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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.
Lambrecht, Sebastian; Liu, Dapeng; Dzaye, Omar; Kamson, David O; Reis, Jonas; Liebig, Thomas; Holdhoff, Matthias; Van Zijl, Peter; Qin, Qin; Lin, Doris D M.
Afiliação
  • Lambrecht S; Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Liu D; Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.
  • Dzaye O; Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Kamson DO; F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
  • Reis J; Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Liebig T; Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Holdhoff M; Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.
  • Van Zijl P; Institute of Neuroradiology, University Hospital LMU Munich, 81377 Munich, Germany.
  • Qin Q; Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Lin DDM; Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Brain Sci ; 14(2)2024 Jan 25.
Article em En | MEDLINE | ID: mdl-38391701
ABSTRACT
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 (p < 0.05, Mann-Whitney test). Lin's concordance analyses showed moderate to excellent concordance between the two methods, with a stronger, moderate correlation between VSASL rCBF and DSC lc-rCBV (r = 0.57, p = 0.002; Pearson's correlation). These results suggest that VSASL is clinically feasible at 1.5T and has the potential to offer a noninvasive alternative to DSC perfusion in monitoring high-grade gliomas following therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Brain Sci Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Brain Sci Ano de publicação: 2024 Tipo de documento: Article