Gastroesophageal reflux disease, use of H2 receptor antagonists, and risk of esophageal and gastric cancer

被引:158
作者
Farrow, DC
Vaughan, TL
Sweeney, C
Gammon, MD
Chow, WH
Risch, HA
Stanford, JL
Hansten, PD
Mayne, ST
Schoenberg, JB
Rotterdam, H
Ahsan, H
West, AB
Dubrow, R
Fraumeni, JF
Blot, WJ
机构
[1] Univ Washington, Fred Hutchinson Canc Res Ctr, Program Epidemiol, Seattle, WA 98109 USA
[2] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA 98109 USA
[3] Columbia Univ, Joseph L Mailman Sch Publ Hlth, Div Epidemiol, New York, NY USA
[4] NCI, Div Canc Epidemiol & Genet, Bethesda, MD USA
[5] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06510 USA
[6] Univ Washington, Dept Pharm, Seattle, WA 98195 USA
[7] New Jersey Dept Hlth & Senior Serv, Off Canc Epidemiol, Trenton, NJ USA
[8] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY USA
[9] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[10] Int Epidemiol Inst, Rockville, MD USA
关键词
esophageal neoplasms; gastric neoplasms; gastroesophageal reflux disease; H-2 receptor antagonists;
D O I
10.1023/A:1008913828105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The incidence of esophageal adenocarcinoma has risen rapidly in the past two decades, for unknown reasons. The goal of this analysis was to determine whether gastroesophageal reflux disease (GERD) or the medications used to treat it are associated with an increased risk of esophageal or gastric cancer, using data from a large population-based case-control study. Methods: Cases were aged 30-79 years, newly diagnosed with esophageal adenocarcinoma (n = 293), esophageal squamous cell carcinoma (n = 221), gastric cardia adenocarcinoma (n = 261), or non-cardia gastric adenocarcinoma (n = 368) in three areas with population-based tumor registries. Controls (n = 695) were chosen by random digit dialing and from Health Care Financing Administration rosters. Data were collected using an in-person structured interview. Results: History of gastric ulcer was associated with an increased risk of non-cardia gastric adenocarcinoma (OR 2.1, 95% CI 1.4-3.2). Risk of esophageal adenocarcinoma increased with frequency of GERD symptoms; the odds ratio in those reporting daily symptoms was 5.5 (95% CI 3.2-9.3). Ever having used H-2 blockers was unassociated with esophageal adenocarcinoma risk (OR 0.9, 95% CI 0.5-1.5). The odds ratio was 1.3 (95% CI 0.6-2.8) in long-term (4 or more years) users, but increased to 2.1 (95% CI 0.8-5.6) when use in the 5 years prior to the interview was disregarded. Risk was also modestly increased among users of antacids. Neither GERD symptoms nor use of H-2 blockers or antacids was associated with risk of the other three tumor types. Conclusions: Individuals with long-standing GERD are at increased risk of esophageal adenocarcinoma, whether or not the symptoms are treated with H-2 blockers or antacids.
引用
收藏
页码:231 / 238
页数:8
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