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Progression-Free Survival and Overall Survival of CDK 4/6 Inhibitors Plus Endocrine Therapy in Metastatic Breast Cancer: A Systematic Review and Meta-Analysis

Authors :
Michela Piezzo
Paolo Chiodini
Maria Riemma
Stefania Cocco
Roberta Caputo
Daniela Cianniello
Germira Di Gioia
Vincenzo Di Lauro
Francesca Di Rella
Giuseppina Fusco
Giovanni Iodice
Francesco Nuzzo
Carmen Pacilio
Matilde Pensabene
Michelino De Laurentiis
Source :
International Journal of Molecular Sciences, Vol 21, Iss 17, p 6400 (2020)
Publication Year :
2020
Publisher :
MDPI AG, 2020.

Abstract

The introduction of CDK4/6 inhibitors in combination with endocrine therapy (ET) represents the most relevant advance in the management of hormone receptor (HR) positive, HER2-negative metastatic breast cancer over the last few years. This meta-analysis of randomized controlled trials (RCTs) is aimed to better characterize the efficacy of CDK4/6 inhibitors in some relevant subgroups and to test heterogeneity between different compounds with a particular focus on their ability to improve overall survival (OS). Pooled estimates of hazard ratios (HRs) were computed for progression-free survival (PFS), OS, and objective response rate (ORR) analysis in predefined subgroups to better understand treatment effect concerning specific patients’ characteristics. To estimate the absolute benefit in terms of PFS, pooled survival curves were generated by pooling the data of all trials. A total of eight RCTs were included. Adding a CDK4/6 inhibitor to ET is beneficial in terms of PFS, irrespective of the presence or not of visceral metastases, the number of metastatic sites, and the length of the treatment-free interval (TFI). The addition of CDK4/6 inhibitors produces a significant OS improvement, both in aromatase inhibitor (AI)-sensitive (HR 0.75, 95% CI) and AI-resistant patients (HR 0.77, 95% CI [0.67–0.89]). Pooled data from each single drug show that palbociclib remains the only class member not showing a statistically significant HR for OS (HR 0.83, 95% CI [0.68–1.02]).

Details

Language :
English
ISSN :
14220067 and 16616596
Volume :
21
Issue :
17
Database :
Directory of Open Access Journals
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.764be9bb2233436e98198bfaa49cc350
Document Type :
article
Full Text :
https://doi.org/10.3390/ijms21176400