Facing Contrast-Enhancing Gliomas: Perfusion MRI in Grade III and Grade IV Gliomas according to Tumor Area

Author:

Di Stefano Anna Luisa12,Bergsland Niels3ORCID,Berzero Giulia14ORCID,Farina Lisa5,Rognone Elisa5,Gastaldi Matteo6,Aquino Domenico7ORCID,Frati Alessandro8,Tomasello Francesco9,Ceroni Mauro26,Marchioni Enrico1,Bastianello Stefano25

Affiliation:

1. Neuro-Oncology Unit, C. Mondino National Neurological Institute, 27100 Pavia, Italy

2. Department of Brain and Behavioral Sciences, University of Pavia, 27100 Pavia, Italy

3. Magnetic Resonance Laboratory, IRCCS Don Gnocchi Foundation, 20148 Milan, Italy

4. Neuroscience Consortium, University of Pavia, Monza Policlinico and Pavia Mondino, 27100 Pavia, Italy

5. Neuroradiological Department, C. Mondino National Neurological Institute, 27100 Pavia, Italy

6. General Neurology Unit, C. Mondino National Neurological Institute, 27100 Pavia, Italy

7. Department of Neuroradiology, IRCCS Foundation Neurological Institute C. Besta, 20133 Milan, Italy

8. Department of Neurosurgery, IRCCS Neuromed, Pozzilli (IS), University of Rome La Sapienza, 00185 Rome, Italy

9. Department of Neurosurgery, University of Messina, 98122 Messina, Italy

Abstract

Tumoral neoangiogenesis characterizes high grade gliomas. Relative Cerebral Blood Volume (rCBV), calculated with Dynamic Susceptibility Contrast (DSC) Perfusion-Weighted Imaging (PWI), allows for the estimation of vascular density over the tumor bed. The aim of the study was to characterize putative tumoral neoangiogenesis via the study of maximal rCBV with a Region of Interest (ROI) approach in three tumor areas—the contrast-enhancing area, the nonenhancing tumor, and the high perfusion area on CBV map—in patients affected by contrast-enhancing glioma (grades III and IV). Twenty-one patients were included: 15 were affected by grade IV and 6 by grade III glioma. Maximal rCBV values for each patient were averaged according to glioma grade. Although rCBV from contrast-enhancement and from nonenhancing tumor areas was higher in grade IV glioma than in grade III (5.58 and 2.68; 3.01 and 2.2, resp.), the differences were not significant. Instead, rCBV recorded in the high perfusion area on CBV map, independently of tumor compartment, was significantly higher in grade IV glioma than in grade III (7.51 versus 3.78,P=0.036). In conclusion, neoangiogenesis encompasses different tumor compartments and CBV maps appear capable of best characterizing the degree of neovascularization. Facing contrast-enhancing brain tumors, areas of high perfusion on CBV maps should be considered as the reference areas to be targeted for glioma grading.

Funder

National Ministry of University and Research

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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