Literature DB >> 21856685

Graded functional diffusion map-defined characteristics of apparent diffusion coefficients predict overall survival in recurrent glioblastoma treated with bevacizumab.

Benjamin M Ellingson1, Timothy F Cloughesy, Albert Lai, Paul S Mischel, Phioanh L Nghiemphu, Shadi Lalezari, Kathleen M Schmainda, Whitney B Pope.   

Abstract

Diffusion imaging has shown promise as a predictive and prognostic biomarker in glioma. We assessed the ability of graded functional diffusion maps (fDMs) and apparent diffusion coefficient (ADC) characteristics to predict overall survival (OS) in recurrent glioblastoma multiforme (GBM) patients treated with bevacizumab. Seventy-seven patients with recurrent GBMs were retrospectively examined. MRI scans were obtained before and approximately 6 weeks after treatment with bevacizumab. Graded fDMs were created by registering datasets to each patient's pretreatment scan and then performing voxel-wise subtraction between post- and pretreatment ADC maps. Voxels were categorized according to the degree of change in ADC within pretreatment fluid-attenuated inversion recovery (FLAIR) and contrast-enhancing regions of interest (ROIs). We found that the volume of tissue showing decreased ADC within both FLAIR and contrast-enhancing regions stratified OS (log-rank, P < .05). fDMs applied to contrast-enhancing ROIs more accurately predicted OS compared with fDMs applied to FLAIR ROIs. Graded fDMs (showing voxels with decreased ADC between 0.25 and 0.4 µm(2)/ms) were more predictive of OS than traditional (single threshold) fDMs, and the predictive ability of graded fDMs could be enhanced even further by adding the ADC characteristics from the fDM-classified voxels to the analysis (log-rank, P < .001). These results demonstrate that spatially resolved diffusion-based tumor metrics are a powerful imaging biomarker of survival in patients with recurrent GBM treated with bevacizumab.

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Year:  2011        PMID: 21856685      PMCID: PMC3177656          DOI: 10.1093/neuonc/nor079

Source DB:  PubMed          Journal:  Neuro Oncol        ISSN: 1522-8517            Impact factor:   12.300


  31 in total

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Authors:  Benjamin M Ellingson; Mark G Malkin; Scott D Rand; Jennifer M Connelly; Carolyn Quinsey; Pete S LaViolette; Devyani P Bedekar; Kathleen M Schmainda
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5.  Outcomes and prognostic factors in recurrent glioma patients enrolled onto phase II clinical trials.

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9.  Utility of functional diffusion maps to monitor a patient diagnosed with gliomatosis cerebri.

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Review 10.  Molecular mechanisms of developmental and tumor angiogenesis.

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  43 in total

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Journal:  Neuro Oncol       Date:  2015-09-12       Impact factor: 12.300

2.  Persistent diffusion-restricted lesions in bevacizumab-treated malignant gliomas are associated with improved survival compared with matched controls.

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3.  pH-weighted amine chemical exchange saturation transfer echoplanar imaging (CEST-EPI) as a potential early biomarker for bevacizumab failure in recurrent glioblastoma.

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Journal:  Eur Radiol       Date:  2019-02-26       Impact factor: 5.315

Review 5.  An Update on the Approach to the Imaging of Brain Tumors.

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9.  Histogram analysis of apparent diffusion coefficient within enhancing and nonenhancing tumor volumes in recurrent glioblastoma patients treated with bevacizumab.

Authors:  Rifaquat Rahman; Alhafidz Hamdan; Rebecca Zweifler; Han Jiang; Andrew D Norden; David A Reardon; Srinivasan Mukundan; Patrick Y Wen; Raymond Y Huang
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10.  Choline-to-N-acetyl aspartate and lipids-lactate-to-creatine ratios together with age assemble a significant Cox's proportional-hazards regression model for prediction of survival in high-grade gliomas.

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Journal:  Br J Radiol       Date:  2016-09-14       Impact factor: 3.039

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