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.
Ado-Trastuzumab Emtansine
Adolescent
Adult
Antibodies, Monoclonal, Humanized
Antineoplastic Combined Chemotherapy Protocols
Breast Neoplasms
/ pathology
Capecitabine
/ therapeutic use
Female
Humans
Lapatinib
Receptor, ErbB-2
/ metabolism
Retrospective Studies
Taxoids
/ therapeutic use
Trastuzumab
/ therapeutic use
Dual HER2 blockade
Lapatinib
Metastatic breast cancer
Overall survival
Progression-free survival
T-DM1
Journal
Breast (Edinburgh, Scotland)
ISSN: 1532-3080
Titre abrégé: Breast
Pays: Netherlands
ID NLM: 9213011
Informations de publication
Date de publication:
Jun 2022
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
54-60Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.