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PET and MRI Guided Irradiation of a Glioblastoma Rat Model Using a Micro-irradiator
Published on: December 28, 2017
Machine Learning-Driven radiomics on 18 F-FDG PET for glioma diagnosis: a systematic review and meta-analysis
Ali Shahriari1, Sasan Ghazanafar Ahari2, Ali Mousavi2
1Department of Radiation Oncology, Dana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, USA.
Background:
Machine learning (ML) applied to radiomics has revolutionized neuro-oncological imaging, yet the diagnostic performance of ML models based specifically on ^18F-FDG PET features in glioma remains poorly characterized.
Objective:
To systematically evaluate and quantitatively synthesize the diagnostic accuracy of ML models trained on ^18F-FDG PET radiomics for glioma classification.
Methods:
We conducted a PRISMA-compliant systematic review and meta-analysis registered on OSF ( https://doi.org/10.17605/OSF.IO/XJG6P ). PubMed, Scopus, and Web of Science were searched up to January 2025. Studies were included if they applied ML algorithms to ^18F-FDG PET radiomic features for glioma classification and reported at least one performance metric. Data extraction included demographics, imaging protocols, feature types, ML models, and validation design. Meta-analysis was performed using random-effects models with pooled estimates of accuracy, sensitivity, specificity, AUC, F1 score, and precision. Heterogeneity was explored via meta-regression and Galbraith plots.
Results:
Twelve studies comprising 2,321 patients were included. Pooled diagnostic metrics were: accuracy 92.6% (95% CI: 91.3-93.9%), AUC 0.95 (95% CI: 0.94-0.95), sensitivity 85.4%, specificity 89.7%, F1 score 0.78, and precision 0.90. Heterogeneity was high across all domains (I² >75%). Meta-regression identified ML model type and validation strategy as partial moderators. Models using CNNs or PET/MRI integration achieved superior performance.
Conclusion:
ML models based on ^18F-FDG PET radiomics demonstrate strong and balanced diagnostic performance for glioma classification. However, methodological heterogeneity underscores the need for standardized pipelines, external validation, and transparent reporting before clinical integration.
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