Advanced imaging characterization of post-chemoradiation glioblastoma stratified by diffusion MRI phenotypes known to predict favorable anti-VEGF response
Year: 2025
Type: article
Study design: Observational Study
Abstract: Purpose Recurrent glioblastomas showing a survival benefit from anti-VEGF agents are known to exhibit a distinct diffusion MRI phenotype. We aim to characterize advanced imaging features of this glioblastoma subset. Methods MRI scans from 87 patients with IDH-wildtype glioblastoma were analyzed. All patients had completed standard chemoradiation and were anti-VEGF-naïve. Contrast-enhancing tumor segmentations were used to extract: the lowest peak of the double gaussian distribution of apparent diffusion coefficient values (ADC L ) calculated from diffusion MRI, relative cerebral blood flow (rCBV) values from perfusion MRI, MTR asym @ 3ppm from pH-weighted amine CEST MRI, quantitative T 2 and T 2 * relaxation times (qT 2 and qT 2 *), T 1 w subtraction map values, and contrast-enhancing tumor volume. Lesions were categorized as high- or low-ADC L using a cutoff of 1240 µm 2 /s, according to previous studies. Results High-ADC L lesions showed significantly lower rCBV (1.02 vs. 1.28, p = 0.0057), higher MTR asym @ 3ppm (2.36% vs. 2.10%, p = 0.0043), and higher qT 2 (114.8 ms vs. 100.9 ms, p = 0.0094), compared to low-ADC L lesions. No group differences were seen in contrast-enhancing tumor volume, T 1 w subtraction map values, and qT 2 *, nor in clinical variables such as sex category, MGMT status, and EGFR status. Finally, no clear group-specific preferential locations were seen. Conclusion Post-chemoradiation glioblastomas with a diffusion MRI phenotype that is known to predict a favorable response to anti-VEGF (ADC L ≥1240 µm 2 /s) have distinct biological features, with different perfusion and metabolic characteristics, and T 2 relaxation times.
Source: Journal of Neuro-Oncology
Authors: Francesco Sanvito, Irina Kryukov, Jingwen Yao, Ashley Teraishi, Catalina Raymond, John Gao, Cole Miller, Phioanh L. Nghiemphu, Albert Lai, Linda M. Liau, Kunal Patel, Richard G. Everson, Blaine S.C. Eldred, Robert M. Prins, David A. Nathanson, Noriko Salamon, Timothy F. Cloughesy, Benjamin M. Ellingson
Institution: University of California, Los Angeles
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,590
OpenAlex ID: W4409407957
