Development of a prognostic nomogram and risk factor analysis for survival in H. pylori-positive non-cardia gastric adenocarcinoma patients

构建幽门螺杆菌阳性非贲门胃腺癌患者生存预后列线图及风险因素分析

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Abstract

BACKGROUND: Currently, there is limited research on the prognosis and influencing factors of non-cardia gastric adenocarcinoma (NCGAC) patients. This study aims to explore the factors influencing overall survival (OS) in Helicobacter pylori (H. pylori)-positive NCGAC patients and to develop a nomogram model to provide guidance for clinicians. METHODS: We retrospectively analyzed clinicopathological data from 413 H. pylori-positive NCGAC patients who underwent radical gastrectomy at the General Hospital of Ningxia Medical University. The dataset was randomly split into a training cohort (70%) and a validation cohort (30%). Univariate Cox proportional hazards regression analysis was used to identify prognostic factors, and factors with multicollinearity [variance inflation factor (VIF) >4] were excluded using the VIF. Factors of interest and those with P<0.05 were included in the multivariate Cox proportional hazards regression model. A nomogram prediction model was constructed based on factors with P<0.05. The model's performance was finally assessed using the area under the receiver operating characteristic curve (AUC) and calibration curves. The Kaplan-Meier survival curves visualize the impact of independent prognostic factors. RESULTS: Univariate Cox regression analysis was performed on the training cohort to select variables with P<0.5, including alcohol consumption, tumor size, differentiation grade, lymph node metastasis, tumor (T) stage, node (N) stage, and tumor node metastasis (TNM) stage. Multicollinearity was assessed, and covariates with VIF >4, such as lymph node metastasis, were excluded. The remaining factors were included in the multivariate Cox regression model. Significant variables (P<0.05), including alcohol consumption, differentiation grade, and T stage, were used to construct a nomogram, which showed a concordance index (C-index) of 0.727 in the training cohort and 0.728 in the validation cohort. The model's performance was validated with AUC and calibration curves (training cohort: 1-year AUC: 0.74, 3-year AUC: 0.78, 4-year AUC: 0.80; validation cohort: 1-year AUC: 0.67, 3-year AUC: 0.71, 4-year AUC: 0.72). Kaplan-Meier survival curves illustrated the impact of independent prognostic factors. CONCLUSIONS: We developed a nomogram to predict survival in H. pylori-positive NCGAC patients, based on alcohol consumption, tumor differentiation, and T stage. The model showed strong predictive performance, with C-index values of 0.727 in the training cohort and 0.728 in the validation cohort. AUC values and calibration curves further confirmed its accuracy, suggesting the nomogram is a reliable tool for predicting prognosis and guiding treatment decisions.

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