Efficacy and Safety of Trastuzumab Emtansine in Her2 Positive Metastatic Breast Cancer: Real-World Experience.
Ado-Trastuzumab Emtansine
/ administration & dosage
Adult
Aged
Aged, 80 and over
Antineoplastic Agents, Immunological
/ administration & dosage
Breast Neoplasms
/ drug therapy
Female
Humans
Middle Aged
Neoplasm Metastasis
Receptor, ErbB-2
/ genetics
Retrospective Studies
Survival Analysis
Treatment Outcome
Turkey
Metastatic breast cancer
T-DM1
efficacy
real-world experience
toxicity
Journal
Cancer investigation
ISSN: 1532-4192
Titre abrégé: Cancer Invest
Pays: England
ID NLM: 8307154
Informations de publication
Date de publication:
Historique:
pubmed:
21
5
2021
medline:
23
7
2021
entrez:
20
5
2021
Statut:
ppublish
Résumé
The aim of this study is to evaluate the efficacy and toxicity of trastuzumab emtansine (T-DM1) in cases with metastatic breast cancer (mBC) in different lines of treatment. Retrospective analysis of T-DM1 results of human epidermal growth factor receptor 2 (Her2) positive 414 cases with mBC from 31 centers in Turkey. Except 2, all of the cases were female with a median age of 47. T-DM1 had been used as second-line therapy in 37.7% of the cases and the median number of T-DM1 cycles was 9. Progression-free survival (PFS) and overall survival (OS) times were different according to the line of treatment. The median OS was found as 43, 41, 46, 23 and 17 months for 1st, 2nd, 3rd, 4th and 5th line, respectively ( The best of our knowledge this is the largest real-life experience about the safety and efficacy of T-DM1 use in cases with mBC after progression of Her2 targeted treatment. This study suggests and supports that T-DM1 is more effective in earlier lines of treatment and is a reliable option for mBC.
Identifiants
pubmed: 34014777
doi: 10.1080/07357907.2021.1933011
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
Ado-Trastuzumab Emtansine
SE2KH7T06F
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM