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绝经后HR阳性乳腺癌新辅助内分泌治疗疗效的网状Meta分析

Network Meta-Analysis of the Effectiveness of Neoadjuvant Endocrine Therapy for Postmenopausal, HR-Positive Breast Cancer.

作者信息

Wang Wei, Liu Chenghao, Zhou Wenbin, Xia Tiansong, Xie Hui, Wang Shui

机构信息

Department of Breast Surgery, The First Affiliated Hospital with Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, China.

出版信息

Sci Rep. 2016 May 13;6:25615. doi: 10.1038/srep25615.

Abstract

In clinical practice, it is necessary to define an optimal choice from many different therapeutic regimens. This study aimed to assess the efficacy and safety of neoadjuvant endocrine therapy (NET) for breast cancer patients. Randomized clinical trials were included. Nine studies comprising 2133 patients were included in the final analysis. Network meta-analysis showed that everolimus plus letrozole was more easily accepted by patients than exemestane (≥20wks) (odds ratio (OR): 856697.02, 95% confidence intervals (95%CI): 1.88 to 87242934...); exemestane (≥20wks) had worse acceptability than letrozole (OR: 0.00, 95%CI: 0.00 to 0.98). Letrozole produced a better clinical objective response (COR) than tamoxifen (OR: 1.99, 95%CI: 1.04 to 3.80). The incidence of fatigue between the anastrozole plus gefitinib group and the everolimus plus letrozole group was significantly different (OR: 0.08, 95%CI: 0.01 to 0.83). The exemestane (<20wks) plus celecoxib group had fewer hot flushes than others. Ranking showed the everolimus plus letrozole was most likely rank first in comparisons of COR and acceptability, and had a 64% possibility to rank first after stochastic multi-criteria acceptability analysis. In conclusion, our study showed that letrozole plus everolimus is the most effective treatment for postmenopausal, hormone receptor-positive breast cancer in the neoadjuvant setting.

摘要

在临床实践中,有必要从众多不同的治疗方案中确定最佳选择。本研究旨在评估新辅助内分泌治疗(NET)对乳腺癌患者的疗效和安全性。纳入了随机临床试验。最终分析纳入了9项研究,共2133例患者。网状Meta分析显示,依维莫司联合来曲唑比依西美坦(≥20周)更容易被患者接受(优势比(OR):856697.02,95%置信区间(95%CI):1.88至87242934...);依西美坦(≥20周)的可接受性比来曲唑差(OR:0.00,95%CI:0.00至0.98)。来曲唑产生的临床客观缓解(COR)优于他莫昔芬(OR:1.99,95%CI:1.04至3.80)。阿那曲唑联合吉非替尼组和依维莫司联合来曲唑组之间疲劳发生率有显著差异(OR:0.08,95%CI:0.01至0.83)。依西美坦(<20周)联合塞来昔布组潮热比其他组少。排名显示,依维莫司联合来曲唑在COR和可接受性比较中最有可能排名第一,在随机多标准可接受性分析后有64%的可能性排名第一。总之,我们的研究表明,来曲唑联合依维莫司是新辅助治疗绝经后激素受体阳性乳腺癌最有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a795/4865840/c13597d307e0/srep25615-f1.jpg

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