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Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies
Experiments have shown that metformin can inhibit cancer cell growth, but clinical observations have been inconsistent, so we pooled the currently available data to evaluate the impact of metformin on cancer survival and progression. METHODS: PubMed, web of science, Embase, and Cochrane databases we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750609/ https://www.ncbi.nlm.nih.gov/pubmed/36626437 http://dx.doi.org/10.1097/MD.0000000000031799 |
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author | Yang, Jing Yang, Hang Cao, Ling Yin, Yuzhen Shen, Ying Zhu, Wei |
author_facet | Yang, Jing Yang, Hang Cao, Ling Yin, Yuzhen Shen, Ying Zhu, Wei |
author_sort | Yang, Jing |
collection | PubMed |
description | Experiments have shown that metformin can inhibit cancer cell growth, but clinical observations have been inconsistent, so we pooled the currently available data to evaluate the impact of metformin on cancer survival and progression. METHODS: PubMed, web of science, Embase, and Cochrane databases were searched. Pooled hazard ratios (HRs) were identified using a random-effects model to estimate the strength of the association between metformin and survival and progression in cancer patients. RESULTS: We incorporated 80 articles published from all databases which satisfied the inclusion criterion. It showed that metformin was associated with better overall survival (hazard ratio [HR] = 0. 81; 95% confidence interval [CI]: [0.77–0.85]) and cancer-specific survival (HR = 0.79; 95% CI: [0.73–0.86]), and metformin was associated with progression-free survival (HR = 0.76; 95% CI: [0.66–0.87]). In patients with diabetes mellitus, the HR of overall survival was 0.79(95% CI: [0.75–0.83]), progression-free survival was 0.72(95% CI: [0.60–0.85]), and the cancer-specific survival was 0.76(95% CI: [0.68–0.86]). It was proposed that metformin can improve the prognosis of cancer patients with diabetes mellitus. CONCLUSION: Based on cohort studies, metformin therapy has potential survival benefits for patients with malignancy, especially with the greatest benefits seen in breast cancer on overall survival, progression-free survival, and cancer-specific survival. And metformin also showed potential benefits in cancer-specific survival in colorectal and prostate cancer. |
format | Online Article Text |
id | pubmed-9750609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97506092022-12-28 Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies Yang, Jing Yang, Hang Cao, Ling Yin, Yuzhen Shen, Ying Zhu, Wei Medicine (Baltimore) 5700 Experiments have shown that metformin can inhibit cancer cell growth, but clinical observations have been inconsistent, so we pooled the currently available data to evaluate the impact of metformin on cancer survival and progression. METHODS: PubMed, web of science, Embase, and Cochrane databases were searched. Pooled hazard ratios (HRs) were identified using a random-effects model to estimate the strength of the association between metformin and survival and progression in cancer patients. RESULTS: We incorporated 80 articles published from all databases which satisfied the inclusion criterion. It showed that metformin was associated with better overall survival (hazard ratio [HR] = 0. 81; 95% confidence interval [CI]: [0.77–0.85]) and cancer-specific survival (HR = 0.79; 95% CI: [0.73–0.86]), and metformin was associated with progression-free survival (HR = 0.76; 95% CI: [0.66–0.87]). In patients with diabetes mellitus, the HR of overall survival was 0.79(95% CI: [0.75–0.83]), progression-free survival was 0.72(95% CI: [0.60–0.85]), and the cancer-specific survival was 0.76(95% CI: [0.68–0.86]). It was proposed that metformin can improve the prognosis of cancer patients with diabetes mellitus. CONCLUSION: Based on cohort studies, metformin therapy has potential survival benefits for patients with malignancy, especially with the greatest benefits seen in breast cancer on overall survival, progression-free survival, and cancer-specific survival. And metformin also showed potential benefits in cancer-specific survival in colorectal and prostate cancer. Lippincott Williams & Wilkins 2022-12-09 /pmc/articles/PMC9750609/ /pubmed/36626437 http://dx.doi.org/10.1097/MD.0000000000031799 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 5700 Yang, Jing Yang, Hang Cao, Ling Yin, Yuzhen Shen, Ying Zhu, Wei Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title | Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title_full | Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title_fullStr | Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title_full_unstemmed | Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title_short | Prognostic value of metformin in cancers: An updated meta-analysis based on 80 cohort studies |
title_sort | prognostic value of metformin in cancers: an updated meta-analysis based on 80 cohort studies |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750609/ https://www.ncbi.nlm.nih.gov/pubmed/36626437 http://dx.doi.org/10.1097/MD.0000000000031799 |
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