Use of aspirin and other nonsteroidal anti-inflammatory drugs and risk of esophageal and gastric cancer

被引:0
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作者
Farrow, DC
Vaughan, TL
Hansten, PD
Stanford, JL
Risch, HA
Gammon, MD
Chow, WH
Dubrow, R
Ahsan, H
Mayne, ST
Schoenberg, JB
West, AB
Rotterdam, H
Fraumeni, JF
Blot, WJ
机构
[1] Fred Hutchinson Canc Res Ctr, Program Epidemiol, Seattle, WA 98104 USA
[2] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pharm, Seattle, WA 98195 USA
[4] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[6] Columbia Sch Publ Hlth, Div Epidemiol, New York, NY 10032 USA
[7] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20852 USA
[8] New Jersey Dept Hlth & Senior Serv, Off Canc Epidemiol, Trenton, NJ 08625 USA
[9] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[10] Int Epidemiol Inst, Rockville, MD 20850 USA
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Regular users of aspirin and other nonsteroidal antiinflammatory drugs (NSAIDs) are at reduced risk of colon cancer, but the evidence for protective effects of NSAIDs elsewhere in the digestive tract is scant. We investigated the association between the use of NSAIDs and risk of esophageal and gastric cancer, using data from a large population-based, case-control study. Cases were individuals, ages 30-79 years, diagnosed with esophageal adenocarcinoma (n = 293), esophageal squamous cell carcinoma (n = 221), gastric cardia adenocarcinoma (n = 261), or noncardia gastric adenocarcinoma (n = 368) in three areas with population-based tumor registries. Controls (n = 695) were selected by random digit dialing and through the rosters of the Health Care Financing Administration. After controlling for the major risk factors, we found that current users of aspirin were at decreased risk of esophageal adenocarcinoma [odds ratio (OR), 0.37; 95% confidence interval (CI), 0.24-0.58], esophageal squamous cell carcinoma (OR, 0.49; 95% CI, 0.28-0.87), and noncardia gastric adenocarcinoma (OR, 0.46; 95% CI, 0.31-0.68), but not of gastric cardia adenocarcinoma (OR, 0.80; 95% CI, 0.54-1.19), when compared to never users. Risk was similarly reduced among current users of nonaspirin NSAIDs. The associations with current NSAID use persisted when we excluded use within 2 or 5 years of reference date, which might have been affected by preclinical disease in cases, and when we restricted analyses to subjects reporting no history of chronic gastrointestinal symptoms. Our findings add to the growing evidence that the risk of cancers of the esophagus and stomach is reduced in users of NSAIDs, although whether the association is causal in nature is not clear.
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页码:97 / 102
页数:6
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