Evidence map›Paper›PMID 42814197›Full record

ArticleCancer causes & control : CCC2026

A machine learning model for distinguishing gastric cancer from intestinal metaplasia in patients with psychological symptoms.

Shi-Ran Wang, Yu-Quan Mao, Guo-Jie Hu

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Article in Cancer causes & control : CCC, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Shi-Ran WangDepartment of Traditional Chinese Medicine, The Affiliated Hospital of Qingdao University, No.16 Jiangsu Road, Shinan District, Qingdao, Shandong, China.ORCID http://orcid.org/0009-0009-6470-1555
Yu-Quan MaoDepartment of Traditional Chinese Medicine, The Affiliated Hospital of Qingdao University, No.16 Jiangsu Road, Shinan District, Qingdao, Shandong, China.ORCID http://orcid.org/0000-0003-4525-6811
Guo-Jie HuDepartment of Traditional Chinese Medicine, The Affiliated Hospital of Qingdao University, No.16 Jiangsu Road, Shinan District, Qingdao, Shandong, China. huguojie2003@163.com.ORCID http://orcid.org/0000-0001-9844-8548

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo develop and internally evaluate an interpretable machine learning model for distinguishing current gastric cancer (GC) from intestinal metaplasia (IM) among patients with psychological symptoms.

methodsThis retrospective, single-center, cross-sectional study included 302 patients with psychological symptoms, comprising 185 with IM and 117 with GC. Patients were randomly divided into a training cohort (n = 212) and an independently retained validation cohort (n = 90). Candidate features were evaluated using LASSO, Boruta, and recursive feature elimination. Seven machine learning algorithms were compared using nested cross-validation in the training cohort. The final model was assessed in the validation cohort using discrimination, calibration, decision curve analysis, and Shapley Additive Explanations (SHAP).

resultsSeven features were retained: age, albumin, sex, psychological symptom type, total bilirubin, smoking status, and monocyte count. XGBoost achieved the highest mean outer-fold AUC (0.839 ± 0.029) and was selected as the final model. In the validation cohort, XGBoost achieved an AUC of 0.793 (95% CI 0.670-0.895), accuracy of 0.800, sensitivity of 0.657, specificity of 0.891, and F1 score of 0.719. The Brier score was 0.167. Decision curve analysis suggested potential clinical net benefit. SHAP analysis identified age and psychological symptom type as the leading contributors to classification.

conclusionsThe interpretable XGBoost model showed moderate discrimination for distinguishing current GC from IM and may provide supplementary information for clinical assessment. It should not replace endoscopic or histopathological diagnosis, and external multicenter validation is required before broader clinical implementation.

Indexed as

Machine LearningMetaplasiaStomach NeoplasmsAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsCross-Sectional StudiesDiagnosis, DifferentialFemaleHumansMaleMiddle AgedPredictive Learning ModelsRetrospective StudiesGastric cancerIntestinal metaplasiaMachine learningPsychological symptomsSHAP

Identifiers

PMID42814197

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.