ArticleFrontiers in oncology2025
Personalized ICU mortality assessment by interpretable machine learning algorithms in patients with sepsis combined lung cancer: a population-based study and an external validation cohort.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Artificial intelligence for early sepsis detection and dynamic prognostication in onco-critical care.World journal of critical care medicine · 2026Review
- Construction and validation of a machine learning-based prediction model for in-hospital acute kidney injury in patients with lung cancer complicated with sepsis: clinical and nursing applications.Journal of thoracic disease · 2026Article
- Artificial Intelligence Models for Mortality and Outcome Prediction in Intensive Care Unit Sepsis: A Systematic Review.Journal of personalized medicine · 2026Review
- Development and validation of an explainable machine learning model for mortality prediction in ICU patients with lung cancer.Frontiers in cell and developmental biology · 2026Article
- Construction and validation of a prognostic prediction model for critically ill lung cancer patients based on respiratory functional reserve and systemic inflammatory characteristics.American journal of cancer research · 2026Article
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Authors and funding
3 authors.
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Abstract
Purpose: Sepsis is a leading cause of mortality, especially among immunocompromised patients with lung cancer. We aimed to establish machine learning (ML) based model to accurately forecast ICU mortality in patients with sepsis combined lung cancer. Methods: We incorporated patients with sepsis combined lung cancer from Medical Information Mart for Intensive Care IV (MIMIC IV) database. Univariate and multivariate logistic analysis were employed to select variables. Recursive Feature Elimination (RFE) method based on 6 ML algorithms was used for feature selection. We harnessed 13 ML algorithms to construct prediction model, which were assessed by area under the curve (AUC), accuracy, sensitivity, specificity, precision, cross-entropy and Brier scores. The best ML model was constructed to predict ICU mortality, and the predictive results were interpretated by SHapley Additive exPlanations (SHAP) framework. Results: A sum of 1096 lung cancer patients combined sepsis from MIMIC IV database and 251 patients from the external validation set were included. We utilized 13 clinical variables to establish prediction model for ICU mortality. CatBoost model was identified as the prime prediction model with the highest AUC in the training (0.931 [0.921, 0.945]), internal validation (0.698 [0.673, 0.724]) and external validation (0.794 [0.725, 0.879]) cohorts. Oxford Acute Severity of Illness Score (OASIS) had the greatest influence on ICU mortality according to SHAP interpretation. Conclusions: Our ML models demonstrate excellent accuracy and reliability, facilitating more rigorous personalized prognostic forecast to lung cancer patients combined sepsis.
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