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

Peng Ge1, Xu-Sheng Qian2, Yu He1

  • 1Department of Radiology, Children's Hospital of Soochow University, Suzhou, 215025, China.

BMC Pediatrics
|June 17, 2026
PubMed

Insights

A machine learning model effectively predicts invasive fungal disease (IFD) in children with leukemia. The Support Vector Machine (SVM) algorithm, using combined clinical and imaging data, outperformed radiologists in identifying infections.

Area of Science:

  • Oncology
  • Medical Imaging
  • Machine Learning

Background:

  • Children with leukemia face high risks of invasive fungal disease (IFD) due to immunosuppression and other factors.
  • Predicting IFD in this vulnerable population is crucial for timely intervention.

Purpose of the Study:

  • To develop and validate a machine learning (ML) model for predicting fungal infections in pediatric leukemia patients.
  • To compare the diagnostic performance of the ML model against experienced radiologists.

Main Methods:

  • Evaluated 247 pediatric leukemia patients with infections using five ML classifiers (Random Forest, Logistic Regression, SVM, Naïve Bayes, KNN).
  • Trained models using clinical features, imaging features, or a combination of both.
  • Prospectively validated the best model in an independent cohort of 61 patients and compared its performance against three radiologists.

Main Results:

  • Models integrating both clinical and imaging features showed superior performance compared to those using single data types.
  • The Support Vector Machine (SVM) algorithm achieved the highest predictive performance, with a combined AUC of 0.947 in the validation set.
  • The SVM model consistently outperformed radiologists in diagnostic accuracy for predicting fungal infections.

Conclusions:

  • The SVM algorithm is highly effective for predicting fungal infections in pediatric leukemia patients.
  • Key predictive variables include pleural thickening, neutropenia, hormone therapy, CRP level, mediastinal lymphadenopathy, and pleural effusion.
Abstract

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