Pathologic complete response and survival in HER2-low and HER2-zero early breast cancer treated with neoadjuvant chemotherapy

Breast Cancer - Tập 30 Số 6 - Trang 997-1007 - 2023
Ilie, Silvia Mihaela1, Briot, Nathalie2, Constantin, Guillaume2, Roussot, Nicolas1, Ilie, Alis3, Bergeron, Anthony4, Arnould, Laurent4, Beltjens, Françoise4, Desmoulin, Isabelle1, Mayeur, Didier1, Kaderbhai, Courèche1, Hennequin, Audrey1, Jankowski, Clémentine5, Padeano, Marie Martine5, Costaz, Helène5, Amet, Alix5, Coutant, Charles5,6, Coudert, Bruno1, Bertaut, Aurélie2, Ladoire, Sylvain1,3,6,7
1Department of Medical Oncology, Georges Francois Leclerc Cancer Centre, Dijon, France
2Unit of Methodology and Biostatistics, Georges Francois Leclerc Cancer Centre, Dijon, France
3Platform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France
4Department of Biology and Pathology of Tumors, Georges Francois Leclerc Cancer Centre, Dijon, France
5Department of Surgical Oncology, Georges Francois Leclerc Cancer Centre, Dijon, France
6University of Burgundy-Franche Comté, Dijon, France
7INSERM U1231, Dijon, France

Tóm tắt

Breast cancers without HER2 amplification but still expressing this membrane protein constitute a new entity called HER2-low tumors. It is important to characterize them in terms of sensitivity to treatment and prognosis. To investigate chemosensitivity and long-term prognosis of HER2-low early breast cancer (eBC), compared to HER2-0 tumors, we retrospectively retrieved clinicopathological characteristics, response to treatment, and survival data from 511 patients treated for eBC with neoadjuvant chemotherapy (NAC) in a French cancer center between 2007 and 2018. Factors associated with the achievement of pathologic complete response (pCR) and survival were studied among hormone receptor positive (HR+) and negative (HR–) eBC. A total of 280 HR+ (61% HER2-low), and 231 HR– (28% HER2-low) eBC were included. We found classical clinicopathological factors usually associated with chemosensitivity and prognosis, in both HR+ and HR– eBC. By uni- and multivariable analysis, HER2 status (low vs 0) was not independently associated with pCR, either in HR+ or HR– eBC. Relapse free (RFS) and overall survival (OS) were not significantly different between HER2-low and HER2-0 among HR+ tumors. In contrast, among HR– negative tumors, RFS and OS were slightly better in HER2-0 eBC by univariable but not by multivariable analysis. In eBC patients treated with NAC, taking into account HR expression subtype and other current clinicopathological features, HER2-low tumors did not appear to have different chemosensitivity or prognosis, compared to their HER2-0 counterparts.

Tài liệu tham khảo

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