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Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer
BACKGROUND: For gynecological cancer patients, the beneficial effect of metformin use remains controversial due to inconsistent results of published articles. By conducting a meta-analysis, we aimed to evaluate the effect of metformin in reducing the risk and improving the survival of gynecological...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309370/ https://www.ncbi.nlm.nih.gov/pubmed/35898873 http://dx.doi.org/10.3389/fonc.2022.942380 |
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author | Yao, Kui Zheng, Heng Li, Tao |
author_facet | Yao, Kui Zheng, Heng Li, Tao |
author_sort | Yao, Kui |
collection | PubMed |
description | BACKGROUND: For gynecological cancer patients, the beneficial effect of metformin use remains controversial due to inconsistent results of published articles. By conducting a meta-analysis, we aimed to evaluate the effect of metformin in reducing the risk and improving the survival of gynecological cancer among women with diabetes mellitus (DM). METHODS: Articles exploring association between metformin use and the risk, as well as prognosis of gynecologic cancer in DM, were searched in the databases: PubMed, Web of Science, SCOPUS, EMBASE, EBSCO, and PROQUEST. Articles were published before May 2022. All the studies were conducted using STATA 12.0 software. RESULTS: The meta-analysis showed no significant association between metformin use and risk of gynecologic cancer in DM with a random effects model [odds ratio (ORs)/relative risk (RR) = 0.91, 95% confidence intervals (CI) 0.77 to 1.08, I(2) = 84.2%, p < 0.001]. Metformin use was associated with reduced overall survival (OS) and progression-free survival (PFS) of gynecologic cancer in DM with random effects models [OS: hazard ratio (HR) = 0.60, 95% CI 0.49–0.74, I(2) = 55.2%, p = 0.002; PFS: HR = 0.55, 95% CI 0.33–0.91, I(2) = 69.1%, p = 0.006], whereas no significant association was showed between metformin use and recurrence-free survival (RFS), as well as cancer-specific survival (CSS) of gynecologic cancer in DM with random effects models (RFS: HR = 0.60, 95% CI 0.30–1.18, I(2) = 73.7%, p = 0.010; CSS: HR = 0.78, 95% CI 0.43–1.41, I(2) = 72.4%, p = 0.013). CONCLUSIONS: In conclusion, this meta-analysis indicated that metformin may be a useful adjuvant agent for gynecological cancer with DM, especially for patients with ovarian cancer and endometrial cancer. |
format | Online Article Text |
id | pubmed-9309370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93093702022-07-26 Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer Yao, Kui Zheng, Heng Li, Tao Front Oncol Oncology BACKGROUND: For gynecological cancer patients, the beneficial effect of metformin use remains controversial due to inconsistent results of published articles. By conducting a meta-analysis, we aimed to evaluate the effect of metformin in reducing the risk and improving the survival of gynecological cancer among women with diabetes mellitus (DM). METHODS: Articles exploring association between metformin use and the risk, as well as prognosis of gynecologic cancer in DM, were searched in the databases: PubMed, Web of Science, SCOPUS, EMBASE, EBSCO, and PROQUEST. Articles were published before May 2022. All the studies were conducted using STATA 12.0 software. RESULTS: The meta-analysis showed no significant association between metformin use and risk of gynecologic cancer in DM with a random effects model [odds ratio (ORs)/relative risk (RR) = 0.91, 95% confidence intervals (CI) 0.77 to 1.08, I(2) = 84.2%, p < 0.001]. Metformin use was associated with reduced overall survival (OS) and progression-free survival (PFS) of gynecologic cancer in DM with random effects models [OS: hazard ratio (HR) = 0.60, 95% CI 0.49–0.74, I(2) = 55.2%, p = 0.002; PFS: HR = 0.55, 95% CI 0.33–0.91, I(2) = 69.1%, p = 0.006], whereas no significant association was showed between metformin use and recurrence-free survival (RFS), as well as cancer-specific survival (CSS) of gynecologic cancer in DM with random effects models (RFS: HR = 0.60, 95% CI 0.30–1.18, I(2) = 73.7%, p = 0.010; CSS: HR = 0.78, 95% CI 0.43–1.41, I(2) = 72.4%, p = 0.013). CONCLUSIONS: In conclusion, this meta-analysis indicated that metformin may be a useful adjuvant agent for gynecological cancer with DM, especially for patients with ovarian cancer and endometrial cancer. Frontiers Media S.A. 2022-07-11 /pmc/articles/PMC9309370/ /pubmed/35898873 http://dx.doi.org/10.3389/fonc.2022.942380 Text en Copyright © 2022 Yao, Zheng and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yao, Kui Zheng, Heng Li, Tao Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title | Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title_full | Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title_fullStr | Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title_full_unstemmed | Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title_short | Association Between Metformin Use and the Risk, Prognosis of Gynecologic Cancer |
title_sort | association between metformin use and the risk, prognosis of gynecologic cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309370/ https://www.ncbi.nlm.nih.gov/pubmed/35898873 http://dx.doi.org/10.3389/fonc.2022.942380 |
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