Back to Search Start Over

Efficacy and safety of trastuzumab emtansine in older patients with HER2-positive advanced breast cancer: a real-world study

Authors :
Cil, Ibrahim
Kucukarda, Ahmet
Atcı, Muhammed Mustafa
Secmeler, Saban
Paksoy, Nail
Ferhatoglu, Ferhat
Ak, Naziye
Ayhan, Murat
Tataroglu Ozyukseler, Deniz
Onder, Arif Hakan
Avci, Okan
Oyman, Abdilkerim
Okten, Ilker Nihat
Gulturk, Ilkay
Akagunduz, Baran
Basoglu, Tugba
Cakir, Emre
Hacibekiroglu, Ilhan
Ozcelik, Melike
Aydiner, Adnan
Source :
Tumori Journal; February 2022, Vol. 108 Issue: 1 p19-25, 7p
Publication Year :
2022

Abstract

Introduction: Ado-trastuzumab emtansine (T-DM1) is an antibody–drug conjugate and its survival advantage has been shown in advanced human epidermal growth factor receptor 2 (HER2)–positive breast cancer. However, clinical trials underrepresent patients ⩾65 years of age, leading to a lack of information in this population. We analyzed the real-world outcomes of older women who were treated with T-DM1 therapy.Methods: We performed a multicenter, observational, retrospective analysis of patients aged ⩾65 years treated with T-DM1. A total of 93 patients from 10 cancer centers were involved in the study. Our goal was to determine the survival, response rates, and toxicity profile in T-DM1–treated patients, as well as the factors that influence survival.Results: Median follow-up was 12.2 months. Objective response rate was 29%. Median progression-free survival (PFS) and overall survival (OS) were 8.47 and 15.0 months, respectively. In multivariate analysis, Eastern Cooperative Oncology Group Performance Score 2 was found to be an independent prognostic factor for worse PFS (hazard ratio [HR] 1.81, p= 0.032) and OS (HR 2.33, p= 0.006). Any adverse event (AE) was seen in 92.5% of patients; grade 3 or 4 AEs were seen in 30.1%. Dose reduction or treatment discontinuation rates were 11.8% and 6.5%, respectively.Conclusion: The efficacy of T-DM1 was acceptable and it was generally well-tolerated among older patients with advanced HER2-positive breast cancer.

Details

Language :
English
ISSN :
03008916 and 20382529
Volume :
108
Issue :
1
Database :
Supplemental Index
Journal :
Tumori Journal
Publication Type :
Periodical
Accession number :
ejs58899827
Full Text :
https://doi.org/10.1177/03008916211037739