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Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis

BACKGROUND AND AIM: A number of recent studies have been published evaluating the chemopreventive effect of aspirin against gastric cancer, and an updated meta‐analysis is required to evaluate this relationship further. This study presents a meta‐analysis of studies examining the effect of aspirin o...

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Autores principales: Niikura, Ryota, Hirata, Yoshihiro, Hayakawa, Yoku, Kawahara, Takuya, Yamada, Atsuo, Koike, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144786/
https://www.ncbi.nlm.nih.gov/pubmed/32280753
http://dx.doi.org/10.1002/jgh3.12226
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author Niikura, Ryota
Hirata, Yoshihiro
Hayakawa, Yoku
Kawahara, Takuya
Yamada, Atsuo
Koike, Kazuhiko
author_facet Niikura, Ryota
Hirata, Yoshihiro
Hayakawa, Yoku
Kawahara, Takuya
Yamada, Atsuo
Koike, Kazuhiko
author_sort Niikura, Ryota
collection PubMed
description BACKGROUND AND AIM: A number of recent studies have been published evaluating the chemopreventive effect of aspirin against gastric cancer, and an updated meta‐analysis is required to evaluate this relationship further. This study presents a meta‐analysis of studies examining the effect of aspirin on gastric cancer incidence and death. METHODS: The PUBMED and Cochrane Central Registration of Controlled Trials databases were searched for eligible studies published up to December 2018. Pooled risk ratios for gastric cancer incidence and death in aspirin users versus nonusers were determined using fixed‐ and random‐effects models. The influence of the frequency of aspirin use, duration of aspirin use, and geographic location on gastric cancer incidence was evaluated. RESULTS: The meta‐analysis comprised 33 studies with a total of 1 927 971 patients. The pooled risk ratios for gastric cancer incidence in the fixed‐ and random‐effects models were 0.890 (95% confidence interval, 0.871–0.909) and 0.826 (0.740–0.922), respectively. In Asia and North America, the maximum preventive benefit of aspirin use was observed with weekly or daily use. Aspirin use was most effective for noncardiac gastric cancer. The pooled risk ratios for gastric cancer death in the fixed‐ and random‐effects models were 0.798 (0.749–0.850) and 0.894 (0.780–1.024), respectively. Significant heterogeneity was observed among studies of gastric cancer incidence but not gastric cancer death. CONCLUSION: Aspirin use may reduce the risk of gastric cancer incidence and death; however, the relationship may be limited to a specific frequency and duration of aspirin use and geographic location.
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spelling pubmed-71447862020-04-10 Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis Niikura, Ryota Hirata, Yoshihiro Hayakawa, Yoku Kawahara, Takuya Yamada, Atsuo Koike, Kazuhiko JGH Open Original Articles BACKGROUND AND AIM: A number of recent studies have been published evaluating the chemopreventive effect of aspirin against gastric cancer, and an updated meta‐analysis is required to evaluate this relationship further. This study presents a meta‐analysis of studies examining the effect of aspirin on gastric cancer incidence and death. METHODS: The PUBMED and Cochrane Central Registration of Controlled Trials databases were searched for eligible studies published up to December 2018. Pooled risk ratios for gastric cancer incidence and death in aspirin users versus nonusers were determined using fixed‐ and random‐effects models. The influence of the frequency of aspirin use, duration of aspirin use, and geographic location on gastric cancer incidence was evaluated. RESULTS: The meta‐analysis comprised 33 studies with a total of 1 927 971 patients. The pooled risk ratios for gastric cancer incidence in the fixed‐ and random‐effects models were 0.890 (95% confidence interval, 0.871–0.909) and 0.826 (0.740–0.922), respectively. In Asia and North America, the maximum preventive benefit of aspirin use was observed with weekly or daily use. Aspirin use was most effective for noncardiac gastric cancer. The pooled risk ratios for gastric cancer death in the fixed‐ and random‐effects models were 0.798 (0.749–0.850) and 0.894 (0.780–1.024), respectively. Significant heterogeneity was observed among studies of gastric cancer incidence but not gastric cancer death. CONCLUSION: Aspirin use may reduce the risk of gastric cancer incidence and death; however, the relationship may be limited to a specific frequency and duration of aspirin use and geographic location. Wiley Publishing Asia Pty Ltd 2019-07-19 /pmc/articles/PMC7144786/ /pubmed/32280753 http://dx.doi.org/10.1002/jgh3.12226 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Niikura, Ryota
Hirata, Yoshihiro
Hayakawa, Yoku
Kawahara, Takuya
Yamada, Atsuo
Koike, Kazuhiko
Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title_full Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title_fullStr Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title_full_unstemmed Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title_short Effect of aspirin use on gastric cancer incidence and survival: A systematic review and meta‐analysis
title_sort effect of aspirin use on gastric cancer incidence and survival: a systematic review and meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144786/
https://www.ncbi.nlm.nih.gov/pubmed/32280753
http://dx.doi.org/10.1002/jgh3.12226
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