Evidence map›Paper›PMID 42226290›Full record

ArticleWorld journal of surgical oncology2026

Development and validation of a machine learning model for predicting distant metastasis in patients with renal cell carcinoma: a population-based study.

Cheng Cheng, Xiongwu Peng, Rongli Qiu, Haidong Ma, Mengyu Gui, Runlin Shi

Abstract readValidation Study
In one paragraph

Article in World journal of surgical 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cheng Cheng *Department of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Xiongwu Peng *Department of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Rongli Qiu *Department of Urology, Zhangshu People's Hospital, Yichun, Jiangxi Province, China.
Haidong MaDepartment of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Mengyu GuiDepartment of Respiratory Medicine, De'an County People's Hospital, Jiujiang, Jiangxi Province, China.
Runlin ShiDepartment of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China. shanshupai@163.com.

Funding

The Natural Science Foundation of Jiangxi Province 20242BAB20420
6 · The paper itself

Abstract

backgroundDistant metastasis is the leading cause of death in renal cell carcinoma (RCC), yet accurate prediction tools remain lacking. We aimed to develop and validate a machine learning model to predict synchronous distant metastasis-defined as metastasis present at the time of initial diagnosis-in RCC.

methodsWe identified 106,448 RCC patients from the SEER database (2010-2020), divided into training (n = 52,368), internal validation (n = 22,444), and external validation (n = 31,636) cohorts. Nine machine learning algorithms were compared using area under the curve (AUC), calibration, and decision curve analysis. Model interpretability was assessed using SHAP analysis.

resultsDistant metastasis was present in 10.7% of patients. N1 stage (OR 8.28-9.46), tumor size > 7 cm (OR 6.30-7.72), T4 stage (OR 6.29-8.51), and sarcomatoid histology (OR 1.89-3.28) were independent risk factors, while chromophobe histology (OR 0.04-0.11) and multifocal tumors (OR 0.40-0.53) were protective. Gradient Boosting achieved AUCs of 0.906, 0.906, and 0.926 in training, internal, and external validation cohorts, respectively. The model demonstrated good calibration and clinical utility across threshold probabilities of 5%-80%. Performance remained stable across subgroups and sensitivity analyses. A web calculator was developed ( https://952307952pxw.shinyapps.io/RCC-Calculator/ ).

conclusionsWe developed a machine learning model that accurately predicts synchronous distant metastasis at the time of initial RCC diagnosis, with good generalizability. The online calculator may assist clinicians in risk stratification and individualized decision-making.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsMachine LearningAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingPrediction AlgorithmsPredictive Learning ModelsPrognosisRisk FactorsDistant metastasisMachine learningPrediction modelRenal cell carcinomaSEER

Identifiers

PMID42226290
PMCPMC13455490

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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.