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基线筛查时诊断为轻度非肿瘤性病变的患者能否安全地免于监测:来自多中心社区队列的证据。

Can patients with mild non-neoplastic lesions diagnosed at baseline screening be safely exempt from surveillance: evidence from multicenter community-based cohorts.

作者信息

He Siyi, Zhang Zhiyi, Song Guohui, Wang Zhenhai, Dai Chunyun, Yan Shipeng, Jiang Kun, Song Bingbing, Li He, Cao Maomao, Sun Dianqin, Yang Fan, Yan Xinxin, Zhang Shaoli, Teng Yi, Li Qianru, Xia Changfa, Chen Wanqing

机构信息

Office of Cancer Screening, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

Department of Gastroenterology, Gansu Wuwei Tumor Hospital, Wuwei, 730000, China.

出版信息

Sci China Life Sci. 2025 Jan;68(1):263-271. doi: 10.1007/s11427-023-2558-x. Epub 2024 Sep 6.

Abstract

Surveillance recommendations for gastric cancer (GC) in current guidelines focused on advanced precancerous lesions and were based on precise diagnosis of severity/extent of baseline lesions. We aimed to develop a less endoscopy-related equipment-dependent risk-stratification tool, and assessed whether mild-precursor-lesion patients can be safely exempt from surveillance. In the multicenter community-based cohort, 75,051 participants receiving baseline endoscopy were enrolled during 2015-2017 and followed-up until 2021. Cumulative incidence rates (CIRs) of GC for precancerous-conditions were calculated by Kaplan-Meier method and compared by Log-rank tests. Mixed-effects Cox regression models were used to detect potential factors for progression towards GC. A risk score was calculated as counts of selected factors. An independent cohort, including 26,586 participants was used for external validation. During a median follow-up of 6.25 years, CIRs of GC were 0.302%, 0.436%, and 4.756% for normal group, non-neoplastic (atrophic gastritis/intestinal metaplasia) and neoplastic lesions (low-grade/high-grade dysplasia), respectively (P<0.001). Four predictors, including male, ⩾60 years, smoking, and limited vegetable consumption, were selected for risk-stratification. High-risk patients (⩾3 risk factors) with non-neoplastic lesions showed higher GC risks (adjusted HR=7.73, 95%CI: 4.29-13.92), and their four-year CIR reached the one-year CIR of neoplastic lesions. Further categorizing non-neoplastic lesions by histological grade, both patients with moderate-to-severe lesions (aHR=3.07, 95%CI: 1.67-5.64) and high-risk patients with mild lesions (aHR=7.29, 95%CI: 3.58-14.86) showed higher risks. Consistent trends were observed in validation cohort. High-risk mild-precursor-lesion patients should receive surveillance within 3-5 years after baseline screening. Our study provides evidence on supplementing current guideline recommendations.

摘要

当前指南中针对胃癌(GC)的监测建议侧重于晚期癌前病变,且基于对基线病变严重程度/范围的精确诊断。我们旨在开发一种较少依赖内镜相关设备的风险分层工具,并评估轻度前驱病变患者是否可安全免除监测。在基于社区的多中心队列研究中,2015年至2017年期间纳入了75,051名接受基线内镜检查的参与者,并随访至2021年。采用Kaplan-Meier方法计算癌前病变的胃癌累积发病率(CIRs),并通过对数秩检验进行比较。使用混合效应Cox回归模型检测向胃癌进展的潜在因素。将选定因素的计数计算为风险评分。一个包括26,586名参与者的独立队列用于外部验证。在中位随访6.25年期间,正常组、非肿瘤性病变(萎缩性胃炎/肠化生)和肿瘤性病变(低级别/高级别异型增生)的胃癌CIRs分别为0.302%、0.436%和4.756%(P<0.001)。选择男性、≥60岁、吸烟和蔬菜摄入量有限这四个预测因素进行风险分层。具有非肿瘤性病变的高危患者(≥3个风险因素)显示出较高的胃癌风险(调整后HR=7.73,95%CI:4.29-13.92),其四年CIR达到肿瘤性病变的一年CIR。按组织学分级对非肿瘤性病变进一步分类,中度至重度病变患者(调整后HR=3.07,95%CI:1.67-5.64)和轻度病变高危患者(调整后HR=7.29,95%CI:3.58-14.86)均显示出较高风险。在验证队列中观察到一致趋势。高危轻度前驱病变患者应在基线筛查后3至5年内接受监测。我们的研究为补充当前指南建议提供了证据。

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