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Outcome of Everolimus-Based Therapy in Hormone-Receptor-Positive Metastatic Breast Cancer Patients After Progression on Palbociclib

Authors :
Ajay Dhakal
Mateusz Opyrchal
Saif Soniwala
Amy P. Early
Kazuaki Takabe
Thaer Khoury
Roby Antony Thomas
Adam Brufsky
Kristopher Attwood
Matthew G. Hanna
Tracy O'Connor
Ellis G. Levine
Austin Miller
Source :
Breast Cancer: Basic and Clinical Research, Vol 14 (2020), Breast Cancer : Basic and Clinical Research
Publication Year :
2020
Publisher :
SAGE Publishing, 2020.

Abstract

Background:Despite the approval of mTOR inhibitor everolimus and CDK4/6 inhibitors in the management of hormone-receptor-positive HER2 non-amplified metastatic breast cancer (HR+ HER2-MBC), the optimal sequence of therapy is unclear. There are no clinical data on efficacy of everolimus in HR+ HER2-MBC after cancer progresses on CDK4/6 inhibitors.Objective:The objective of this study is to find the efficacy of everolimus in HR+ HER2-MBC after they progress on a CDK4/6 inhibitor palbociclib.Methods:This is a retrospective, 2-institute review of HR+ HER2-MBC from Jan 2015 to March 2018 treated with everolimus after progression on palbociclib. Primary end point was median progression-free survival (PFS), secondary end points objective response rate (ORR), clinical benefit ratio (CBR), and overall survival (OS).Results:Out of 41 women with median age 61 years (33, 87) enrolled, 66% had received adjuvant systemic therapy, 61% had visceral disease, and 95% had prior nonsteroidal aromatase inhibitors. About 83% women had 3 or more chemotherapy or hormonal therapies prior to everolimus. Kaplan-Meier estimates showed a median PFS of 4.2 months (95% confidence interval [CI]: 3.2-6.2). The median OS was 18.7 months (95% CI 9.5 to not reached). Objective response rate and CBR were both 17.1%.Conclusion:Everolimus was associated with modest PFS and ORR in HR+ HER2-MBCs postprogression on palbociclib.

Details

Language :
English
ISSN :
11782234
Volume :
14
Database :
OpenAIRE
Journal :
Breast Cancer: Basic and Clinical Research
Accession number :
edsair.doi.dedup.....c6c1ba0ca329dd603d9fdb27b76320a5