Dataset Information

Multiparametric MR-PET measurements in hypermetabolic regions reflect differences in molecular status and tumor grade in treatment-naive diffuse gliomas.

ABSTRACT:

Purpose

To assess whether hypermetabolically-defined regions of interest (ROIs) on 3,4-dihydroxy-6-[18F]-fluoro-L-phenylalanine (FDOPA) positron emission tomography (PET) could be used to evaluate physiological features and whether there are measurable differences between molecular subtypes and tumor grades.

Methods

Sixty-eight treatment-naïve glioma patients who underwent FDOPA PET and magnetic resonance imaging (MRI) were retrospectively included. Fluid-attenuated inversion recovery hyperintense regions (FLAIR_ROI) were segmented. FDOPA hypermetabolic regions (FDOPA_ROI, tumor-to-striatum ratios > 1) within FLAIR_ROI were extracted. Normalized maximum standardized uptake value (nSUV_max), volume of each ROI, and median relative cerebral blood volume (rCBV) and apparent diffusion coefficient (ADC) within FLAIR_ROI or FDOPA_ROI were calculated. Imaging metrics were compared using Students t or Mann-Whitney U tests. Area under the curve (AUC) of receiver-operating characteristic curves were used to determine whether imaging metrics within FLAIR_ROI or FDOPA_ROI can discriminate different molecular statuses or grades.

Results

Using either FLAIR_ROI or FDOPA_ROI, the nSUV_max and rCBV were significantly higher and the ADC was lower in isocitrate dehydrogenase (IDH) wild-type than mutant gliomas, and in higher-grade gliomas (HGGs) than lower-grade gliomas (LGGs). The FDOPA_ROI volume was significantly higher in 1p19q codeleted than non-codeleted gliomas, and in HGGs than LGGs. Although not significant, imaging metrics extracted by FDOPA_ROI discriminated molecular status and tumor grade more accurately than those extracted by FLAIR_ROI (AUC of IDH status, 0.87 vs. 0.82; 1p19q status, 0.78 vs. 0.73; grade, 0.87 vs. 0.76).

Conclusion

FDOPA hypermetabolic ROI may extract useful imaging features of gliomas, which can illuminate biological differences between different molecular status or tumor grades.

SUBMITTER: Tatekawa H

PROVIDER: S-EPMC7682113 | biostudies-literature |

REPOSITORIES: biostudies-literature

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