Evidence map›Paper›PMID 42661703›Full record

ArticleFrontiers in oncology2026

Interpretable machine learning prognostication of gastroenteropancreatic neuroendocrine tumors across Chinese and United States cohorts.

Yangwei Fan, Yuqian Yang, Ke Wang, Tian Zhang, Xuyuan Dong, Yu Shi, Meichen Wang, Enxiao Li, Yinying Wu

Abstract read
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Article in Frontiers in oncology, 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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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Yangwei FanDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Yuqian YangThe Affiliated Hospital of Northwest University, Xi'an No.3 Hospital, Xi'an, Shaanxi, China.
Ke WangDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Tian ZhangSchool of Physics, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Xuyuan DongDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Yu ShiDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Meichen WangDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Enxiao LiDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Yinying WuDepartment of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) display marked clinical heterogeneity, and conventional prognostic indicators such as TNM stage and Ki-67 index provide limited individualized risk discrimination. We aimed to develop and externally validate interpretable machine learning models for survival prediction. Methods: This retrospective study enrolled 337 patients with histologically confirmed GEP-NETs, randomly partitioned into a training set (n = 236) and an independent test set (n = 101) with stratification by mortality. Six survival models, including unpenalized Cox regression as a baseline, LASSO Cox, random survival forest (RSF), gradient-boosted survival analysis (GBSA), Extra Trees, and DeepSurv, were trained with 5×5 nested cross-validation. Discrimination, probabilistic accuracy, calibration, and clinical utility were comprehensively evaluated. SHAP analysis identified key predictors and informed nomogram construction. External validation was performed in 51,225 SEER patients. Results: On the test set, Extra Trees achieved the highest discrimination (C-index 0.843, 95% CI 0.762-0.914) and balanced calibration (1-year ICI 0.031). Time-dependent AUC values were 0.871, 0.847 and 0.935 at 1, 3 and 5 years. The Extra Trees-based stratification identified high-risk patients with substantially worse survival (HR 8.93, 95% CI 3.35-23.84, P<0.001). The model outperformed TNM stage (C-index 0.772), Ki-67 (0.705) and tumor grade (0.699). Decision curve analysis demonstrated greater net benefit across threshold probabilities of 5%-50%. SHAP analysis identified T stage, tumor grade, M1 status, TNM stage and Ki-67 as the top predictors. External validation in SEER preserved discriminative ability (C-index 0.719) and excellent calibration (slopes 0.901-1.058). Conclusion: Interpretable machine learning models outperform conventional approaches in predicting GEP-NET survival. Extra Trees showed the best internal discrimination and calibration, whereas DeepSurv achieved the highest external C-index. The simplified SHAP-derived nomogram provides a practical and well-calibrated but exploratory tool for individualized prognosis that requires prospective validation before clinical use.

Indexed as

external validationgastroenteropancreatic neuroendocrine tumorsmachine learningSHAPsurvival prediction

Identifiers

PMID42661703
PMCPMC13518172

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