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

BACKGROUND: 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. PATIENTS AND METHODS: To investigate chemosensitivity and long-ter...

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Detalles Bibliográficos
Autores principales: Ilie, Silvia Mihaela, Briot, Nathalie, Constantin, Guillaume, Roussot, Nicolas, Ilie, Alis, Bergeron, Anthony, Arnould, Laurent, Beltjens, Françoise, Desmoulin, Isabelle, Mayeur, Didier, Kaderbhai, Courèche, Hennequin, Audrey, Jankowski, Clémentine, Padeano, Marie Martine, Costaz, Helène, Amet, Alix, Coutant, Charles, Coudert, Bruno, Bertaut, Aurélie, Ladoire, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587331/
https://www.ncbi.nlm.nih.gov/pubmed/37561255
http://dx.doi.org/10.1007/s12282-023-01490-1
Descripción
Sumario:BACKGROUND: 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. PATIENTS AND METHODS: 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. RESULTS: 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. CONCLUSIONS: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12282-023-01490-1.