; Lori Goldstein, Fox Chase Cancer Center, Philadelphia; Nancy E. Davidson, University of Pittsburgh, Pittsburgh, PA; Edith A. Perez, Mayo Clinic, Jacksonville, FL; Silvana Martino, Angeles Clinic and Research Institute, Santa Monica; Vicky E. Jones, University of...

Abstract

Purpose Recent studies suggest that tumor-infiltrating lymphocytes (TILs) are associated with disease-free (DFS) and overall survival (OS) in operable triple-negative breast cancer (TNBC). We seek to validate the prognostic impact of TILs in primary TNBCs in two adjuvant phase III trials conducted by the Eastern Cooperative Oncology Group (ECOG). Patients and Methods Full-face hematoxylin and eosin–stained sections of 506 tumors from ECOG trials E2197 and E1199 were evaluated for density of TILs in intraepithelial (iTILs) and stromal compartments (sTILs). Patient cases of TNBC from E2197 and E1199 were randomly selected based on availability of sections. For the primary end point of DFS, association with TIL scores was determined by fitting proportional hazards models stratified on study. Secondary end points were OS and distant recurrence–free interval (DRFI). Reporting recommendations for tumor marker prognostic studies criteria were followed, and all analyses were prespecified. Results The majority of 481 evaluable cancers had TILs (sTILs, 80%; iTILs, 15%). With a median follow-up of 10.6 years, higher sTIL scores were associated with better prognosis; for every 10% increase in sTILs, a 14% reduction of risk of recurrence or death (P = .02), 18% reduction of risk of distant recurrence (P = .04), and 19% reduction of risk of death (P = .01) were observed. Multivariable analysis confirmed sTILs to be an independent prognostic marker of DFS, DRFI, and OS. Conclusion In two national randomized clinical trials using contemporary adjuvant chemotherapy, we confirm that stromal lymphocytic infiltration constitutes a robust prognostic factor in TNBCs. Studies assessing outcomes and therapeutic efficacies should consider stratification for this parameter.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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