Cancer Epidemiology and Health Services Research Group, Centre for Public Health, Queen's University Belfast, Northern Ireland, UK.
Gastroenterology. 2012 Feb;142(2):233-40. doi: 10.1053/j.gastro.2011.10.034. Epub 2011 Nov 4.
BACKGROUND & AIMS: Esophageal adenocarcinoma arises from Barrett's esophagus (BE); patients with this cancer have a poor prognosis. Identification of modifiable lifestyle factors that affect the risk of progression from BE to esophageal adenocarcinoma might prevent its development. We investigated associations among body size, smoking, and alcohol use with progression of BE to neoplasia.
We analyzed data from patients with BE identified from the population-based Northern Ireland BE register, diagnosed between 1993 and 2005 with specialized intestinal metaplasia (n = 3167). Data on clinical, demographic, and lifestyle factors related to diagnosis of BE were collected from hospital case notes. We used the Northern Ireland Cancer Registry to identify which of these patients later developed esophageal adenocarcinoma, adenocarcinomas of the gastric cardia, or esophageal high-grade dysplasia. Cox proportional hazards models were used to associate lifestyle factors with risk of progression.
By December 31, 2008, 117 of the patients with BE developed esophageal high-grade dysplasia or adenocarcinomas of the esophagus or gastric cardia. Current tobacco smoking was significantly associated with an increased risk of progression (hazard ratio = 2.03; 95% confidence interval, 1.29-3.17) compared with never smoking, and across all strata of smoking intensity. Alcohol consumption was not related to risk of progression. Measures of body size were infrequently reported in endoscopy reports, and body size was not associated with risk of progression.
Smoking tobacco increases the risk of progression to cancer or high-grade dysplasia 2-fold among patients with BE, compared with patients with BE that have never smoked. Smoking cessation strategies should be considered for patients with BE.
食管腺癌起源于 Barrett 食管(BE);患有这种癌症的患者预后较差。确定影响 BE 向食管腺癌进展的可改变生活方式因素可能有助于预防其发生。我们研究了体重、吸烟和饮酒与 BE 进展为肿瘤之间的关联。
我们分析了 1993 年至 2005 年间在基于人群的北爱尔兰 BE 登记处诊断出的具有特殊肠化生的 BE 患者(n=3167)的人群中发现的 BE 患者的数据。从医院病历中收集了与 BE 诊断相关的临床、人口统计学和生活方式因素的数据。我们使用北爱尔兰癌症登记处来确定这些患者中哪些人后来发展为食管腺癌、胃贲门腺癌或食管高级别异型增生。使用 Cox 比例风险模型将生活方式因素与进展风险相关联。
截至 2008 年 12 月 31 日,117 例 BE 患者发展为食管高级别异型增生或食管或胃贲门腺癌。与从不吸烟的患者相比,当前吸烟与进展风险增加显著相关(风险比=2.03;95%置信区间,1.29-3.17),并且在所有吸烟强度分层中均如此。饮酒与进展风险无关。体重指标在内镜报告中很少报告,并且体重与进展风险无关。
与从未吸烟的 BE 患者相比,吸烟会使 BE 患者发展为癌症或高级别异型增生的风险增加 2 倍。应考虑为 BE 患者实施戒烟策略。