Cyclooxygenase inhibitors use is associated with reduced risk of esophageal adenocarcinoma in patients with Barrett’s esophagus: a meta-analysis

Background: Esophageal adenocarcinoma (EAC) has high mortality and is increasing in incidence. Barrett’s esophagus (BE) increases the risk for EAC. Studies have reported inconsistent findings on the association between use of cyclooxygenase (COX) inhibitors and the risk of neoplastic progression in...

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Veröffentlicht in:British journal of cancer 2014-04, Vol.110 (9), p.2378-2388
Hauptverfasser: Zhang, S, Zhang, X-Q, Ding, X-W, Yang, R-K, Huang, S-L, Kastelein, F, Bruno, M, Yu, X-J, Zhou, D, Zou, X-P
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container_end_page 2388
container_issue 9
container_start_page 2378
container_title British journal of cancer
container_volume 110
creator Zhang, S
Zhang, X-Q
Ding, X-W
Yang, R-K
Huang, S-L
Kastelein, F
Bruno, M
Yu, X-J
Zhou, D
Zou, X-P
description Background: Esophageal adenocarcinoma (EAC) has high mortality and is increasing in incidence. Barrett’s esophagus (BE) increases the risk for EAC. Studies have reported inconsistent findings on the association between use of cyclooxygenase (COX) inhibitors and the risk of neoplastic progression in BE patients. Therefore, we performed a meta-analysis to investigate this association. Methods: A meta-analysis was undertaken among a total of 9 observational studies using fixed- and random-effects models, comprising 5446 participants; 605 had EAC or high-grade dysplasia (HGD). Results: Overall, COX inhibitors use was associated with a reduced risk of EAC/HGD among BE patients (relative risk (RR)=0.64, 95% confidence interval (CI)=0.53–0.77). Aspirin use also reduced the risk of EAC/HGD (RR=0.63, 95% CI=0.43–0.94), as well as non-aspirin COX inhibitors (RR=0.50, 95% CI=0.32–0.78). The chemopreventive effect seemed to be independent of duration response. Conclusions: Cyclooxygenase inhibitors use is associated with a reduced risk of developing EAC in patients with BE. Both low-dose aspirin and non-aspirin COX inhibitors are associated with a reduced risk of neoplasia. More well-designed randomised controlled trials are needed to increase our understanding of the chemopreventive effect of COX inhibitors.
doi_str_mv 10.1038/bjc.2014.127
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Barrett’s esophagus (BE) increases the risk for EAC. Studies have reported inconsistent findings on the association between use of cyclooxygenase (COX) inhibitors and the risk of neoplastic progression in BE patients. Therefore, we performed a meta-analysis to investigate this association. Methods: A meta-analysis was undertaken among a total of 9 observational studies using fixed- and random-effects models, comprising 5446 participants; 605 had EAC or high-grade dysplasia (HGD). Results: Overall, COX inhibitors use was associated with a reduced risk of EAC/HGD among BE patients (relative risk (RR)=0.64, 95% confidence interval (CI)=0.53–0.77). Aspirin use also reduced the risk of EAC/HGD (RR=0.63, 95% CI=0.43–0.94), as well as non-aspirin COX inhibitors (RR=0.50, 95% CI=0.32–0.78). The chemopreventive effect seemed to be independent of duration response. Conclusions: Cyclooxygenase inhibitors use is associated with a reduced risk of developing EAC in patients with BE. Both low-dose aspirin and non-aspirin COX inhibitors are associated with a reduced risk of neoplasia. More well-designed randomised controlled trials are needed to increase our understanding of the chemopreventive effect of COX inhibitors.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.2014.127</identifier><identifier>PMID: 24651385</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/699/1503/1476/1322 ; 692/699/67/1504/1477 ; 692/700/565/1436 ; Adenocarcinoma - epidemiology ; Adenocarcinoma - prevention &amp; control ; Aspirin ; Barrett Esophagus - epidemiology ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cyclooxygenase Inhibitors - administration &amp; dosage ; Drug Resistance ; Epidemiology ; Esophageal cancer ; Esophageal Neoplasms - epidemiology ; Esophageal Neoplasms - prevention &amp; control ; Esophagus ; Gastroenterology ; Gastroenterology. Liver. Pancreas. Abdomen ; Gastroesophageal reflux ; Humans ; Incidence ; Medical sciences ; Meta-analysis ; Molecular Medicine ; Mortality ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Observational studies ; Oncology ; Risk ; Tumors</subject><ispartof>British journal of cancer, 2014-04, Vol.110 (9), p.2378-2388</ispartof><rights>The Author(s) 2014</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Apr 29, 2014</rights><rights>Copyright © 2014 Cancer Research UK 2014 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-3a5205219eed74bc4b1576f5a65992726bc58392a9059aa2b5746eae6ddef64d3</citedby><cites>FETCH-LOGICAL-c480t-3a5205219eed74bc4b1576f5a65992726bc58392a9059aa2b5746eae6ddef64d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007227/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007227/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28502913$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24651385$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, S</creatorcontrib><creatorcontrib>Zhang, X-Q</creatorcontrib><creatorcontrib>Ding, X-W</creatorcontrib><creatorcontrib>Yang, R-K</creatorcontrib><creatorcontrib>Huang, S-L</creatorcontrib><creatorcontrib>Kastelein, F</creatorcontrib><creatorcontrib>Bruno, M</creatorcontrib><creatorcontrib>Yu, X-J</creatorcontrib><creatorcontrib>Zhou, D</creatorcontrib><creatorcontrib>Zou, X-P</creatorcontrib><title>Cyclooxygenase