Abstract

Purpose: To investigate the diagnostic performance of in vivo ADC-based stratification of integrated molecular glioma grades. Materials and methods: Ninety-seven patients with histopathologically confirmed glioma were evaluated retrospectively. All patients underwent pre-interventional MRI-examination including diffusion-weighted imaging (DWI) with implemented b-values of 500, 1000, 1500, 2000, and 2500 s/mm2. Apparent Diffusion Coefficient (ADC), Mean Kurtosis (MK), and Mean Diffusivity (MD) maps were generated. The average values were compared among the molecular glioma subgroups of IDH-mutant and IDH-wildtype astrocytoma, and 1p/19q-codeleted oligodendroglioma. One-way ANOVA with post-hoc Games-Howell correction compared average ADC, MD, and MK values between molecular glioma groups. A Receiver Operating Characteristic (ROC) analysis determined the area under the curve (AUC). Results: Two b-value-dependent ADC-based evaluations presented statistically significant differences between the three molecular glioma sub-groups (p < 0.001, respectively). Conclusions: High-b-value ADC from preoperative DWI may be used to stratify integrated molecular glioma subgroups and save time compared to diffusion kurtosis imaging. Higher b-values of up to 2500 s/mm2 may present an important step towards increasing diagnostic accuracy compared to standard DWI protocol.

Highlights

  • Gliomas are one of the most common primary central nervous system tumors and are, in most cases, associated with poor overall survival [1]

  • Average Apparent Diffusion Coefficient (ADC) values were significantly higher in IDH-mut gliomas than in oligodendrogliomas and IDH-wt gliomas

  • diffusionweighted imaging (DWI) may be used to stratify molecular glioma subgroups and save time compared to diffusion kurtosis imaging (DKI)

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Summary

Introduction

Gliomas are one of the most common primary central nervous system tumors and are, in most cases, associated with poor overall survival [1]. Treatment options include surgical resection, chemotherapy, and radiation therapy, depending on the histopathological entity [1,2]. The distinction between different glioma subtypes with sufficient sensitivity and specificity remains challenging in preoperative settings and imaging. A reliable pre-interventional glioma stratification based on the expected molecular glioma profile may impact therapeutic options, the extent of planned surgical resection, and prognosis [3,4,5]. Various models have been proposed in previous reports to distinguish non-invasively different tumor entities using MRI. ADC-map-based tumor evaluation from diffusionweighted imaging (DWI) seems to be a promising means of differentiation [6,7]

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