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The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis

In this work, we aim to further analyze the association of statins use with biochemical recurrence (BCR) of prostate cancer (PCa) and PCa-specific mortality after definitive therapy. A systematic literature search of PubMed, MEDLINE, and EMBASE through Jul 2015 was conducted. Pooled Hazard ratio (HR...

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Autores principales: Tan, Ping, Wei, Shiyou, Yang, Lu, Tang, Zhuang, Cao, Dehong, Liu, Liangren, Lei, Junhao, Fan, Yu, Gao, Liang, Wei, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935858/
https://www.ncbi.nlm.nih.gov/pubmed/27384548
http://dx.doi.org/10.1038/srep29106
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author Tan, Ping
Wei, Shiyou
Yang, Lu
Tang, Zhuang
Cao, Dehong
Liu, Liangren
Lei, Junhao
Fan, Yu
Gao, Liang
Wei, Qiang
author_facet Tan, Ping
Wei, Shiyou
Yang, Lu
Tang, Zhuang
Cao, Dehong
Liu, Liangren
Lei, Junhao
Fan, Yu
Gao, Liang
Wei, Qiang
author_sort Tan, Ping
collection PubMed
description In this work, we aim to further analyze the association of statins use with biochemical recurrence (BCR) of prostate cancer (PCa) and PCa-specific mortality after definitive therapy. A systematic literature search of PubMed, MEDLINE, and EMBASE through Jul 2015 was conducted. Pooled Hazard ratio (HR) estimates with corresponding 95% confidence intervals (CIs) were calculated using random-effects model. STATA version 10 (Stata corporation, college station, TX) was employed to conduct all statistical analyses. A total of 22 and 8 studies contributed to the biochemical recurrence analysis and PCa-specific mortality, respectively. 13 trials were included for BCR-free survival analysis. The combined result showed statins users had lowered 12% BCR risk of PCa compared with non-users (HR = 0.88, 95%CI: 0.765–0.998) (p < 0.05). The association was null among the men who underwent radical prostatectomy as primary therapy (HR = 0.96, 95%CI: 0.83–1.09), while the improved outcomes had be seen among patients who received radiation therapy (HR = 0.67, 95%CI: 0.48–0.86). After excluding the patients undergoing ADT, participants did not benefit from statins use (HR = 0.94, 95%CI: 0.77–1.11). Meanwhile, long-term statins using did not alter recurrence risk. A lower risk of prostate cancer-specific mortality was observed among statins users (HR = 0.68, 95%CI: 0.56–0.80). There was a plausible trend towards increasing the BCR-free survival rate among statins users.
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spelling pubmed-49358582016-07-08 The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis Tan, Ping Wei, Shiyou Yang, Lu Tang, Zhuang Cao, Dehong Liu, Liangren Lei, Junhao Fan, Yu Gao, Liang Wei, Qiang Sci Rep Article In this work, we aim to further analyze the association of statins use with biochemical recurrence (BCR) of prostate cancer (PCa) and PCa-specific mortality after definitive therapy. A systematic literature search of PubMed, MEDLINE, and EMBASE through Jul 2015 was conducted. Pooled Hazard ratio (HR) estimates with corresponding 95% confidence intervals (CIs) were calculated using random-effects model. STATA version 10 (Stata corporation, college station, TX) was employed to conduct all statistical analyses. A total of 22 and 8 studies contributed to the biochemical recurrence analysis and PCa-specific mortality, respectively. 13 trials were included for BCR-free survival analysis. The combined result showed statins users had lowered 12% BCR risk of PCa compared with non-users (HR = 0.88, 95%CI: 0.765–0.998) (p < 0.05). The association was null among the men who underwent radical prostatectomy as primary therapy (HR = 0.96, 95%CI: 0.83–1.09), while the improved outcomes had be seen among patients who received radiation therapy (HR = 0.67, 95%CI: 0.48–0.86). After excluding the patients undergoing ADT, participants did not benefit from statins use (HR = 0.94, 95%CI: 0.77–1.11). Meanwhile, long-term statins using did not alter recurrence risk. A lower risk of prostate cancer-specific mortality was observed among statins users (HR = 0.68, 95%CI: 0.56–0.80). There was a plausible trend towards increasing the BCR-free survival rate among statins users. Nature Publishing Group 2016-07-07 /pmc/articles/PMC4935858/ /pubmed/27384548 http://dx.doi.org/10.1038/srep29106 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tan, Ping
Wei, Shiyou
Yang, Lu
Tang, Zhuang
Cao, Dehong
Liu, Liangren
Lei, Junhao
Fan, Yu
Gao, Liang
Wei, Qiang
The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title_full The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title_fullStr The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title_full_unstemmed The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title_short The effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
title_sort effect of statins on prostate cancer recurrence and mortality after definitive therapy: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935858/
https://www.ncbi.nlm.nih.gov/pubmed/27384548
http://dx.doi.org/10.1038/srep29106
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