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Development and Validation of the Early Gastric Carcinoma Prediction Model in Post-Eradication Patients with Intestinal Metaplasia

医学 内科学 队列 接收机工作特性 人口 癌症 肠化生 幽门螺杆菌 胃肠病学 肿瘤科 人工智能 计算机科学 环境卫生
作者
Wulian Lin,Guanpo Zhang,Hong Chen,Wen Huang,Guilin Xu,Yunmeng Zheng,Chao Gao,Jin Zheng,Dazhou Li,Wen Wang
出处
期刊:Cancers [Multidisciplinary Digital Publishing Institute]
卷期号:17 (13): 2158-2158
标识
DOI:10.3390/cancers17132158
摘要

Background: Gastric cancer (GC) remains a major global health challenge, with rising incidence among patients post-Helicobacter pylori (H. pylori) eradication, particularly those with persistent intestinal metaplasia (IM). Current risk stratification tools are limited in this high-risk population. Aim: To develop, validate, and externally test a machine learning-based prediction model—termed the Early Gastric Cancer Model (EGCM)—for identifying early gastric cancer (EGC) risk in H. pylori-eradicated patients with IM, and to implement it as a web-based clinical tool. Methods: This retrospective, dual-center study enrolled 214 H. pylori-eradicated patients with histologically confirmed IM from 900 Hospital and Fujian Provincial People’s Hospital. The dataset was split into a training cohort (70%) and an internal validation cohort (30%), with an external test cohort from the second center. A total of 21 machine learning algorithms were screened using cross-validation and hyperparameter optimization. Boruta and SHAP analyses were employed for feature selection, and the final EGCM was constructed using the top five predictors: atrophy range, xanthoma, map-like redness (MLR), MLR range, and age. Model performance was evaluated via ROC curves, precision–recall curves, calibration plots, and decision curve analysis (DCA), and compared against conventional inflammatory biomarkers such as NLR and PLR. Results: The CatBoost algorithm demonstrated the best overall performance, achieving an AUC of 0.743 (95% CI: 0.70–0.80) in internal validation and 0.905 in the external test set. The EGCM exhibited superior discrimination compared to individual inflammatory markers (p < 0.01). Calibration analysis confirmed strong agreement between predicted and observed outcomes. DCA showed the EGCM yielded greater net clinical benefit. A web calculator was developed to facilitate clinical application. Conclusions: The EGCM is a validated, interpretable, and practical tool for stratifying EGC risk in H. pylori-eradicated IM patients across multiple centers. Its integration into clinical practice could improve surveillance precision and early cancer detection.
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