Literature DB >> 25363005

Bevacizumab: radiation combination produces restricted diffusion on brain MRI.

John R Hesselink1, Matthew J Barkovich, Tyler M Seibert, Nikdokht Farid, Karra A Muller, Kevin T Murphy, Santosh Kesari.   

Abstract

AIMS: The purpose of this paper is to investigate the effect of bevacizumab (BEV) on the diffusion properties of irradiated brain gliomas. MATERIALS &
METHODS: Neuroimaging studies and medical records of 44 patients undergoing treatment for cerebral gliomas were reviewed. MRIs were analyzed for presence of restricted diffusion, time to onset, pattern/location, duration of restriction, and persistence of restriction post-treatment with BEV.
RESULTS: Patchy confluent areas of diffusion restriction on MRI were found in 12 patients. All 12 patients received radiation therapy followed by BEV therapy. Diffusion restriction appeared 3 to 21 months after onset of radiation and 1 to 6 months after starting BEV therapy, increased in size over time, and persisted up to 23 months while on BEV. Restricted diffusion was observed in areas that received 60 Gy or more of radiation. Areas of restricted diffusion showed low T1 and increased T2 signal intensity, minimal or no contrast enhancement, and low cerebral blood volume. A thin perimeter of susceptibility outlined the restricted areas on susceptibility-weighted images in nine patients (75%). Small focal areas of tumor recurrence within larger regions of restricted diffusion were evident in only four patients (33%). In seven patients (58%) the area of restricted diffusion showed necrosis or radiation change on histology or no metabolic activity on MR spectroscopy or PET.
CONCLUSION: Restricted diffusion associated with BEV-treated cerebral gliomas occurs in regions of high-dose radiation and does not indicate high-cellularity of tumor recurrence.

Entities:  

Keywords:  MRI; bevacizumab; cerebral glioma; restricted diffusion

Mesh:

Substances:

Year:  2014        PMID: 25363005      PMCID: PMC6113949          DOI: 10.2217/cns.14.35

Source DB:  PubMed          Journal:  CNS Oncol        ISSN: 2045-0907


  19 in total

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Review 7.  Pseudoprogression and pseudoresponse in the treatment of gliomas.

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10.  Bevacizumab-induced diffusion-restricted lesions in malignant glioma patients.

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  2 in total

1.  Large-volume low apparent diffusion coefficient lesions predict poor survival in bevacizumab-treated glioblastoma patients.

Authors:  Myron Zhang; Bryanna Gulotta; Alissa Thomas; Thomas Kaley; Sasan Karimi; Igor Gavrilovic; Kaitlin M Woo; Zhigang Zhang; Julio Arevalo-Perez; Andrei I Holodny; Marc Rosenblum; Robert J Young
Journal:  Neuro Oncol       Date:  2015-11-03       Impact factor: 12.300

2.  Radiographic patterns of recurrence and pathologic correlation in malignant gliomas treated with bevacizumab.

Authors:  Alissa Thomas; Marc Rosenblum; Sasan Karimi; Lisa M DeAngelis; Antonio Omuro; Thomas J Kaley
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  2 in total

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