Long-term survival in HER2-positive metastatic breast cancer treated with first-line trastuzumab: results from the french real-life curie database.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 24 04 2019
accepted: 27 08 2019
pubmed: 6 9 2019
medline: 21 3 2020
entrez: 6 9 2019
Statut: ppublish

Résumé

Outcome of HER2-positive metastatic breast cancer (MBC) patients has improved since the use of trastuzumab. However, most HER2-positive MBC patients will progress within 1 year of trastuzumab-based therapy. Only limited data are available concerning long-term responders. The primary objective of this study was to compare overall survival (OS) of HER2+ MBC patients with long-term response to first-line trastuzumab with overall survival of those with non-long-term response, based on two institutional databases: the French Epidemiological Strategy and Medical Economics program and the Breast Database. Long-term responders (LTR) were defined as patients with non-progressive disease for ≥ 2 years on first-line trastuzumab. Secondary objectives included progression-free survival (PFS), and predictive factors for LTR status. From 2004 to 2014, 422 HER2-positive MBC patients received first-line trastuzumab. With a median follow-up of 48 months, median OS and PFS were 63 months (CI95%, 50-71), and 18 months (CI95%, 15-21) respectively. In 111 patients (26.3%) classified as LTR, median OS was 110 months (CI95%, 95-not reached) versus 56 months in non-LTR patients (CI95%, 47-68). In multivariate logistic regressions, the following factors were independently associated with LTR status: number of metastatic sites (≤ 2 versus > 2, p = 0.01); endocrine therapy for metastatic disease (p = 0.001) and taxane-based first-line chemotherapy (p = 0.003). Several features are associated with long-term response to trastuzumab: few metastatic sites, taxane-based chemotherapy and maintenance endocrine therapy in HR+ patients. Further studies are needed to identify patients in whom trastuzumab can be stopped after several years of sustained response.

Sections du résumé

BACKGROUND BACKGROUND
Outcome of HER2-positive metastatic breast cancer (MBC) patients has improved since the use of trastuzumab. However, most HER2-positive MBC patients will progress within 1 year of trastuzumab-based therapy. Only limited data are available concerning long-term responders.
METHODS METHODS
The primary objective of this study was to compare overall survival (OS) of HER2+ MBC patients with long-term response to first-line trastuzumab with overall survival of those with non-long-term response, based on two institutional databases: the French Epidemiological Strategy and Medical Economics program and the Breast Database. Long-term responders (LTR) were defined as patients with non-progressive disease for ≥ 2 years on first-line trastuzumab. Secondary objectives included progression-free survival (PFS), and predictive factors for LTR status.
RESULTS RESULTS
From 2004 to 2014, 422 HER2-positive MBC patients received first-line trastuzumab. With a median follow-up of 48 months, median OS and PFS were 63 months (CI95%, 50-71), and 18 months (CI95%, 15-21) respectively. In 111 patients (26.3%) classified as LTR, median OS was 110 months (CI95%, 95-not reached) versus 56 months in non-LTR patients (CI95%, 47-68). In multivariate logistic regressions, the following factors were independently associated with LTR status: number of metastatic sites (≤ 2 versus > 2, p = 0.01); endocrine therapy for metastatic disease (p = 0.001) and taxane-based first-line chemotherapy (p = 0.003).
CONCLUSION CONCLUSIONS
Several features are associated with long-term response to trastuzumab: few metastatic sites, taxane-based chemotherapy and maintenance endocrine therapy in HR+ patients. Further studies are needed to identify patients in whom trastuzumab can be stopped after several years of sustained response.

Identifiants

pubmed: 31486993
doi: 10.1007/s10549-019-05423-5
pii: 10.1007/s10549-019-05423-5
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

505-512

Auteurs

E Kaczmarek (E)

Department of Medical Oncology, Oscar Lambret Center, Lille, France. e-kaczmarek@o-lambret.fr.
Department of Biostatistics, Institut Curie, Paris, France. e-kaczmarek@o-lambret.fr.
Department of Medical Oncology, Institut Curie, Paris, France. e-kaczmarek@o-lambret.fr.
Department of Surgical Oncology, Institut Curie, Paris, France. e-kaczmarek@o-lambret.fr.
R&D, Unicancer, UCBG, Paris, France. e-kaczmarek@o-lambret.fr.

C Saint-Martin (C)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

J-Y Pierga (JY)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

E Brain (E)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

R Rouzier (R)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

A Savignoni (A)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

E Mouret-Fourme (E)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

V Dieras (V)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

I Piot (I)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

C Dubot (C)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

M Carton (M)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

F Lerebours (F)

Department of Medical Oncology, Oscar Lambret Center, Lille, France.
Department of Biostatistics, Institut Curie, Paris, France.
Department of Medical Oncology, Institut Curie, Paris, France.
Department of Surgical Oncology, Institut Curie, Paris, France.
R&D, Unicancer, UCBG, Paris, France.

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Classifications MeSH