Abstract

Tumor-infiltrating lymphocytes (TILs) have been associated with outcomes in HER2-positive breast cancer patients treated with neoadjuvant chemotherapy and trastuzumab. However, it remains unclear if TILs could be a prognostic and/or predictive biomarker in the context of dual HER2-targeting treatment. In this study, we evaluated the association between TILs and pathological response (pCR) and invasive-disease free survival (IDFS) in 389 patients with stage II-III HER2 positive breast cancer who received neoadjuvant anthracycline-containing or anthracycline-free chemotherapy combined with trastuzumab and pertuzumab in the TRAIN-2 trial. Although no significant association was seen between TILs and pCR, patients with TIL scores ≥60% demonstrated an excellent 3-year IDFS of 100% (95% CI 100–100), regardless of hormone receptor status, nodal stage and attainment of pCR. Additionally, in patients with hormone receptor positive disease, TILs as a continuous variable showed a trend to a positive association with pCR (adjusted Odds Ratio per 10% increase in TILs 1.15, 95% CI 0.99–1.34, p = 0.070) and IDFS (adjusted Hazard Ratio per 10% increase in TILs 0.71, 95% CI 0.50–1.01, p = 0.058). We found no interactions between TILs and anthracycline treatment. Our results suggest that high TIL scores might be able to identify stage II-III HER2-positive breast cancer patients with a favorable prognosis.

Details

Title
Tumor-infiltrating lymphocytes in HER2-positive breast cancer treated with neoadjuvant chemotherapy and dual HER2-blockade
Author
Liefaard, M. C. 1   VIAFID ORCID Logo  ; van der Voort, A. 2 ; van Seijen, M. 3 ; Thijssen, B. 4   VIAFID ORCID Logo  ; Sanders, J. 5 ; Vonk, S. 6 ; Mittempergher, L. 7   VIAFID ORCID Logo  ; Bhaskaran, R. 7 ; de Munck, L. 8   VIAFID ORCID Logo  ; van Leeuwen-Stok, A. E. 9 ; Salgado, R. 10   VIAFID ORCID Logo  ; Horlings, H. M. 5   VIAFID ORCID Logo  ; Lips, E. H. 3   VIAFID ORCID Logo  ; Sonke, G. S. 2 

 The Netherlands Cancer Institute, Division of Molecular Pathology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393); The Netherlands Cancer Institute, Department of Medical Oncology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393) 
 The Netherlands Cancer Institute, Department of Medical Oncology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393) 
 The Netherlands Cancer Institute, Division of Molecular Pathology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393) 
 Netherlands Cancer Institute, Division of Molecular Carcinogenesis, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393); Oncode Institute, Utrecht, The Netherlands (GRID:grid.499559.d) 
 The Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393) 
 The Netherlands Cancer Institute, Division of Molecular Pathology, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393); The Netherlands Cancer Institute, Core Facility Molecular Pathology & Biobanking, Amsterdam, The Netherlands (GRID:grid.430814.a) (ISNI:0000 0001 0674 1393) 
 Agendia NV, Department of Research and Development, Amsterdam, The Netherlands (GRID:grid.423768.c) (ISNI:0000 0004 0646 5300) 
 Netherlands Comprehensive Cancer Organisation (IKNL), Department of Research and Development, Utrecht, The Netherlands (GRID:grid.470266.1) (ISNI:0000 0004 0501 9982) 
 BOOG Study Center, Dutch Breast Cancer Research Group, Amsterdam, The Netherlands (GRID:grid.476173.0) 
10  GZA-ZNA Hospitals, Department of Pathology, Wilrijk, Belgium (GRID:grid.5284.b) (ISNI:0000 0001 0790 3681) 
Pages
29
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
23744677
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3041012235
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.