Efficacy of trastuzumab emtansine (T-DM1) and lapatinib after dual HER2 inhibition with trastuzumab and pertuzumab in patient with metastatic breast cancer: Retrospective data from a French multicenter real-life cohort.


Journal

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

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 05 12 2021
revised: 07 03 2022
accepted: 09 03 2022
pubmed: 18 3 2022
medline: 4 5 2022
entrez: 17 3 2022
Statut: ppublish

Résumé

Trastuzumab-emtansine (T-DM1), as well as lapatinib plus capecitabine were proven effective in two Phase III studies, following first-line trastuzumab plus a taxane. The introduction of dual HER2 blockade by trastuzumab and pertuzumab as first-line has positioned T-DM1 into second-line, and lapatinib plus capecitabine beyond, without formal evaluation of these strategies. ESME Data Platform (NCT03275311) included individual data from all patients aged ≥18 years, in whom first-line treatment for metastatic breast cancer (MBC) was initiated between January 1, 2008 and December 31, 2016 in one of the 18 French Comprehensive Cancer Centers. The efficacy of T-DM1 and lapatinib plus capecitabine combination, following double blockade associating trastuzumab and pertuzumab were evaluated in this national real-life database. Eligibility criteria were: female, MBC, HER2+ tumor, first-line taxane-based chemotherapy and dual HER2-blockage by trastuzumab plus pertuzumab. Cohort A received second-line T-DM1, and Cohort B second-line T-DM1 and third or fourth-line lapatinib plus capecitabine. Cohort A comprised 233 patients, and Cohort B 47 patients. Median progression-free survival (PFS) was 7.1 months in Cohort A and 4.6 months in Cohort B. Median overall survival were 36.7 months and 12.9 months, respectively. PFS was significantly dependent on the preceding treatment line's duration. In cohort A, HER2 expression status was a significant predictive factor of PFS. First-line trastuzumab plus pertuzumab do not markedly diminish T-DM1's efficacy in second-line. Similarly, sequential treatment with trastuzumab plus pertuzumab then T-DM1 does not noticeably modify the efficacy of lapatinib plus capecitabine.

Identifiants

pubmed: 35299035
pii: S0960-9776(22)00054-6
doi: 10.1016/j.breast.2022.03.004
pmc: PMC8927850
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Taxoids 0
Lapatinib 0VUA21238F
Capecitabine 6804DJ8Z9U
Receptor, ErbB-2 EC 2.7.10.1
pertuzumab K16AIQ8CTM
Trastuzumab P188ANX8CK
Ado-Trastuzumab Emtansine SE2KH7T06F

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

54-60

Informations de copyright

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

Auteurs

Fabien Moinard-Butot (F)

Department of Medical Oncology, Institut de Cancérologie Strasbourg - Europe (ICANS), 17 Rue Albert Calmette, BP 23025, 67033, Strasbourg, France. Electronic address: f.moinard-butot@icans.eu.

Caroline Saint-Martin (C)

Department of Biostatistics, Institut Curie, 35 Rue Dailly, 92210, Saint-Cloud, France.

Carole Pflumio (C)

Department of Medical Oncology, Institut de Cancérologie Strasbourg - Europe (ICANS), 17 Rue Albert Calmette, BP 23025, 67033, Strasbourg, France.

Matthieu Carton (M)

Department of Biostatistics, Institut Curie, 35 Rue Dailly, 92210, Saint-Cloud, France.

William Jacot (W)

Department of Medical Oncology, Institut du Cancer de Montpellier, 208 Rue des Apothicaires, 34298, Montpellier, France; Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Montpellier, France.

Paul-Henri Cottu (PH)

Department of Medical Oncology, Institut Curie, 26 Rue d'Ulm, 75005, Paris, France.

Véronique Diéras (V)

Department of Medical Oncology, Centre Eugène Marquis, Avenue de la Bataille Flandres-Dunkerque, 35000, Rennes, France.

Florence Dalenc (F)

Department of Medical Oncology, Institut Claudius Regaud - IUCT Oncopole, 1 Avenue Irène-Joliot-Curie, 31059 Toulouse, France.

Anthony Goncalves (A)

Department of Medical Oncology, Institut Paoli-Calmettes, 232 Boulevard de Sainte-Marguerite, 13009, Marseille, France.

Marc Debled (M)

Department of Medical Oncology, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France.

Anne Patsouris (A)

Department of Medical Oncology, Institut de Cancérologie de l'Ouest Nantes & Angers, 15 Rue André Boquel, 49055, Angers, France.

Marie-Ange Mouret-Reynier (MA)

Department of Medical Oncology, Centre Jean Perrin, 58 Rue Montalembert, 63011, Clermont Ferrand, France.

Laurence Vanlemmens (L)

Medical Oncology Department, Centre Oscar Lambret, 3 Rue Frédéric Combemale, 59000, Lille, France.

Marianne Leheurteur (M)

Department of Medical Oncology, Centre Henri Becquerel, Rue d'Amiens, 76000, Rouen, France.

George Emile (G)

Department of Medical Oncology, Centre François Baclesse, 3 Avenue du Général Harris, 14000, Caen, France.

Jean-Marc Ferrero (JM)

Department of Medical Oncology, Centre Antoine Lacassagne, 33 Avenue de Valambrose, 06189, Nice, France.

Isabelle Desmoulins (I)

Department of Medical Oncology, Institut de Cancérologie de Bourgogne, 21079, Dijon, France.

Lionel Uwer (L)

Medical Oncology Department, Institut de Cancérologie de Lorraine, Vandoeuvre-lès-Nancy, 6 Avenue de Bourgogne, 54519, Vandœuvre-lès-Nancy, France.

Jean-Christophe Eymard (JC)

Department of Medical Oncology, Institut de Cancérologie Jean-Godinot, 1 Rue du Général Koenig, 51100, Reims, France.

Bianca Cheaib (B)

Department of Cancer Medicine, Gustave Roussy, 114 Rue Edouard Vaillant, 94800, Villejuif, France.

Coralie Courtinard (C)

Unicancer, Data Office, 101 Rue de Tolbiac, 75654, Paris, France; Université de Bordeaux, Inserm, Bordeaux Population Health Research Center, Epicene Team, UMR 1219, Bordeaux, France.

Thomas Bachelot (T)

Department of Medical Oncology, Centre Léon Bérard, 28 Prom. Léa et Napoléon Bullukian, 69008, Lyon, France.

Michaël Chevrot (M)

Unicancer, Data Office, 101 Rue de Tolbiac, 75654, Paris, France.

Thierry Petit (T)

Department of Medical Oncology, Institut de Cancérologie Strasbourg - Europe (ICANS), 17 Rue Albert Calmette, BP 23025, 67033, Strasbourg, France.

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Classifications MeSH