Liu Yupeng, Zhang Xiaosan, Sun Hongru, Zhao Shu, Zhang Yuxue, Li Dapeng, Zhang Qingyuan, Zhao Yashuang
Department of Preventive Medicine, School of Public Health and Management, Wenzhou Medical University, Wenzhou 325035, People's Republic of China.
Department of Epidemiology, Public Health School of Harbin Medical University, Harbin 150081, People's Republic of China.
Clin Epidemiol. 2019 Jul 18;11:593-603. doi: 10.2147/CLEP.S194056. eCollection 2019.
Prevention of primary breast cancer (BCa) in women is of great public health importance. The existing results from observational epidemiologic studies focused on the association between bisphosphonates and primary BCa risk have been inconsistent.
To update this systematic review and meta-analysis to assess the effect of bisphosphonates on primary BCa risk.
We comprehensively searched MEDLINE, EMBASE, Cochrane libraries, ProQuest, and Web of Science through June 25, 2018 for relevant studies.
Epidemiological studies that assessed the effect of bisphosphonates on the risk of primary BCa in women.
We reported this meta-analysis according to the PRISMA guidelines. Available multivariable-adjusted effect estimates and corresponding 95% CIs were pooled with a random-effects model.
The prespecified main outcome was the risk of primary BCa.
In total, five cohort studies involving 657,558 women and 12,991 primary BCa patients, three population-based case-control studies involving 54,701 primary BCa cases and 237,962 healthy controls and two randomized controlled trials (RCTs) involving 13,774 women and 165 primary BCa patients were included in this meta-analysis. Bisphosphonates were associated with a 12% decreased risk of primary BCa (RR, 0.88; 95% CI, 0.83-0.94). However, when we analyzed study designs separately, the pooled results from observational studies were inconsistent with that from RCTs. The observed association of primary BCa risk with long-term use (≥1 year) of bisphosphonates seemed to be more robust and stronger than that of short-term use (<1 year) (RR, 0.75; 95% CI, 0.66-0.84; and 0.90; 95% CI, 0.84-0.97; respectively).
This meta-analysis adds to the body of evidence for an association between bisphosphonates and a significantly decreased risk of primary BCa. However, future large-scale RCTs are required to validate this concern.
预防女性原发性乳腺癌对公共卫生具有重大意义。观察性流行病学研究关于双膦酸盐与原发性乳腺癌风险之间关联的现有结果并不一致。
更新此系统评价和荟萃分析,以评估双膦酸盐对原发性乳腺癌风险的影响。
我们全面检索了截至2018年6月25日的MEDLINE、EMBASE、Cochrane图书馆、ProQuest和科学网,以查找相关研究。
评估双膦酸盐对女性原发性乳腺癌风险影响的流行病学研究。
我们根据PRISMA指南报告了此荟萃分析。可用的多变量调整效应估计值和相应的95%置信区间采用随机效应模型进行汇总。
预先设定的主要结局是原发性乳腺癌的风险。
本荟萃分析共纳入五项队列研究,涉及657,558名女性和12,991例原发性乳腺癌患者;三项基于人群的病例对照研究,涉及54,701例原发性乳腺癌病例和237,962名健康对照;以及两项随机对照试验,涉及13,774名女性和165例原发性乳腺癌患者。双膦酸盐与原发性乳腺癌风险降低12%相关(风险比,0.88;95%置信区间,0.83 - 0.94)。然而,当我们分别分析研究设计时,观察性研究的汇总结果与随机对照试验的结果不一致。原发性乳腺癌风险与长期使用(≥1年)双膦酸盐的观察到的关联似乎比短期使用(<1年)更强且更稳健(风险比分别为0.75;95%置信区间,0.66 - 0.84;以及0.90;95%置信区间,0.84 - 0.97)。
此荟萃分析为双膦酸盐与原发性乳腺癌风险显著降低之间的关联增添了证据。然而,未来需要大规模随机对照试验来验证这一问题。