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Updated: Mar 22, 2026

Tumor Treating Field Therapy in Combination with Bevacizumab for the Treatment of Recurrent Glioblastoma
Published on: October 27, 2014
Restriction spectrum imaging predicts response to bevacizumab in patients with high-grade glioma
Carrie R McDonald1, Rachel L Delfanti1, Anitha P Krishnan1
1Department of Psychiatry, University of California, San Diego, La Jolla, California (C.R.M., A.M.D.), Department of Radiology, University of California, San Diego, La Jolla, California (R.L.D., J.M.K., H.B., N.S.W., A.M.D., N.F.), Department of Radiation Medicine, University of California, San Diego, La Jolla, California (C.R.M., J.A.H.-G., T.M.S., R.K.), Department of Neurosciences, University of California, San Diego, La Jolla, California (D.E.P., A.M.D.), Multimodal Imaging Laboratory, University of California, San Diego, La Jolla, California (C.R.M., A.P.K., K.M.L., T.M.S., P.E., J.M.K., H.B., N.S.W., A.M.D., N.F.).
Background:
Diffusion-weighted imaging has shown initial promise for evaluating response to bevacizumab in patients with high-grade glioma (HGG). However, it is well recognized that the apparent diffusion coefficient (ADC) is influenced by bevacizumab-induced reductions in edema, which may limit its prognostic value. We demonstrate that an advanced diffusion-weighted imaging technique, restriction spectrum imaging (RSI), improves the evaluation of response to bevacizumab because unlike ADC, RSI is not affected by resolution of edema.
Methods:
RSI and ADC maps were analyzed for 40 patients with HGG prior to and following initiation of bevacizumab. Volumes of interest were drawn for regions of contrast enhancement (CE) and fluid attenuated inversion recovery (FLAIR) hyperintensity and histogram percentiles within volumes of interest were calculated for ADC 10th percentile (ADC-CE10%, ADC-FLAIR10%) and for RSI 90th percentile (RSI-CE90%, RSI-FLAIR90%). Cox proportional hazard models were used to evaluate the relationship between imaging parameters, progression-free survival (PFS), and overall survival (OS).
Results:
An increase in RSI-FLAIR90% following bevacizumab was the strongest predictor of poor PFS (P= .016) and OS (P= .004), whereas decreases in ADC-FLAIR10% showed a weaker association with OS only (P= .041). Within the CE region, increases in RSI-CE90% alone were associated with poorer OS. Correlational analysis revealed that decreases in FLAIR volume were associated with decreases in ADC-FLAIR10%, but not with changes in RSI-FLAIR90%.
Conclusion:
RSI is less influenced by changes in edema, conferring an advantage of RSI over ADC for evaluating response to anti-angiogenic therapy in patients with HGG.

