Pioglitazone and bladder cancer risk: a systematic review and meta-analysis

被引:88
|
作者
Tang, Huilin [1 ,2 ,3 ]
Shi, Weilong [3 ]
Fu, Shuangshuang [4 ]
Wang, Tiansheng [5 ]
Zhai, Suodi [3 ]
Song, Yiqing [1 ,2 ]
Han, Jiali [1 ,2 ,6 ]
机构
[1] Indiana Univ, Richard M Fairbanks Sch Publ Hlth, Dept Epidemiol, 1050 Wishard Blvd, Indianapolis, IN 46202 USA
[2] Indiana Univ, Richard M Fairbanks Sch Publ Hlth, Ctr Pharmacoepidemiol, Indianapolis, IN 46202 USA
[3] Peking Univ, Hosp 3, Dept Pharm, Beijing, Peoples R China
[4] Univ Texas Hlth Sci Ctr Houston, Sch Publ Hlth, Houston, TX 77030 USA
[5] Univ North Carolina Chapel Hill, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[6] Indiana Univ, Melvin & Bren Simon Canc Ctr, Indianapolis, IN 46202 USA
来源
CANCER MEDICINE | 2018年 / 7卷 / 04期
关键词
Bladder cancer; dose-response relationship; meta-analysis; pioglitazone; TREND ESTIMATION; THIAZOLIDINEDIONES; INSULIN; ASSOCIATION; THERAPY; MODELS; TRIAL;
D O I
10.1002/cam4.1354
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Current evidence about the association between pioglitazone and bladder cancer risk remains conflict. We aimed to assess the risk of bladder cancer associated with the use of pioglitazone and identify modifiers that affect the results. We systematically searched PubMed, Embase, and Cochrane Central Register of Controlled Trials from inception to 25 August 2016 for randomized controlled trials (RCTs) and observational studies that evaluated the association between pioglitazone and bladder cancer risk. Conventional and cumulative meta-analyses were used to calculate the odds ratio (OR) with 95% confidence interval (CI). A restricted spline regression analysis was used to examine the dose-response relationship with a generalized least-squares trend test. We included two RCTs involving 9114 patients and 20 observational studies (n = 4,846,088 individuals). An increased risk of bladder cancer in patients treated with pioglitazone versus placebo was noted from RCTs (OR, 1.84; 95%CI, 0.99 to 3.42). In observational studies, the increased risk of bladder cancer was slight but significant among ever-users of pioglitazone versus never-users (OR, 1.13; 95%CI, 1.03 to 1.25), which appeared to be both time- (P = 0.003) and dose-dependent (P = 0.05). In addition, we observed the association differed by region of studies (Europe, United States, or Asia) or source of funding (sponsored by industry or not). Current evidence suggests that pioglitazone may increase the risk of bladder cancer, possibly in a dose- and time-dependent manner. Patients with long-term and high-dose exposure to pioglitazone should be monitored regularly for signs of bladder cancer.
引用
收藏
页码:1070 / 1080
页数:11
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