This analysis identifies optimal pharmacokinetic models for glioblastoma regions, highlighting DCE-MRI's role in tumor assessment.
Motivation: Glioblastoma (GBM) has poor survival rates, and DCE-MRI aids in understanding tumor vascularity. However, selecting an optimal pharmacokinetic (PK) model remains challenging. Goal(s): To identify the best-fitting PK model for GBM regions using an Akaike Information Criterion (AIC)-based parsimonious model selection. Approach: DCE-MRI data from 46 GBM patients were segmented into enhancing, non-enhancing, and edema regions. Five PK models were fitted per region, with AIC used to select the best model per voxel. A parsimonious model was created from these best-fits. Results: The parsimonious model outperformed individual models across regions, with Extended Tofts, 2CXM and Shutter-Speed models excelling in enhancing/non-enhancing regions and edema. Impact: This study improves GBM assessment by optimizing DCE-MRI PK model selection. It tailors models to specific tumor regions, enabling more accurate quantification of tumor characteristics, aiding diagnosis & treatment planning. This approach can be applied to other tumors and imaging protocols.
No takes yet. Share an insight, caveat, or question.
Bera et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: