Advanced Neuroimaging in Brain Tumors : Diffusion, Spectroscopy, Perfusion and Permeability MR imaging for the evaluation of tumor characterization and surgical treatment planning.

Abstract

Advanced Neuroimaging in Brain Tumors: Diffusion, Spectroscopy, Perfusion and Permeability for the evaluation of tumor characterization and surgical treatment planning.

The current standard of neuroimaging for brain tumor evaluation is anatomy-based MRI. Unfortunately, MRI does not fully reflect the complicated biology of infiltrative glioma, and has a limited capacity to differentiate a high-grade glioma (HGG) from a single brain metastasis. Grading of gliomas is important for the determination of appropriate treatment strategies and in the assessment of prognosis. It is clinically important to distinguish HGG from a single brain metastasis, because medical staging, surgical planning, and therapeutic decisions are different for each tumor type. The basis for this thesis was 208 patients admitted at Oslo University Hospital-Ullevål with the diagnosis of brain tumor between 2006 and 2010. The aim of this thesis was to evaluate in terms of diagnostic examination performance in the clinical decision-making process the use of advanced MRI techniques, namely, diffusion-weighted imaging (DWI), magnetic resonance spectroscopic imaging (MRSI), and T2*-weighted first pass dynamic susceptibility contrast-enhanced perfusion MRI (DSC MRI) in the diagnosis and preoperative planning of brain tumors, with focus in the grading and characterization of gliomas, as well as in the assessment of the peri-enhancing region aiming to demonstrate tumor-infiltration and tumor-free edema. In this thesis, we have demonstrated that MRSI and DSC MRI can be helpful to discriminate HGG from solitary metastases, supporting the hypothesis that these advanced MRI techniques can detect infiltration of tumor cells in the peri-enhancing region. We have demonstrated that combining DWI and MRSI increases the accuracy in the determination of glioma grade. We identified differences among all glial tumor grades for the parameters cerebral blood volume (rCBV) and microvascular leakage (MVL) derived from DSC MRI. Our correlation analysis indicate that MVL, rCBV, and cerebral blood flow (rCBF) may be related to different aspects of tumor angiogeneseis.