Large-Scale Pre-training Enables Multimodal AI Differentiation of Radiation Necrosis from Brain Metastasis Progression on Routine MRI

TL;DR

This study demonstrates that large-scale self-supervised pre-training of Vision Transformers on unlabeled MRI data significantly enhances AI's ability to differentiate radiation necrosis from tumor progression in brain metastases, outperforming traditional methods.

Contribution

The paper introduces a two-phase deep learning approach using self-supervised pre-training on large unlabeled datasets, improving accuracy and interpretability in MRI-based differentiation tasks.

Findings

Self-supervised model achieved AUC 0.916 on internal test set.

Model outperformed fully supervised ViT and radiomics methods.

Multimodal integration further increased AUC to 0.947.

Abstract

Background: Differentiating radiation necrosis (RN) from tumor progression after stereotactic radiosurgery (SRS) remains a critical challenge in brain metastases. While histopathology represents the gold standard, its invasiveness limits feasibility. Conventional supervised deep learning approaches are constrained by scarce biopsy-confirmed training data. Self-supervised learning (SSL) overcomes this by leveraging the growing availability of large-scale unlabeled brain metastases imaging datasets. Methods: In a two-phase deep learning strategy inspired by the foundation model paradigm, a Vision Transformer (ViT) was pre-trained via SSL on 10,167 unlabeled multi-source T1CE MRI sub-volumes. The pre-trained ViT was then fine-tuned for RN classification using a two-channel input (T1CE MRI and segmentation masks) on the public MOLAB dataset (n=109) using 20% of datasets as same-center held-out test set. External validation was performed on a second-center test cohort (n=28). Results: The self-supervised model achieved an AUC of 0.916 on the same-center test set and 0.764 on the second center test set, surpassing the fully supervised ViT (AUC 0.624/0.496; p=0.001/0.008) and radiomics (AUC 0.807/0.691; p=0.005/0.014). Multimodal integration further improved performance (AUC 0.947/0.821; p=0.073/0.001). Attention map visualizations enabled interpretability showing the model focused on clinically relevant lesion subregions. Conclusion: Large-scale pre-training on increasingly available unlabeled brain metastases datasets substantially improves AI model performance. A two-phase multimodal deep learning strategy achieved high accuracy in differentiating radiation necrosis from tumor progression using only routine T1CE MRI and standard clinical data, providing an interpretable, clinically accessible solution that warrants further validation.