Evidence map›Paper›PMID 41411039›Full record

ArticleJMIR medical informatics2025

A Machine Learning Approach to Predicting Mortality Risk in Chemotherapy-Treated Lung Cancer: Machine Learning Model Development and Validation.

Jianjun Zou, Jinyi Huang, Katie Lu, Ao Lin, Chen Xie, Jinrong Zhang, Boqi Rao, Zhi Li, Dongming Xie, Ling Lu and 7 more

Abstract read
In one paragraph

Article in JMIR medical informatics, 2025. 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

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Jianjun Zou *Institute of Tuberculosis, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0001-6274-5778
Jinyi Huang *School of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0007-5886-920X
Katie Lu *School of Medicine, University of Arizona, Tucson, AZ, United States.ORCID 0009-0000-8588-2505
Ao LinSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0001-7817-1617
Chen XieSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0000-1693-9993
Jinrong ZhangSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0004-4956-1404
Boqi RaoSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0002-9093-8064
Zhi LiSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0008-1277-7796
Dongming XieSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0007-6935-6709
Ling LuSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0003-9244-015X
Feng LuoSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0006-9343-0721
Jinbin ChenKingMed School of Laboratory Medicine, Guangzhou Medical University, Guangzhou, China.ORCID 0009-0001-6617-4471
Lei YangSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0002-1315-7651
Fuman QiuSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0003-2882-6413
Xin ZhangState Key Laboratory of Respiratory Disease, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0009-0007-7255-5557
Yibin DengCentre for Medical Laboratory Science, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.ORCID 0000-0002-0869-0400
Jiachun LuSchool of Public Health, Guangzhou Medical University, Guangzhou, Guangdong, China.ORCID 0000-0002-6189-826X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurately predicting the survival outcomes of patients with lung cancer receiving chemotherapy remains challenging.

objectiveTo improve clinical management of this population, this study developed a multivariate machine learning (ML) model to assess all-cause mortality risk in chemotherapy-treated patients with lung cancer.

methodsThis study retrospectively recruited 1278 postchemotherapy patients with lung cancer from Guangzhou Chest Hospital between 2017 and 2019. Candidate features such as demographic characteristics, environmental exposures, clinical information, and patient-reported symptoms were collected via questionnaires and the electronic medical record system. The survival status and the deceased date were investigated twice a year. A total of 84 predictive models were constructed on the training set using 5 ML algorithms either individually or in pairwise combinations. The concordance index was used to identify the optimal model on the testing set, with performance validated via receiver operating characteristic curves, calibration curves, and decision curve analysis. Additionally, Shapley Additive Explanations and restricted cubic splines were applied for feature attribution analysis.

resultsThe optimal model ultimately retained 21 prognosis-association features, including age, sex, BMI, smoking status, environmental smoke, the MD Anderson Symptom Inventory for Lung Cancer total score trajectories, cluster of differentiation 56, TNM stage, histology, and prechemotherapy blood biomarkers. On the testing set, the model acquired a concordance index of 0.702 (95% CI 0.652-0.753). The decision curves demonstrated positive clinical benefit when the risk thresholds were 0.40-0.69, 0.62-0.99, and 0.72-0.99 for 1-, 3-, and 5-year mortality predictions, respectively. The calibration curves showed that the predicted mortality probabilities fluctuated around the observed probabilities, and the Brier scores for 1-, 3-, and 5-year predictions were 0.20, 0.18, and 0.11, respectively. The area under the curve of the model was 0.740, 0.777, and 0.915 for 1-, 3-, and 5-year mortality predictions, respectively. Interpretability feature attribution analysis revealed that the significant features could predict all-cause mortality risk in chemotherapy-treated patients with lung cancer.

conclusionsOur ML models exhibited acceptable discrimination, calibration, and clinical benefit in predicting the mortality risk of chemotherapy-treated patients with lung cancer, which could help clinicians in personalized prognostic management.

Indexed as

Antineoplastic AgentsLung NeoplasmsMachine LearningAgedChinaFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesRisk AssessmentAntineoplastic Agentschemotherapylung cancermachine learningmortalityprediction model

Identifiers

PMID41411039
PMCPMC12757710

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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.