Peritumoral ADC Values Correlate with the MGMT Methylation Status in Patients with Glioblastoma

Author:

Ladenhauf Valentin Karl12,Galijasevic Malik12ORCID,Kerschbaumer Johannes3ORCID,Freyschlag Christian Franz3ORCID,Nowosielski Martha4ORCID,Birkl-Toeglhofer Anna Maria5ORCID,Haybaeck Johannes56ORCID,Gizewski Elke Ruth12ORCID,Mangesius Stephanie12ORCID,Grams Astrid Ellen12ORCID

Affiliation:

1. Department of Neuroradiology, Medical University of Innsbruck, 6020 Innsbruck, Austria

2. Neuroimaging Research Core Facility, Medical University of Innsbruck, 6020 Innsbruck, Austria

3. Department of Neurosurgery, Medical University of Innsbruck, 6020 Innsbruck, Austria

4. Department of Neurology, Medical University of Innsbruck, 6020 Innsbruck, Austria

5. Institute of Pathology, Neuropathology and Molecular Pathology, Medical University of Innsbruck, 6020 Innsbruck, Austria

6. Diagnostic & Research Center for Molecular BioMedicine, Institute of Pathology, Medical University of Graz, 8010 Graz, Austria

Abstract

Different results have been reported concerning the relationship of the apparent diffusion coefficient (ADC) values and the status of methylation as the promoter gene for the enzyme methylguanine-DNA methyltransferase (MGMT) in patients with glioblastomas (GBs). The aim of this study was to investigate if there were correlations between the ADC values of the enhancing tumor and peritumoral areas of GBs and the MGMT methylation status. In this retrospective study, we included 42 patients with newly diagnosed unilocular GB with one MRI study prior to any treatment and histopathological data. After co-registration of ADC maps with T1-weighted sequences after contrast administration and dynamic susceptibility contrast (DSC) perfusion, we manually selected one region-of-interest (ROI) in the enhancing and perfused tumor and one ROI in the peritumoral white matter. Both ROIs were mirrored in the healthy hemisphere for normalization. In the peritumoral white matter, absolute and normalized ADC values were significantly higher in patients with MGMT-unmethylated tumors, as compared to patients with MGMT-methylated tumors (absolute values p = 0.002, normalized p = 0.0007). There were no significant differences in the enhancing tumor parts. The ADC values in the peritumoral region correlated with MGMT methylation status, confirmed by normalized ADC values. In contrast to other studies, we could not find a correlation between the ADC values or the normalized ADC values and the MGMT methylation status in the enhancing tumor parts.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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