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Tumor-Infiltrating Lymphocytes in Patients Receiving Trastuzumab/Pertuzumab-Based Chemotherapy: A TRYPHAENA Substudy.

Authors :
Ignatiadis, Michail
Eynden, Gert Van den
Roberto, Salgado
Fornili, Marco
Bareche, Yacine
Desmedt, Christine
Rothé, Françoise
Maetens, Marion
Venet, David
Holgado, Esther
McNally, Virginia
Kiermaier, Astrid
Savage, Heidi M
Wilson, Timothy R
Cortes, Javier
Schneeweiss, Andreas
Willard-Gallo, Karen
Biganzoli, Elia
Sotiriou, Christos
Van den Eynden, Gert
Source :
JNCI: Journal of the National Cancer Institute; Jan2019, Vol. 111 Issue 1, p69-77, 9p, 4 Charts, 4 Graphs
Publication Year :
2019

Abstract

<bold>Background: </bold>There is an urgent requirement to identify biomarkers to tailor treatment in human epidermal growth factor receptor 2 (HER2)-amplified early breast cancer treated with trastuzumab/pertuzumab-based chemotherapy.<bold>Methods: </bold>Among the 225 patients randomly assigned to trastuzumab/pertuzumab concurrently or sequentially with an anthracycline-containing regimen or concurrently with an anthracycline-free regimen in the Tryphaena trial, we determined the percentage of tumor-infiltrating lymphocytes (TILs) at baseline in 213 patients, of which 126 demonstrated a pathological complete response (pCR; ypT0/is ypN0), with 28 demonstrating event-free survival (EFS) events. We investigated associations between baseline TIL percentage and either pCR or EFS after adjusting for clinicopathological characteristics using logistic and Cox regression models, respectively. To understand TIL biology, we evaluated associations between baseline TILs and baseline tumor gene expression data (800 gene set by NanoString) in a subset of 173 patients. All statistical tests were two-sided.<bold>Results: </bold>Among the patients with measurable TILs at baseline, the median level was 14.1% (interquartile range = 7.1%-32.4%). After adjusting for clinicopathological characteristics, baseline percentage TIL was not associated with pCR (adjusted odds ratio [aOR] for every 10-percentage unit increase in TILs = 1.12, 95% confidence interval [CI] = 0.95 to 1.31, P = .17). At a median follow-up of 4.7 years, for every increase in baseline TILs of 10%, there was a 25% reduction in the hazard for an EFS event (aOR = 0.75, 95% CI = 0.56 to 1.00, P = .05) after adjusting for baseline clinicopathological characteristics and pCR. Additionally, genes associated with epithelial-mesenchymal transition, angiogenesis, and T-cell inhibition such as SNAIL1, ZEB1, NOTCH3, and B7-H3 were statistically significantly inversely correlated with percentage TIL.<bold>Conclusions: </bold>Baseline TIL percentage provides independent prognostic information in patients treated with trastuzumab/pertuzumab-based neoadjuvant chemotherapy. However, further validation is required. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278874
Volume :
111
Issue :
1
Database :
Complementary Index
Journal :
JNCI: Journal of the National Cancer Institute
Publication Type :
Academic Journal
Accession number :
134187536
Full Text :
https://doi.org/10.1093/jnci/djy076