inhibitors use is associated with reduced risk of esophageal adenocarcinoma in patients with Barrett’s esophagus: a meta-analysis</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Background: Esophageal adenocarcinoma (EAC) has high mortality and is increasing in incidence. Barrett’s esophagus (BE) increases the risk for EAC. Studies have reported inconsistent findings on the association between use of cyclooxygenase (COX) inhibitors and the risk of neoplastic progression in BE patients. Therefore, we performed a meta-analysis to investigate this association. Methods: A meta-analysis was undertaken among a total of 9 observational studies using fixed- and random-effects models, comprising 5446 participants; 605 had EAC or high-grade dysplasia (HGD). Results: Overall, COX inhibitors use was associated with a reduced risk of EAC/HGD among BE patients (relative risk (RR)=0.64, 95% confidence interval (CI)=0.53–0.77). Aspirin use also reduced the risk of EAC/HGD (RR=0.63, 95% CI=0.43–0.94), as well as non-aspirin COX inhibitors (RR=0.50, 95% CI=0.32–0.78). The chemopreventive effect seemed to be independent of duration response. Conclusions: Cyclooxygenase inhibitors use is associated with a reduced risk of developing EAC in patients with BE. Both low-dose aspirin and non-aspirin COX inhibitors are associated with a reduced risk of neoplasia. More well-designed randomised controlled trials are needed to increase our understanding of the chemopreventive effect of COX inhibitors.</description><subject>692/699/1503/1476/1322</subject><subject>692/699/67/1504/1477</subject><subject>692/700/565/1436</subject><subject>Adenocarcinoma - epidemiology</subject><subject>Adenocarcinoma - prevention &amp; control</subject><subject>Aspirin</subject><subject>Barrett Esophagus - epidemiology</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cyclooxygenase Inhibitors - administration &amp; dosage</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Esophageal cancer</subject><subject>Esophageal Neoplasms - epidemiology</subject><subject>Esophageal Neoplasms - prevention &amp; control</subject><subject>Esophagus</subject><subject>Gastroenterology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gastroesophageal reflux</subject><subject>Humans</subject><subject>Incidence</subject><subject>Medical sciences</subject><subject>Meta-analysis</subject><subject>Molecular Medicine</subject><subject>Mortality</subject><subject>Multiple tumors. Solid tumors. 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Liver. Pancreas. Abdomen</topic><topic>Gastroesophageal reflux</topic><topic>Humans</topic><topic>Incidence</topic><topic>Medical sciences</topic><topic>Meta-analysis</topic><topic>Molecular Medicine</topic><topic>Mortality</topic><topic>Multiple tumors. Solid tumors. 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Barrett’s esophagus (BE) increases the risk for EAC. Studies have reported inconsistent findings on the association between use of cyclooxygenase (COX) inhibitors and the risk of neoplastic progression in BE patients. Therefore, we performed a meta-analysis to investigate this association. Methods: A meta-analysis was undertaken among a total of 9 observational studies using fixed- and random-effects models, comprising 5446 participants; 605 had EAC or high-grade dysplasia (HGD). Results: Overall, COX inhibitors use was associated with a reduced risk of EAC/HGD among BE patients (relative risk (RR)=0.64, 95% confidence interval (CI)=0.53–0.77). Aspirin use also reduced the risk of EAC/HGD (RR=0.63, 95% CI=0.43–0.94), as well as non-aspirin COX inhibitors (RR=0.50, 95% CI=0.32–0.78). The chemopreventive effect seemed to be independent of duration response. Conclusions: Cyclooxygenase inhibitors use is associated with a reduced risk of developing EAC in patients with BE. Both low-dose aspirin and non-aspirin COX inhibitors are associated with a reduced risk of neoplasia. More well-designed randomised controlled trials are needed to increase our understanding of the chemopreventive effect of COX inhibitors.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24651385</pmid><doi>10.1038/bjc.2014.127</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects 692/699/1503/1476/1322
692/699/67/1504/1477
692/700/565/1436
Adenocarcinoma - epidemiology
Adenocarcinoma - prevention & control
Aspirin
Barrett Esophagus - epidemiology
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Cancer Research
Cyclooxygenase Inhibitors - administration & dosage
Drug Resistance
Epidemiology
Esophageal cancer
Esophageal Neoplasms - epidemiology
Esophageal Neoplasms - prevention & control
Esophagus
Gastroenterology
Gastroenterology. Liver. Pancreas. Abdomen
Gastroesophageal reflux
Humans
Incidence
Medical sciences
Meta-analysis
Molecular Medicine
Mortality
Multiple tumors. Solid tumors. Tumors in childhood (general aspects)
Observational studies
Oncology
Risk
Tumors
title Cyclooxygenase inhibitors use is associated with reduced risk of esophageal adenocarcinoma in patients with Barrett’s esophagus: a meta-analysis
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