Diagnostic Accuracy of Arterial Spin-Labeling, Dynamic Contrast-Enhanced, and DSC Perfusion Imaging in the Diagnosis of Recurrent High-Grade Gliomas: A Prospective Study.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
02 2023
Historique:
received: 28 07 2022
accepted: 30 12 2022
pmc-release: 01 02 2024
pubmed: 27 1 2023
medline: 4 2 2023
entrez: 26 1 2023
Statut: ppublish

Résumé

For patients with high-grade gliomas, the appearance of a new, enhancing lesion after surgery and chemoradiation represents a diagnostic dilemma. We hypothesized that MR perfusion without and with contrast can differentiate tumor recurrence from radiation necrosis. In this prospective study, we performed 3 MR perfusion methods: arterial spin-labeling, DSC, and dynamic contrast enhancement. For each lesion, we measured CBF from arterial spin-labeling, uncorrected relative CBV, and leakage-corrected relative CBV from DSC imaging. The volume transfer constant and plasma volume were obtained from dynamic contrast-enhanced imaging without and with T1 mapping using modified Look-Locker inversion recovery (MOLLI). The diagnosis of tumor recurrence or radiation necrosis was determined by either histopathology for patients who underwent re-resection or radiologic follow-up for patients who did not have re-resection. There were 26 patients with 32 lesions, 19 lesions with tumor recurrence and 13 lesions with radiation necrosis. Compared with radiation necrosis, lesions with tumor recurrence had higher CBF ( In the differentiation of tumor recurrence from radiation necrosis in a newly enhancing lesion, the diagnostic value of arterial spin-labeling-derived CBF is similar to that of DSC and dynamic contrast-enhancement-derived blood volume.

Sections du résumé

BACKGROUND AND PURPOSE
For patients with high-grade gliomas, the appearance of a new, enhancing lesion after surgery and chemoradiation represents a diagnostic dilemma. We hypothesized that MR perfusion without and with contrast can differentiate tumor recurrence from radiation necrosis.
MATERIALS AND METHODS
In this prospective study, we performed 3 MR perfusion methods: arterial spin-labeling, DSC, and dynamic contrast enhancement. For each lesion, we measured CBF from arterial spin-labeling, uncorrected relative CBV, and leakage-corrected relative CBV from DSC imaging. The volume transfer constant and plasma volume were obtained from dynamic contrast-enhanced imaging without and with T1 mapping using modified Look-Locker inversion recovery (MOLLI). The diagnosis of tumor recurrence or radiation necrosis was determined by either histopathology for patients who underwent re-resection or radiologic follow-up for patients who did not have re-resection.
RESULTS
There were 26 patients with 32 lesions, 19 lesions with tumor recurrence and 13 lesions with radiation necrosis. Compared with radiation necrosis, lesions with tumor recurrence had higher CBF (
CONCLUSIONS
In the differentiation of tumor recurrence from radiation necrosis in a newly enhancing lesion, the diagnostic value of arterial spin-labeling-derived CBF is similar to that of DSC and dynamic contrast-enhancement-derived blood volume.

Identifiants

pubmed: 36702501
pii: ajnr.A7771
doi: 10.3174/ajnr.A7771
pmc: PMC9891339
doi:

Substances chimiques

Spin Labels 0
Contrast Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

134-142

Informations de copyright

© 2023 by American Journal of Neuroradiology.

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Auteurs

T B Nguyen (TB)

From the Department of Radiology (T.B.N., N.Z., R.T.), Radiation Oncology and Medical Physics thnguyen@toh.ca.
University of Ottawa (T.B.N., N.Z., J.W., G.J., R.T.), Ottawa, Ontario, Canada.
The Ottawa Hospital Research Institute (T.B.N., J.W., G.J., R.T.), Ottawa, Ontario, Canada.

N Zakhari (N)

From the Department of Radiology (T.B.N., N.Z., R.T.), Radiation Oncology and Medical Physics.
University of Ottawa (T.B.N., N.Z., J.W., G.J., R.T.), Ottawa, Ontario, Canada.

S Velasco Sandoval (S)

Division of Neuroradiology (S.V.S., A.G.-C.), Department of Radiology, Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, D.C., Colombia.

A Guarnizo-Capera (A)

Division of Neuroradiology (S.V.S., A.G.-C.), Department of Radiology, Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, D.C., Colombia.

M Alexios Gulak (M)

Department of Anesthesiology and Pain Medicine (M.A.G.), University of Toronto, Toronto, Ontario, Canada.

J Woulfe (J)

Department of Pathology and Laboratory Medicine (J.W., G.J.), The Ottawa Hospital, Ottawa, Ontario, Canada.
University of Ottawa (T.B.N., N.Z., J.W., G.J., R.T.), Ottawa, Ontario, Canada.
The Ottawa Hospital Research Institute (T.B.N., J.W., G.J., R.T.), Ottawa, Ontario, Canada.

G Jansen (G)

Department of Pathology and Laboratory Medicine (J.W., G.J.), The Ottawa Hospital, Ottawa, Ontario, Canada.
University of Ottawa (T.B.N., N.Z., J.W., G.J., R.T.), Ottawa, Ontario, Canada.
The Ottawa Hospital Research Institute (T.B.N., J.W., G.J., R.T.), Ottawa, Ontario, Canada.

R Thornhill (R)

From the Department of Radiology (T.B.N., N.Z., R.T.), Radiation Oncology and Medical Physics.
University of Ottawa (T.B.N., N.Z., J.W., G.J., R.T.), Ottawa, Ontario, Canada.
The Ottawa Hospital Research Institute (T.B.N., J.W., G.J., R.T.), Ottawa, Ontario, Canada.

N Majtenyi (N)

Department of Medical Physics (N.M.), Grand River Regional Cancer Centre, Kitchener, Ontario, Canada.

G O Cron (GO)

Stanford University (G.O.C.), Stanford, California.

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