Treatment Effects of Different Therapeutic Strategies and Development of a Prognostic Prediction Model for Early Gastric Cancer: A Population-Based and Multicenter Study
5 affiliations
- 1Department of Gastroenterology, Jiangsu Province Hospital (the First Affiliated Hospital of Nanjing Medical University), Nanjing 210029, China
- 2Department of Gastroenterology, Hospital of Sihong, No. 31, Jiankang Road, Sihong 223900, China
- 3Endoscopy Center and Endoscopy Research Institute, Zhongshan Hospital, Fudan University & Shanghai Collaborative Innovation Center of Endoscopy, Shanghai 200032, China
- 4Department of Gastroenterology and Hepatology, Westmead Hospital, Sydney 2145, Australia
- 5Department of Gastroenterology, Chongqing Hospital of Jiangsu Province Hospital, Chongqing 401420, China
Abstract
Background: Early gastric cancer (EGC) lacks a predictive tool integrating endoscopic therapy (ET), gastrectomy (G), and chemoradiotherapy (CRT) to support individualized risk stratification. This study compared cancer-specific survival (CSS) and overall survival (OS) across the four treatment strategies and developed and externally validated a CSS prediction model incorporating oncologic characteristics and treatment strategy (presented as a nomogram and online tool). Methods: In a U.S. cohort (2017–2021), 1766 patients with EGC were classified into four treatments groups (ET, ET + CRT, G, G + CRT); an independent multicenter cohort (n = 1333) provided external validation. Kaplan–Meier curves, log-rank tests, and Cox regression assessed unadjusted differences, with confounding balanced by stabilized inverse probability of treatment weighting (sIPTW). Predictors were selected by univariable Cox, LASSO, Boruta, and best-subset regression; performance was evaluated by C-index, calibration curves, and decision curve analysis. Results: After sIPTW adjustment, CSS did not differ significantly between ET and G (p = 0.856), whereas G was associated with better CSS than G + CRT (p < 0.05). In exploratory analyses of node-positive patients, G + CRT was associated with lower cancer-specific mortality than G alone (p < 0.05). The CSS prediction model was validated internally and externally (AUCs for 1-, 3-, and 5-year CSS: 0.769, 0.737, 0.717 internally; 0.943, 0.890, 0.872 externally). Conclusions: This is the first externally validated EGC CSS model integrating all four treatments. For eligible patients, ET was associated with survival comparable to G and superior to G + CRT; among node-positive patients, G + CRT was associated with lower mortality than G alone. The model supports individualized prediction and treatment decisions.
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BibTeX
@article{jing2026treatment,
title = {{Treatment Effects of Different Therapeutic Strategies and Development of a Prognostic Prediction Model for Early Gastric Cancer: A Population-Based and Multicenter Study}},
author = {Ruiying Jing and Shimei Sun and Tian Tian and Zhiyu Xiang and Wei Su and Hunter Wang and Michael J. Bourke and Shengli Lin and Yaoyao Gong},
journal = {Cancers},
year = {2026},
month = oct,
doi = {10.3390/cancers18213488},
url = {https://www.mdpi.com/2072-6694/18/21/3488},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Treatment Effects of Different Therapeutic Strategies and Development of a Prognostic Prediction Model for Early Gastric Cancer: A Population-Based and Multicenter Study
AU - Ruiying Jing
AU - Shimei Sun
AU - Tian Tian
AU - Zhiyu Xiang
AU - Wei Su
AU - Hunter Wang
AU - Michael J. Bourke
AU - Shengli Lin
AU - Yaoyao Gong
PY - 2026
DA - 2026/10/29
JO - Cancers
DO - 10.3390/cancers18213488
UR - https://www.mdpi.com/2072-6694/18/21/3488
AB - Background: Early gastric cancer (EGC) lacks a predictive tool integrating endoscopic therapy (ET), gastrectomy (G), and chemoradiotherapy (CRT) to support individualized risk stratification. This study compared cancer-specific survival (CSS) and overall survival (OS) across the four treatment strategies and developed and externally validated a CSS prediction model incorporating oncologic characteristics and treatment strategy (presented as a nomogram and online tool). Methods: In a U.S. cohort (2017–2021), 1766 patients with EGC were classified into four treatments groups (ET, ET + CRT, G, G + CRT); an independent multicenter cohort (n = 1333) provided external validation. Kaplan–Meier curves, log-rank tests, and Cox regression assessed unadjusted differences, with confounding balanced by stabilized inverse probability of treatment weighting (sIPTW). Predictors were selected by univariable Cox, LASSO, Boruta, and best-subset regression; performance was evaluated by C-index, calibration curves, and decision curve analysis. Results: After sIPTW adjustment, CSS did not differ significantly between ET and G (p = 0.856), whereas G was associated with better CSS than G + CRT (p < 0.05). In exploratory analyses of node-positive patients, G + CRT was associated with lower cancer-specific mortality than G alone (p < 0.05). The CSS prediction model was validated internally and externally (AUCs for 1-, 3-, and 5-year CSS: 0.769, 0.737, 0.717 internally; 0.943, 0.890, 0.872 externally). Conclusions: This is the first externally validated EGC CSS model integrating all four treatments. For eligible patients, ET was associated with survival comparable to G and superior to G + CRT; among node-positive patients, G + CRT was associated with lower mortality than G alone. The model supports individualized prediction and treatment decisions.
SN - 2072-6694
ER -