The role of CDK4/6 inhibitors in older and younger patients with breast cancer: A systematic review and meta-analysis.
Breast cancer
CDK4/6 inhibitors
Elderly
Meta-analysis
Metastatic disease
Journal
Breast (Edinburgh, Scotland)
ISSN: 1532-3080
Titre abrégé: Breast
Pays: Netherlands
ID NLM: 9213011
Informations de publication
Date de publication:
Oct 2023
Oct 2023
Historique:
received:
14
04
2023
revised:
08
05
2023
accepted:
09
05
2023
medline:
15
9
2023
pubmed:
18
5
2023
entrez:
17
5
2023
Statut:
ppublish
Résumé
Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors have an extremely important impact on the treatment of hormone-sensitive breast cancer (BC) and have radically changed the first-line treatment for metastatic disease with increased rates of treatment response, overall survival (OS), and progression-free survival (PFS). We performed a pooled analysis of randomized trials to validate or refute the hypothesis that there is a significant survival benefit of adding anti-CDK4/6 inhibitors to standard endocrine therapy (ET) in older patients with advanced BC. We selected only English-language phase II/III randomized controlled trials that compared ET alone with ET with anti-CDK4/6 inhibitors in the treatment of advanced BC, with subgroups reporting the outcomes of elderly patients (usually at least 65 years). The primary endpoint was OS. The review process led to the inclusion of 12 articles and two meeting abstracts, including a total of 10 trials. The addition of CDK4/6 inhibitors to ET (letrozole or fulvestrant) significantly reduced mortality risk by 20% in younger patients (fixed-effect model; HR 0.80; 95% CI 0.72-0.9; p < 0.01) and 21% in older BC patients (HR 0.79; 95% CI 0.69-0.91; p < 0.01). No OS data were available for patients ≥70 years. This large, pooled analysis is the first to demonstrate that CDK4/6 inhibitors confer OS and PFS benefits in elderly patients (those aged ≥65 years) with advanced ER + BC and to indicate that it should be discussed with and offered to all patients after geriatric assessment and according to the toxicity profile.
Identifiants
pubmed: 37198053
pii: S0960-9776(23)00459-9
doi: 10.1016/j.breast.2023.05.002
pmc: PMC10512091
pii:
doi:
Substances chimiques
Cyclin-Dependent Kinase 4
EC 2.7.11.22
Receptor, ErbB-2
EC 2.7.10.1
Cyclin-Dependent Kinase 6
EC 2.7.11.22
Fulvestrant
22X328QOC4
Protein Kinase Inhibitors
0
Types de publication
Meta-Analysis
Systematic Review
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
138-142Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.
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