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Systematic literature review and trial-level meta-analysis of aromatase inhibitors vs tamoxifen in patients with HR+/HER2-early breast cancer
被引:0
|作者:
Janni, Wolfgang
[1
]
Untch, Michael
[2
]
Harbeck, Nadia
[3
]
Gligorov, Joseph
[4
]
Jacot, William
[5
]
Chia, Stephen
[6
]
Boileau, Jean-Francois
[7
]
Gupta, Subhajit
[8
]
Mishra, Namita
[8
]
Akdere, Murat
[9
]
Danyliv, Andriy
[9
]
Curigliano, Giuseppe
[10
,11
]
机构:
[1] Ulm Univ, Dept Gynecol & Obstet, Ulm, Germany
[2] Helios Klinikum Berlin Buch, Interdisciplinary Breast Canc Ctr, Berlin, Germany
[3] Univ Hosp Munich Ludwig Maximilian, Breast Ctr, Dept Obstet & Gynecol, Munich, Germany
[4] Sorbonne Univ, AP HP, Inst Univ Cancerol, Paris, France
[5] Montpellier Univ, Inst Canc Montpellier Val Aurelle, INSERM, U1194, Montpellier, France
[6] BC Canc Res Ctr, Vancouver, BC, Canada
[7] McGill Univ, Montreal Jewish Gen Hosp, Segal Canc Ctr, Montreal, PQ, Canada
[8] Novartis Healthcare Pvt Ltd, Hyderabad, Telangana, India
[9] Novartis Pharm AG, Basel, Switzerland
[10] European Inst Oncol, IRCCS, Milan, Italy
[11] Univ Milan, Dept Oncol & Hemato Oncol, Milan, Italy
来源:
关键词:
Meta-analysis;
HR+/HER2-early breast cancer;
Adjuvant endocrine therapy;
Tamoxifen;
Aromatase inhibitor;
D O I:
10.1016/j.breast.2025.104429
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Current standard of care for patients with HR+/HER2- early breast cancer (EBC) includes adjuvant endocrine therapy with an aromatase inhibitor (AI) or tamoxifen (TAM). We present a trial-level meta-analysis on efficacy of AI vs TAM in patients with HR+/HER2- EBC. Methods: A systematic literature review was conducted using key medical literature databases (eg, PubMed; inception to October 2023) and data from conferences (to December 2023). Phase 3 randomized controlled trials (RCTs) that had >= 80 % of patients with HR+/HER2- EBC (or available subgroup data) and reported a diseasefree survival (DFS) hazard ratio for AI vs TAM were included in the meta-analysis, regardless of menopausal status and ovarian function suppression (OFS) use. The generic invariance method was used to calculate a pooled effect estimate of DFS hazard ratios and 95 % CIs. A base-case analysis (all RCTs) and scenario analyses for NSAIonly, premenopausal, and postmenopausal RCTs were conducted. Results: Five RCTs were identified for inclusion in the meta-analysis. In the base-case analysis, DFS significantly favored AI +/- OFS vs TAM +/- OFS (pooled hazard ratio, 0.68; 95 % CI, 0.61-0.76; P < .0001). Results from scenario analyses were consistent with the base case; NSAI-only (pooled hazard ratio, 0.68; 95 % CI, 0.59-0.78; P < .0001), premenopausal (pooled hazard ratio, 0.65; 95 % CI, 0.56-0.76; P < .0001), and postmenopausal (pooled hazard ratio, 0.72; 95 % CI, 0.61-0.86; P = .001) RCTs favored AI +/- OFS over TAM +/- OFS. Conclusions: This trial-level meta-analysis demonstrated a significant DFS benefit with AI vs TAM for patients with HR+/HER2- EBC, which was more pronounced in premenopausal women.
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