Long term outcome data from the EORTC 75111-10114 ETF/BCG randomized phase II study: Pertuzumab and trastuzumab with or without metronomic chemotherapy for older patients with HER2-positive metastatic breast cancer, followed by T-DM1 after progression.


Journal

Breast (Edinburgh, Scotland)
ISSN: 1532-3080
Titre abrégé: Breast
Pays: Netherlands
ID NLM: 9213011

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 22 03 2022
revised: 27 04 2022
accepted: 13 05 2022
pubmed: 1 6 2022
medline: 29 6 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

Older patients are at higher risk of chemotherapy-induced toxicity, raising interest in less toxic anti-HER2 regimens for older persons with HER2-positive (HER2+) metastatic breast cancer (MBC). This phase II study randomized (1:1) patients with HER2+ MBC, aged 70+ or frail 60+, to first line chemotherapy with metronomic oral cyclophosphamide (M) + Trastuzumab (T) and Pertuzumab (P) or TP alone. T-DM1 was offered in case of progression. In total, 39 and 41 patients were randomized to TP and TPM arm respectively. Median follow-up is 54.0 months. 24-month PFS was 18.7% (95% CI 8.2-32.4) and 28.7% (95% CI 15.8-43.0), respectively. A total of 49 (61.3%) patients died of whom 37 (75.5%) from disease progression; number of deaths per arm was 27 (69.2%) for TP and 22 (53.7%) for TPM. There was no significant difference in OS between the two arms (median OS TP vs TPM: 32.1 vs 37.5 months, p 0.25). Among the 40 patients who have started T-DM1 after disease progression on TP/TPM, PFS rate at 6 months after start of T-DM1 was 43.6% (95% CI: 27.7-58.5) and grade 3 or higher AE occurred in 18 pts (45%). Metronomic chemotherapy-based dual blockade (TPM), followed by T-DM1 after progression, provides an active and relatively well tolerated treatment option in an older/frail HER2+ MBC population, with a median survival of over 3 years. Nevertheless, the majority of this older/frail population died from breast cancer, highlighting the need for well tolerated and efficacious treatments in these patients.

Identifiants

pubmed: 35636341
pii: S0960-9776(22)00096-0
doi: 10.1016/j.breast.2022.05.004
pmc: PMC9157551
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
BCG Vaccine 0
Receptor, ErbB-2 EC 2.7.10.1
pertuzumab K16AIQ8CTM
Trastuzumab P188ANX8CK
Ado-Trastuzumab Emtansine SE2KH7T06F

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

100-111

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Hans Wildiers (H)

Department of General Medical Oncology, University Hospitals Leuven and Department of Oncology, KU Leuven, Leuven, Belgium. Electronic address: hans.wildiers@uzleuven.be.

Thomas Meyskens (T)

European Organization for Research and Treatment of Cancer (EORTC) - Headquarters, Brussels, Belgium.

Sandrine Marréaud (S)

European Organization for Research and Treatment of Cancer (EORTC) - Headquarters, Brussels, Belgium.

Lissandra Dal Lago (LD)

Department of Medicine, Institut Jules Bordet, Brussels, Belgium.

Peter Vuylsteke (P)

CHU UCL Namur Sainte Elisabeth, UCLouvain, Namur, Belgium.

Giuseppe Curigliano (G)

Division of Early Drug Development, Istituto Europeo di Oncologia, IRCCS, Italy; University of Milano, Milan, Italy.

Simon Waters (S)

Velindre Cancer Centre, Cardiff, UK.

Barbara Brouwers (B)

Department of Medical Oncology, AZ Sint-Jan Hospital, Brugge, Belgium.

Bart Meulemans (B)

European Organization for Research and Treatment of Cancer (EORTC) - Headquarters, Brussels, Belgium.

Berta Sousa (B)

Breast Unit, Champalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal.

Coralie Poncet (C)

European Organization for Research and Treatment of Cancer (EORTC) - Headquarters, Brussels, Belgium.

Etienne Brain (E)

Department of Medical Oncology, Institut Curie - Hôpital René Huguenin, Saint-Cloud, France.

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Classifications MeSH