Evidence map›Paper›PMID 42304264›Full record

ArticleBMC pediatrics2026

Machine learning model based on clinical and imaging features for predicting fungal infections in children with leukemia.

Peng Ge, Xu-Sheng Qian, Yu He, Ya-Kang Dai, Wan-Liang Guo

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Article in BMC pediatrics, 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

Authors and funding

5 authors.

Peng GeDepartment of Radiology, Children's Hospital of Soochow University, Suzhou, 215025, China.
Xu-Sheng QianSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China.
Yu HeDepartment of Radiology, Children's Hospital of Soochow University, Suzhou, 215025, China.
Ya-Kang DaiSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China. daiyk@sibet.ac.cn.
Wan-Liang GuoDepartment of Radiology, Children's Hospital of Soochow University, Suzhou, 215025, China. gwlsuzhou@163.com.

Funding

Suzhou Medical Key Discipline No. SZXK202510Suzhou Science & Technology Projects SZS2024007
6 · The paper itself

Abstract

backgroundDue to immunosuppression, mucosal barrier injury, and prolonged neutropenia resulting from both the disease and chemotherapy, along with the frequent use of broad-spectrum antibiotics and glucocorticoids, children with leukemia are at a high risk of invasive fungal disease (IFD). The present study aimed to develop an effective machine learning model to predict fungal infections in children with leukemia.

methodsA total of 247 pediatric patients diagnosed with leukemia and concurrent infections were evaluated. Five distinct ML classifiers-Random Forest, Logistic Regression, Support Vector Machine (SVM), Naïve Bayes, and K-Nearest Neighbors-were employed to construct predictive classification models. These models were trained using three distinct feature sets: (1) clinical features exclusively, (2) imaging features exclusively, and (3) an integrated feature set comprising both clinical and imaging data. The predictive model was validated prospectively in an independent cohort of 61 patients. Model performance was evaluated through cross-validation techniques to ensure robustness and generalizability. To validate the clinical applicability of the ML models, their diagnostic performance was systematically compared against that of three radiologists with varying experience levels: Reader A (3 years), Reader B (6 years), and Reader C (11 years).

resultsAmong the five classifiers evaluated, models using both clinical and imaging features consistently outperformed those relying solely on either clinical or imaging features. Notably, the SVM algorithm exhibited the highest overall predictive performance. Within the SVM algorithm, the validation set achieved the mean area under the curve (AUC) values of 0.825 with clinical features alone, 0.852 with imaging features alone, and 0.947 when both clinical and imaging features were combined. The corresponding mean AUC values for the test set were 0.777, 0.797, and 0.879. Furthermore, a comparative analysis between the classification results of the SVM model and the diagnostic assessments provided by three radiologists demonstrated that the SVM consistently outperformed the radiologists across key performance metrics.

conclusionsThe SVM algorithm demonstrates robust efficacy in predicting fungal infections among pediatric patients diagnosed with leukemia. Within the predictive model, the variables that exhibited the greatest influence included pleural thickening, neutropenia, hormone therapy, CRP level, mediastinal lymphadenopathy, and the presence of pleural effusion.

Indexed as

Invasive Fungal InfectionsLeukemiaMachine LearningMycosesAdolescentBayes TheoremChildChild, PreschoolClassification AlgorithmsFemaleHumansLogistic ModelsMalePrecursor Cell Lymphoblastic Leukemia-LymphomaPrediction AlgorithmsPredictive Learning ModelsFungal infectionsMachine learningPediatric leukemiaRisk factors

Identifiers

PMID42304264
PMCPMC13629111

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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.