Velocity-Selective Arterial Spin Labeling Perfusion in Monitoring High Grade Gliomas Following Therapy: Clinical Feasibility at 1.5T and Comparison with Dynamic Susceptibility Contrast Perfusion.

arterial spin labeling (ASL) dynamic susceptibility contrast (DSC) glioblastoma glioma perfusion velocity-selective arterial spin labeling (VSASL)

Journal

Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646

Informations de publication

Date de publication:
25 Jan 2024
Historique:
received: 31 12 2023
revised: 19 01 2024
accepted: 20 01 2024
medline: 23 2 2024
pubmed: 23 2 2024
entrez: 23 2 2024
Statut: epublish

Résumé

MR perfusion imaging is important in the clinical evaluation of primary brain tumors, particularly in differentiating between true progression and treatment-induced change. The utility of velocity-selective ASL (VSASL) compared to the more commonly utilized DSC perfusion technique was assessed in routine clinical surveillance MR exams of 28 patients with high-grade gliomas at 1.5T. Using RANO criteria, patients were assigned to two groups, one with detectable residual/recurrent tumor ("RT", n = 9), and the other with no detectable residual/recurrent tumor ("NRT", n = 19). An ROI was drawn to encompass the largest dimension of the lesion with measures normalized against normal gray matter to yield rCBF and tSNR from VSASL, as well as rCBF and leakage-corrected relative CBV (lc-rCBV) from DSC. VSASL (rCBF and tSNR) and DSC (rCBF and lc-rCBV) metrics were significantly higher in the RT group than the NRT group allowing adequate discrimination (

Identifiants

pubmed: 38391701
pii: brainsci14020126
doi: 10.3390/brainsci14020126
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Institute of Health
ID : R01 HL144751, P41 EB031771

Auteurs

Sebastian Lambrecht (S)

Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.

Dapeng Liu (D)

Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.

Omar Dzaye (O)

Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

David O Kamson (DO)

Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Jonas Reis (J)

Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.

Thomas Liebig (T)

Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.

Matthias Holdhoff (M)

Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Peter Van Zijl (P)

Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.

Qin Qin (Q)

Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.

Doris D M Lin (DDM)

Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Classifications MeSH