GAN-Augmented Radiomics and Machine Learning for Post-Therapy GBM Progression Assessment.
Authors
Affiliations (14)
Affiliations (14)
- Department of Computer Science & Engineering, International Institute of Information Technology, Bhubaneswar, India.
- Department of Computer Science and Engineering, Indian Institute of Information Technology Vadodara, Vadodara, India.
- Department of Biotechnology and Chemical Engineering, School of Engineering, Faculty of Science, Technology and Architecture, Manipal University Jaipur, Dehmi Kalan, India.
- Infinity Insights Biotechnology Co., Ltd., Taipei, Taiwan.
- Faculty of Health Sciences, Shinawatra University, Pathum Thani, Thailand.
- University of Jember, Jember, Indonesia.
- Department of General Medicine, Subharti Medical College, Swami Vivekanand Subharti University, Meerut, India.
- Division of Neurosurgery, Department of Surgery, College of Medicine, Taipei Medical University, Taipei, Taiwan.
- TMU Neuroscience Research Center, Taipei Medical University, Taipei, Taiwan.
- Department of Neurosurgery, Taipei Medical University Hospital, Taipei, Taiwan.
- Taipei Neuroscience Institute, Taipei Medical University, Taipei, Taiwan.
- Division of Neurosurgery, Department of Surgery, College of Medicine, Taipei Medical University, Taipei, Taiwan. [email protected].
- TMU Neuroscience Research Center, Taipei Medical University, Taipei, Taiwan. [email protected].
- Department of Neurosurgery, Taipei Medical University Hospital, Taipei, Taiwan. [email protected].
Abstract
Differentiating true progression (TP) from pseudoprogression (PsP) in post-therapy of glioblastoma multiforme (GBM) remains a critical challenge in neuro-oncology, due to their overlapping radiological characteristics. Consequently, an accurate, non-invasive differentiation between PsP and TP is vital for informing treatment decisions and improving patient outcomes. Therefore, we aimed to present a comprehensive AI-driven framework integrating handcrafted radiomics, deep learning features, and generative modelling to enhance diagnostic precision. Multiparametric MRI data (T1, T2, FLAIR, T1GD) from 58 GBM patients (41 TP, 17 PsP) were analysed using three feature extraction strategies: handcrafted radiomics, Vision Transformer (ViT)-based deep features, and a hybrid combination of both. To address class imbalance, synthetic samples were generated using a Conditional Tabular Generative Adversarial Network (CT-GAN). Feature dimensionality was reduced through a two-stage pipeline comprising a Variational Autoencoder (VAE) followed by Principal Component Analysis (PCA), preserving 95% variance. Classifiers, including Support Vector Machine (SVM), Random Forest, XGBoost, and Multi-Layer Perceptron (MLP), were trained and validated via stratified 5-fold cross-validation. The radiomics-based SVM model yielded the best performance with an accuracy of 91.84% ± 3.59 (95% CI - 0.841 to 0.989) and an AUC of 0.9667 ± 0.0378 (95% CI - 0.920 to 0.998), demonstrating promising performance within the studied dataset and highlighting potential for clinical application, subject to further external validation. Our demonstrated CT-GAN-augmented hybrid radiomics framework offers a robust, non-invasive, and promising solution for reliably distinguishing PsP from TP. It shows promising performance within the studied dataset, with potential for future clinical translation subject to external validation.