Xiao Shiyu, Lu Haoping, Xue Yan, Cui Rongli, Meng Lingmei, Jin Zhu, Yin Zhihao, Zhou Liya
Department of Gastroenterology, Peking University Third Hospital, Beijing, China; Beijing Key Laboratory of Helicobacter pylori Infection and Upper Gastrointestinal Diseases, Peking University Third Hospital, Beijing China.
Department of Gastroenterology, Peking University Third Hospital, Beijing, China; Beijing Key Laboratory of Helicobacter pylori Infection and Upper Gastrointestinal Diseases, Peking University Third Hospital, Beijing China.
Clin Gastroenterol Hepatol. 2022 Jun;20(6):1259-1268.e7. doi: 10.1016/j.cgh.2021.10.032. Epub 2021 Oct 28.
BACKGROUND & AIMS: The natural course of gastric mild-moderate dysplasia in a country with high incidence of gastric cancer (GC) is relatively unknown. We aimed to determine the long-term cumulative incidence of and risk factors for advanced neoplasia in patients with gastric dysplasia.
This was a single-center observational study including all consecutive patients diagnosed with gastric mild-moderate dysplasia between 2000 and 2017. Follow-up data were collected until December 2019. We determined the cumulative incidence of advanced neoplasia and identified risk factors with Cox regression.
A total of 3489 consecutive participants were followed for a median of 4.19 years from initial mild-moderate dysplasia diagnosis. The median surveillance interval between index endoscopy and next follow-up endoscopy was 1.08 years, and more than half of patients had at least 3 surveillance gastroscopies. During the study period, the majority of participants did not show disease progression, either with dysplasia not detected (51.4%) or with persistent dysplasia (46.1%). There were 88 (2.9%) patients (5.13 per 1000 patient-years) who progressed to advanced neoplasia within a median of 4.3 years. The annual incidence of advanced neoplasia and GC were 0.43% and 0.26%, respectively, within 5 years of mild-moderate dysplasia diagnosis. Increasing age, male sex, moderate dysplasia, dysplasia detected in fundus or cardia at index endoscopy, and persistent Helicobacter pylori infection during follow-up were independent risk factors for developing advanced neoplasia.
Even in a country with high incidence of GC, the majority of patients with gastric mild-moderate dysplasia did not experience disease progression in the long term. Intensified surveillance during the first 5 years after mild-moderate dysplasia detection is suggested.
在胃癌(GC)高发国家,胃轻-中度发育异常的自然病程相对尚不明确。我们旨在确定胃发育异常患者发生高级别肿瘤的长期累积发生率及危险因素。
这是一项单中心观察性研究,纳入了2000年至2017年间所有连续诊断为胃轻-中度发育异常的患者。随访数据收集至2019年12月。我们确定了高级别肿瘤的累积发生率,并通过Cox回归识别危险因素。
从最初诊断为胃轻-中度发育异常起,共对3489名连续参与者进行了中位时间为4.19年的随访。初次内镜检查与下一次随访内镜检查之间的中位监测间隔为1.08年,超过半数患者至少接受了3次监测胃镜检查。在研究期间,大多数参与者未出现疾病进展,要么未检测到发育异常(51.4%),要么发育异常持续存在(46.1%)。有88名(2.9%)患者(每1000患者年5.13例)在中位时间4.3年内进展为高级别肿瘤。在胃轻-中度发育异常诊断后的5年内,高级别肿瘤和胃癌的年发生率分别为0.43%和0.26%。年龄增加、男性、中度发育异常、初次内镜检查时在胃底或贲门发现发育异常以及随访期间幽门螺杆菌持续感染是发生高级别肿瘤的独立危险因素。
即使在胃癌高发国家,大多数胃轻-中度发育异常患者长期未出现疾病进展。建议在检测到胃轻-中度发育异常后的前5年加强监测。