ASL-based Exchange Time Mapping for Differentiation of High-Grade Glioma and Brain Metastases

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ID: 322371
2026
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Abstract
Abstract Background To evaluate whether blood-brain barrier (BBB) mapping via arterial spin-labeling (ASL)-derived exchange time (Tex) can differentiate high-grade gliomas from brain metastases and to compare regional BBB alterations with dynamic susceptibility contrast (DSC)-derived leakage parameters (K2). Methods 18 patients with therapy-naive cerebral masses (11 gliomas, 7 metastases) underwent multi-echo-ASL and DSC perfusion MRI. Tex maps were obtained using a validated extended two-compartment model. K2 maps were derived from single-echo DSC. Tex and absolute K2 (|K2|) were quantified in contrast-enhancing tumor (CET), peritumoral T2/FLAIR hyperintense region (PTR), gray matter (GM), and white matter (WM). Regional differences were assessed using Wilcoxon signed-rank and Mann–Whitney U tests. Receiver operating characteristic (ROC) analyses evaluated discrimination between gliomas and metastases. Results Tex was significantly lower in PTR of gliomas versus metastases (p = 0.046). In ROC analysis, Tex slightly outperformed |K2| alone (AUC=0.792, 95% CI [0.535, 0.986] vs. AUC=0.760, 95% CI [0.508, 0.959]), with further improvement upon combination (AUC=0.833, 95% CI [0.577, 1.000]). In gliomas, Tex was significantly lower in CET than in GM and WM (both p < 0.01) and PTR showed significantly lower Tex than WM (p < 0.01). |K2| was significantly higher in CET than all other regions (all p < 0.01) but did not differ between PTR and GM/WM. Conclusion In this exploratory study, ASL-derived Tex suggests stronger BBB alterations in peritumoral tissue of high-grade gliomas compared with brain metastases. Adding |K2| further improved discrimination. This supports ASL-based BBB mapping as a complement to DSC leakage imaging. Validation in larger multicenter cohorts is warranted.
Reference Key
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Authors Philipp Raffler, Gabriel Hoffmann, Matthias Günther, Matthias J P van Osch, Lena Václavů, Amnah Mahroo, Stephan Kaczmarz, Benedikt Wiestler
Journal Neuro-Oncology Advances
Year 2026
DOI
10.1093/noajnl/vdag195
URL
https://doi.org/10.1093/noajnl/vdag195
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