Evidence map›Paper›PMID 42908942›Full record

ArticleFrontiers in medicine2026

Development and internal validation of a predictive model for clinical deterioration in newly diagnosed lung cancer patients based on interpretable machine learning.

Huiling Li, Yin Li, Xiaomin Huang, Zelian Zhang, Qianfei Liu, Quanfang Chen

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Article in Frontiers in medicine, 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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6 authors.

Huiling Li *Department of Respiratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Yin Li *Department of Respiratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Xiaomin HuangDepartment of Pulmonary and Critical Care Medicine, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi City, Hu Bei, China.
Zelian ZhangDepartment of Pulmonary and Critical Care Medicine, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi City, Hu Bei, China.
Qianfei LiuDepartment of Respiratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Quanfang ChenDepartment of Respiratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To develop and validate an interpretable machine learning-based model for the early identification of the risk of clinical deterioration during hospitalization in newly diagnosed lung cancer patients. Methods: Clinical data of patients with newly diagnosed lung cancer admitted between July 2023 and December 2025 were retrospectively collected in this single-center study. A hybrid feature selection strategy integrating least absolute shrinkage and selection operator (LASSO) regression and the Boruta algorithm was employed to identify key predictors. Logistic regression (LR), random forest (RF), extreme gradient boosting (XGBoost), and support vector machine (SVM) models were constructed. Model performance was evaluated using the area under the receiver operating characteristic curve (AUC-ROC), calibration curves, and decision curve analysis (DCA). SHapley Additive exPlanations (SHAP) values were further applied to interpret the model's decision-making process. Results: A total of 1,001 newly diagnosed lung cancer patients were included, comprising 121 patients (12.1%) in the deterioration group and 880 patients (87.9%) in the non-deterioration group. Through the hybrid feature selection approach, five core predictive variables were identified, including Activities of Daily Living (ADL) score, lymphocyte count, C-reactive protein (CRP), respiratory rate, and neutrophil count. Among the models, the SVM model achieved the highest observed AUC of 0.822 (95% CI: 0.737-0.899) in the internal validation set, with a sensitivity of 0.750 (95% CI: 0.594-0.893) and a specificity of 0.792 (95% CI: 0.740-0.838). After Platt scaling calibration, the model achieved a Brier score of 0.083 (Hosmer-Lemeshow Conclusion: The SVM model developed in this study may help identify patients at risk of clinical deterioration among hospitalized lung cancer patients and may assist healthcare professionals in achieving early risk identification and potential clinical decision support.

Indexed as

ADL scoreclinical deteriorationlung cancermachine learningrisk predictionshap

Identifiers

PMID42908942
PMCPMC13683618

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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.