Evaluation of Gliomas with Magnetic Resonance Fingerprinting with PET Correlation—A Comparative Study

Author:

Marik Wolfgang1ORCID,Cardoso Pedro Lima2,Springer Elisabeth23,Bogner Wolfgang2,Preusser Matthias4,Widhalm Georg5ORCID,Hangel Gilbert25ORCID,Hainfellner Johannes A.6ORCID,Rausch Ivo7ORCID,Weber Michael1ORCID,Schmidbauer Victor1ORCID,Traub-Weidinger Tatjana7ORCID,Trattnig Siegfried2

Affiliation:

1. Division of Neuroradiology and Musculoskeletal Radiology, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria

2. High-Field MR Centre, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria

3. Institute of Radiology, Hietzing Hospital, 1130 Vienna, Austria

4. Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, 1090 Vienna, Austria

5. Department of Neurosurgery, Medical University of Vienna, 1090 Vienna, Austria

6. Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, 1090 Vienna, Austria

7. Division of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria

Abstract

Objectives: Advanced MR imaging of brain tumors is still mainly based on qualitative imaging. PET imaging offers additive metabolic information, and MR fingerprinting (MRF) offers a novel approach to quantitative data acquisition. The purpose of this study was to evaluate the ability of MRF to predict tumor regions and grading in combination with PET. Methods: Seventeen patients with histologically verified infiltrating gliomas and available amino-acid PET data were enrolled. ROIs for solid tumor parts (SPo), perifocal edema (ED1), and normal-appearing white matter (NAWM) were selected on conventional MRI sequences and aligned to the MRF and PET images. The predictability of gliomas by region and grading as well as intermodal correlations were assessed. Results: For MRF, we calculated an overall predictability by region (SPo, ED1, and NAWM) for all of the MRF parameters of 76.5%, 47.1%, and 94.1%, respectively. The overall ability to distinguish low- from high-grade gliomas using MRF was 88.9% for LGG and 75% for HGG, with an accuracy of 82.4%, a ppV of 85.71%, and an npV of 80%. PET positivity was found in 13/17 patients for solid tumor parts, and in 3/17 patients for the edema region. However, there was no significant difference in region-specific MRF values between PET positive and PET negative patients. Conclusions: MRF and PET provide quantitative measurements of the tumor tissue characteristics of gliomas, with good predictability. Nonetheless, the results are dissimilar, reflecting the different underlying mechanisms of each method.

Funder

Austrian Science Fund

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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