Prospective comparative diagnostic accuracy evaluation of dynamic contrast-enhanced (DCE) vs. dynamic susceptibility contrast (DSC) MR perfusion in differentiating tumor recurrence from radiation necrosis in treated high-grade gliomas.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
08 2019
Historique:
received: 12 09 2018
revised: 04 12 2018
accepted: 05 12 2018
pubmed: 8 1 2019
medline: 22 9 2020
entrez: 8 1 2019
Statut: ppublish

Résumé

The appearance of a new enhancing lesion after surgery and chemoradiation for high-grade glioma (HGG) presents a common diagnostic dilemma. Histopathological analysis remains the reference standard in this situation. To prospectively compare the diagnostic accuracy of dynamic contrast-enhanced (DCE) vs. dynamic susceptibility contrast (DSC) in differentiating tumor recurrence (TR) from radiation necrosis (RN). Prospective diagnostic accuracy study. In all, 98 consecutive treated HGG patients with new enhancing lesion. We excluded 32 patients due to inadequate follow-up or technical limitation. 3 T DCE and DSC MR. Histogram and hot-spot analysis of cerebral blood volume (CBV), corrected CBV, K Mann-Whitney U-tests, receiver operating characteristic (ROC) curve, and logistic regression analysis. A total of 68 lesions were included. There were 37 TR, 28 RN, and three lesions with equal proportions of TR and RN. TR had significantly higher CBV, corrected CBV, CBV ratio, corrected CBV ratio, AUC ratio, and Vp ratio (P < 0.05) than RN on hot-spot analysis. CBV had the highest diagnostic accuracy (AUROC 0.71). On histogram analysis, TR had higher CBV and corrected CBV maximal value compared with RN (P = 0.006, AUROC = 0.70). Only CBV on hot-spot analysis remained significant after correction for multiple comparison, with no significant improvement in diagnostic accuracy when using a combination of parameters (AUROC 0.71 vs. 0.76, P = 0.24). DSC-derived CBV is the most accurate perfusion parameter in differentiating TR and RN. DSC and DCE-derived parameters reflecting the blood volume in an enhancing lesion are more accurate than the DCE-derived parameter K 1 Technical Efficacy Stage: 4 J. Magn. Reson. Imaging 2019;50:573-582.

Sections du résumé

BACKGROUND
The appearance of a new enhancing lesion after surgery and chemoradiation for high-grade glioma (HGG) presents a common diagnostic dilemma. Histopathological analysis remains the reference standard in this situation.
PURPOSE
To prospectively compare the diagnostic accuracy of dynamic contrast-enhanced (DCE) vs. dynamic susceptibility contrast (DSC) in differentiating tumor recurrence (TR) from radiation necrosis (RN).
STUDY TYPE
Prospective diagnostic accuracy study.
POPULATION
In all, 98 consecutive treated HGG patients with new enhancing lesion. We excluded 32 patients due to inadequate follow-up or technical limitation.
FIELD STRENGTH/SEQUENCE
3 T DCE and DSC MR.
ASSESSMENT
Histogram and hot-spot analysis of cerebral blood volume (CBV), corrected CBV, K
STATISTICAL TESTS
Mann-Whitney U-tests, receiver operating characteristic (ROC) curve, and logistic regression analysis.
RESULTS
A total of 68 lesions were included. There were 37 TR, 28 RN, and three lesions with equal proportions of TR and RN. TR had significantly higher CBV, corrected CBV, CBV ratio, corrected CBV ratio, AUC ratio, and Vp ratio (P < 0.05) than RN on hot-spot analysis. CBV had the highest diagnostic accuracy (AUROC 0.71). On histogram analysis, TR had higher CBV and corrected CBV maximal value compared with RN (P = 0.006, AUROC = 0.70). Only CBV on hot-spot analysis remained significant after correction for multiple comparison, with no significant improvement in diagnostic accuracy when using a combination of parameters (AUROC 0.71 vs. 0.76, P = 0.24).
DATA CONCLUSION
DSC-derived CBV is the most accurate perfusion parameter in differentiating TR and RN. DSC and DCE-derived parameters reflecting the blood volume in an enhancing lesion are more accurate than the DCE-derived parameter K
LEVEL OF EVIDENCE
1 Technical Efficacy Stage: 4 J. Magn. Reson. Imaging 2019;50:573-582.

Identifiants

pubmed: 30614146
doi: 10.1002/jmri.26621
doi:

Substances chimiques

Contrast Media 0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

573-582

Informations de copyright

© 2019 International Society for Magnetic Resonance in Medicine.

Auteurs

Nader Zakhari (N)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

Michael S Taccone (MS)

University of Ottawa, Ottawa, Ontario, Canada.
Laboratory Medicine & Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Carlos H Torres (CH)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

Santanu Chakraborty (S)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

John Sinclair (J)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

John Woulfe (J)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

Gerard H Jansen (GH)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

Greg O Cron (GO)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.
Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Rebecca E Thornhill (RE)

Ottawa Hospital, Ottawa, Ontario, Canada.

Matthew D F McInnes (MDF)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.
Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Thanh B Nguyen (TB)

University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital, Ottawa, Ontario, Canada.

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