Preoperative clinical magnetic resonance imaging (MRI) protocols for gliomas, brain tumors with dismal outcomes due to their infiltrative properties, still rely on conventional structural MRI, which does not deliver information on tumor genotype and is limited in the delineation of diffuse gliomas. The GliMR COST action wants to raise awareness about the state of the art of advanced MRI techniques in gliomas and their possible clinical translation or lack thereof. This review describes current methods, limits, and applications of advanced MRI for the preoperative assessment of glioma, summarizing the level of clinical validation of different techniques. In this first part, we discuss dynamic susceptibility contrast and dynamic contrast-enhanced MRI, arterial spin labeling, diffusion-weighted MRI, vessel imaging, and magnetic resonance fingerprinting. The second part of this review addresses magnetic resonance spectroscopy, chemical exchange saturation transfer, susceptibility-weighted imaging, MRI-PET, MR elastography, and MR-based radiomics applications. Evidence Level: 3. Technical Efficacy: Stage 2.

Hadamard time-encoded pseudo-continuous arterial spin labeling (te-pCASL) is a signal-to-noise ratio (SNR)-efficient MRI technique for acquiring dynamic pCASL signals that encodes the temporal information into the labeling according to a Hadamard matrix. In the decoding step, the contribution of each sub-bolus can be isolated resulting in dynamic perfusion scans. When acquiring te-ASL both with and without flow-crushing, the ASL-signal in the arteries can be isolated resulting in 4D-angiographic information. However, obtaining multi-timepoint perfusion and angiographic data requires two acquisitions. In this study, we propose a 3D Dense-Unet convolutional neural network with a multi-level loss function for reconstructing multi-timepoint perfusion and angiographic information from an interleaved 50 % -sampled crushed and 50 % -sampled non-crushed data, thereby negating the additional scan time. We present a framework to generate dynamic pCASL training and validation data, based on models of the intravascular and extravascular te-pCASL signals. The proposed network achieved SSIM values of 97.3 ± 1.1 and 96.2 ± 11.1 respectively for 4D perfusion and angiographic data reconstruction for 313 test data-sets.