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Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis
Previous studies investigating the association between statin use and survival outcomes in gynecologic cancers have yielded controversial results. We conducted a systematic review and meta-analysis to evaluate the association based on available evidence. We searched the databases of the Cochrane Cen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522329/ https://www.ncbi.nlm.nih.gov/pubmed/28489569 http://dx.doi.org/10.18632/oncotarget.17242 |
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author | Xie, Weimin Ning, Li Huang, Yuenan Liu, Yan Zhang, Wen Hu, Yingchao Lang, Jinghe Yang, Jiaxin |
author_facet | Xie, Weimin Ning, Li Huang, Yuenan Liu, Yan Zhang, Wen Hu, Yingchao Lang, Jinghe Yang, Jiaxin |
author_sort | Xie, Weimin |
collection | PubMed |
description | Previous studies investigating the association between statin use and survival outcomes in gynecologic cancers have yielded controversial results. We conducted a systematic review and meta-analysis to evaluate the association based on available evidence. We searched the databases of the Cochrane Central Register of Controlled Trials (CENTRAL), Embase, and PubMed from inception to January 2017. Studies that evaluated the association between statin use and survival outcomes in gynecologic cancers were included. Pooled hazard ratios (HRs) for overall survival, disease-specific survival and progression-free survival were calculated using a fixed-effects model. A total of 11 studies involving more than 6,920 patients with endocrine-related gynecologic cancers were identified. In a meta-analysis of 7 studies involving 5,449 patients with endocrine-related gynecologic cancers, statin use was linked to improved overall survival (HR, 0.71; 95% confidence interval [CI], 0.63 to 0.80) without significant heterogeneity (I(2) = 33.3%). Statin users also had improved disease-specific survival (3 studies, HR, 0.72; 95% CI, 0.58 to 0.90, I(2) = 35.1%) and progression-free survival (3 studies, HR, 0.68; 95% CI, 0.49 to 0.93, I(2) = 33.6%) in endocrine-related gynecologic cancers. Our findings support that statin use has potential survival benefits for patients with endocrine-related gynecologic cancers. Further large-scale prospective studies are required to validate our findings. |
format | Online Article Text |
id | pubmed-5522329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55223292017-08-21 Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis Xie, Weimin Ning, Li Huang, Yuenan Liu, Yan Zhang, Wen Hu, Yingchao Lang, Jinghe Yang, Jiaxin Oncotarget Meta-Analysis Previous studies investigating the association between statin use and survival outcomes in gynecologic cancers have yielded controversial results. We conducted a systematic review and meta-analysis to evaluate the association based on available evidence. We searched the databases of the Cochrane Central Register of Controlled Trials (CENTRAL), Embase, and PubMed from inception to January 2017. Studies that evaluated the association between statin use and survival outcomes in gynecologic cancers were included. Pooled hazard ratios (HRs) for overall survival, disease-specific survival and progression-free survival were calculated using a fixed-effects model. A total of 11 studies involving more than 6,920 patients with endocrine-related gynecologic cancers were identified. In a meta-analysis of 7 studies involving 5,449 patients with endocrine-related gynecologic cancers, statin use was linked to improved overall survival (HR, 0.71; 95% confidence interval [CI], 0.63 to 0.80) without significant heterogeneity (I(2) = 33.3%). Statin users also had improved disease-specific survival (3 studies, HR, 0.72; 95% CI, 0.58 to 0.90, I(2) = 35.1%) and progression-free survival (3 studies, HR, 0.68; 95% CI, 0.49 to 0.93, I(2) = 33.6%) in endocrine-related gynecologic cancers. Our findings support that statin use has potential survival benefits for patients with endocrine-related gynecologic cancers. Further large-scale prospective studies are required to validate our findings. Impact Journals LLC 2017-04-19 /pmc/articles/PMC5522329/ /pubmed/28489569 http://dx.doi.org/10.18632/oncotarget.17242 Text en Copyright: © 2017 Xie et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Xie, Weimin Ning, Li Huang, Yuenan Liu, Yan Zhang, Wen Hu, Yingchao Lang, Jinghe Yang, Jiaxin Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title | Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title_full | Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title_fullStr | Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title_full_unstemmed | Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title_short | Statin use and survival outcomes in endocrine-related gynecologic cancers: A systematic review and meta-analysis |
title_sort | statin use and survival outcomes in endocrine-related gynecologic cancers: a systematic review and meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522329/ https://www.ncbi.nlm.nih.gov/pubmed/28489569 http://dx.doi.org/10.18632/oncotarget.17242 |
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