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

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...

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Autores principales: Tang, Huilin, Shi, Weilong, Fu, Shuangshuang, Wang, Tiansheng, Zhai, Suodi, Song, Yiqing, Han, Jiali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911601/
https://www.ncbi.nlm.nih.gov/pubmed/29476615
http://dx.doi.org/10.1002/cam4.1354
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author Tang, Huilin
Shi, Weilong
Fu, Shuangshuang
Wang, Tiansheng
Zhai, Suodi
Song, Yiqing
Han, Jiali
author_facet Tang, Huilin
Shi, Weilong
Fu, Shuangshuang
Wang, Tiansheng
Zhai, Suodi
Song, Yiqing
Han, Jiali
author_sort Tang, Huilin
collection PubMed
description 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.
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spelling pubmed-59116012018-04-30 Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis Tang, Huilin Shi, Weilong Fu, Shuangshuang Wang, Tiansheng Zhai, Suodi Song, Yiqing Han, Jiali Cancer Med Clinical Cancer Research 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. John Wiley and Sons Inc. 2018-02-24 /pmc/articles/PMC5911601/ /pubmed/29476615 http://dx.doi.org/10.1002/cam4.1354 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Tang, Huilin
Shi, Weilong
Fu, Shuangshuang
Wang, Tiansheng
Zhai, Suodi
Song, Yiqing
Han, Jiali
Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title_full Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title_fullStr Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title_full_unstemmed Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title_short Pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
title_sort pioglitazone and bladder cancer risk: a systematic review and meta‐analysis
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911601/
https://www.ncbi.nlm.nih.gov/pubmed/29476615
http://dx.doi.org/10.1002/cam4.1354
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