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Abstract #2400

Towards fully in-line single-voxel MRI spectroscopy for 2HG quantification as an IDH biomarker – can it eventually reach clinical use?

Angela Walls1,2, Benjamin Crouch1,3, Stephanie Withey4, Minh-Son To3,5, Cherie Raven3, Santosh Poonnoose5,6, Marc Agzarian3,5, and Andrew M Dwyer1,2,3,5
1Clinical and Research Imaging Centre, South Australian Health and Medical Institute, Adelaide, Australia, 2Jones Radiology, Adelaide, Australia, 3South Australian Medical Imaging, Adelaide, Australia, 4Siemens Healthcare Pty Ltd, Adelaide, Australia, 5College of Medicine & Public Health, Flinders University, Adelaide, Australia, 6Department of Neurosurgery, Flinders Medical Centre, Adelaide, Australia

Synopsis

Keywords: Tumors (Pre-Treatment), Spectroscopy

Motivation: 2HG is a biomarker of IDH-mutation status in brain gliomas and could benefit the clinic but lack of accessible acquisition and analysis approaches hamper adoption.

Goal(s): Our goal was to remove barriers to 2GH-MRS in clinical workflow through use of available sequences, feasible scan time and in-line analysis methods.

Approach: Fully blinded analysis of clinically achievable MRI spectroscopy (PRESS 97ms) data using non-clinical and vendor software was compared with histopathologic IDH status.

Results: Approach was feasible and yielded similar accuracy to previously reported edited-MRS methods. Both analyses showed acceptable ROC but inline implementation was more challenging in borderline cases and some non-glial tumours.

Impact: 2HG-MRS achieved with routinely available acquisition in clinical workflow and translated to inline analysis software could promote 2HG as a usable biomarker for IDH status in practice.

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