Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Endoscopy. 2013;45(4):249-56. doi: 10.1055/s-0032-1326379. Epub 2013 Mar 26.
A recent international guideline recommends surveillance of premalignant gastric lesions for patients at risk of progression to gastric cancer. The aim of this study was to identify the role of the distribution and severity of premalignant lesions in risk categorization.
Patients with a previous diagnosis of atrophic gastritis, intestinal metaplasia, or low grade dysplasia were invited for surveillance endoscopy with non-targeted biopsy sampling. Biopsy specimens were evaluated by pathologists (four general and one expert) using the Sydney and the operative link for gastric intestinal metaplasia (OLGIM) systems, and scores were compared using kappa statistics.
140 patients were included. In 37 % (95 % confidence interval [CI] 29 % - 45 %) the severity of premalignant lesions was less than at baseline, while 6 % (95 %CI 2 % - 10 %) showed progression to more severe lesions. Intestinal metaplasia in the corpus was most likely to progress to more than one location (57 %; 95 %CI 36 % - 76 %). The proportion of patients with multilocated premalignant lesions increased from 24 % at baseline to 31 % at surveillance (P = 0.014). Intestinal metaplasia was the premalignant lesion most frequently identified in subsequent endoscopies. Intestinal metaplasia regressed in 27 % compared with 44 % for atrophic gastritis and 100 % for low grade dysplasia. Interobserver agreement was excellent for intestinal metaplasia (k = 0.81), moderate for dysplasia (k = 0.42), and poor for atrophic gastritis (k < 0).
Premalignant gastric lesions found in the corpus have the highest risk of progression, especially intestinal metaplasia, which has excellent interobserver agreement. This supports the importance of intestinal metaplasia as marker for follow-up in patients with premalignant gastric lesions.
最近的国际指南建议对有进展为胃癌风险的患者进行癌前胃病变的监测。本研究的目的是确定癌前病变的分布和严重程度在风险分类中的作用。
邀请以前诊断为萎缩性胃炎、肠上皮化生或低级别上皮内瘤变的患者进行非靶向活检采样的监测内窥镜检查。病理学家(四位普通病理学家和一位专家病理学家)使用悉尼和胃肠上皮化生操作链接(OLGIM)系统评估活检标本,并使用 Kappa 统计比较评分。
共纳入 140 例患者。在 37%(95%置信区间 [CI] 29%-45%)的患者中,癌前病变的严重程度低于基线,而 6%(95%CI 2%-10%)的患者进展为更严重的病变。胃体的肠上皮化生最有可能进展到多个部位(57%;95%CI 36%-76%)。癌前多部位病变患者的比例从基线时的 24%增加到监测时的 31%(P=0.014)。肠上皮化生是随后内窥镜检查中最常发现的癌前病变。与萎缩性胃炎的 44%相比,肠上皮化生的消退率为 27%,而低级别上皮内瘤变的消退率为 100%。肠上皮化生的观察者间一致性极好(K=0.81),低级别上皮内瘤变的一致性为中度(K=0.42),萎缩性胃炎的一致性较差(K<0)。
胃体中发现的癌前胃病变进展风险最高,尤其是肠上皮化生,其观察者间一致性极好。这支持肠上皮化生作为癌前胃病变患者随访标志物的重要性。