Clinically meaningful risk factors for recurrence in T1 colorectal cancer treated with endoscopic resection alone identified by unsupervised machine learning: a multicenter study

医学 危险分层 结直肠癌 内科学 回顾性队列研究 结肠镜检查 多中心研究 决策树 肿瘤科 风险评估 分类器(UML) 切除术 放射科 队列研究 粘膜切除术 决策树学习 胃肠病学 外科 癌症 外科切除术 递归分区 结直肠外科 内窥镜检查 直肠 试验预测值 临床决策 病理 内镜黏膜下剥离术
作者
Xue Zhou,Kazutomo Togashi,Xin Zhu,Yoshiki Kajiwara,Shiro Oka,Shinji Tanaka,Manabu Takamatsu,Kinichi Hotta,Masayoshi Yamada,H Ikematsu,S Nagata,Kazutaka Yamada,K Hashimoto,Soichiro Ishihara,Yusuke Saitoh,Kenji Matsuda,Koji Komori,Megumi Ishiguro,Y Tamaru,Takashi Okuyama
出处
期刊:Endoscopy [Thieme Medical Publishers (Germany)]
标识
DOI:10.1055/a-2917-8805
摘要

Background: Identifying patients at high risk for recurrence after endoscopic resection of T1 colorectal cancer (CRC) remains challenging. This study aimed to identify recurrence risk subtypes and develop an interpretable risk stratification framework. Methods: This retrospective study analyzed 1123 patients with T1 CRC treated with endoscopic resection alone across 26 Japanese institutions (July 2009-December 2016). Patients were divided into development (68%) and evaluation (32%) cohorts based on institutional stratification. K-means clustering was applied to clinicopathologic variables to identify recurrence risk subtypes. A decision tree classifier was subsequently developed to generate transparent risk stratification rules. Results: Three distinct subtypes were identified in the development cohort. Subtype 1 exhibited a numerically higher recurrence rate (5.4%) than Subtype 2 (0.9%) and Subtype 3 (1.4%). Although subtypes 2 and 3 showed comparable recurrence rates, they were clearly differentiated by morphology (flat vs. polypoid). In the evaluation cohort, Subtype 1 continued to show a numerically higher recurrence (4.8%) compared with subtypes 2 (1.6%) and 3 (1.1%). The decision tree model stratified recurrence risk hierarchically: submucosal invasion <1000 μm indicated low risk, whereas invasion ≥1000 μm required morphologic assessment, with polypoid lesions classified as high risk and flat lesions further stratified using a 2000-μm threshold. Conclusions: Three clinically distinct recurrence risk subtypes were identified in T1 CRC following endoscopic resection, suggesting that morphologic subclassification of T1b lesions may refine stratification beyond conventional depth-based criteria. The decision framework offers a preliminary exploratory basis for recurrence risk assessment in this population.
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