| Literature DB >> 32516388 |
Jerrold L Boxerman1,2,3,4, Chad C Quarles5, Leland S Hu6,7,3, Bradley J Erickson8,7,9,3, Elizabeth R Gerstner10,11, Marion Smits12,13, Timothy J Kaufmann8,7, Daniel P Barboriak14,2,9,3, Raymond H Huang15,16, Wolfgang Wick17,13, Michael Weller18,13, Evanthia Galanis19,7, Jayashree Kalpathy-Cramer20, Lalitha Shankar21, Paula Jacobs21, Caroline Chung22,7, Martin J van den Bent23,13, Susan Chang24, W K Al Yung25, Timothy F Cloughesy26,27, Patrick Y Wen16,11, Mark R Gilbert28,29, Bruce R Rosen20, Benjamin M Ellingson26,30,11,31,2,9,3, Kathleen M Schmainda32,2.
Abstract
Despite the widespread clinical use of dynamic susceptibility contrast (DSC) MRI, DSC-MRI methodology has not been standardized, hindering its utilization for response assessment in multicenter trials. Recently, the DSC-MRI Standardization Subcommittee of the Jumpstarting Brain Tumor Drug Development Coalition issued an updated consensus DSC-MRI protocol compatible with the standardized brain tumor imaging protocol (BTIP) for high-grade gliomas that is increasingly used in the clinical setting and is the default MRI protocol for the National Clinical Trials Network. After reviewing the basis for controversy over DSC-MRI protocols, this paper provides evidence-based best practices for clinical DSC-MRI as determined by the Committee, including pulse sequence (gradient echo vs spin echo), BTIP-compliant contrast agent dosing (preload and bolus), flip angle (FA), echo time (TE), and post-processing leakage correction. In summary, full-dose preload, full-dose bolus dosing using intermediate (60°) FA and field strength-dependent TE (40-50 ms at 1.5 T, 20-35 ms at 3 T) provides overall best accuracy and precision for cerebral blood volume estimates. When single-dose contrast agent usage is desired, no-preload, full-dose bolus dosing using low FA (30°) and field strength-dependent TE provides excellent performance, with reduced contrast agent usage and elimination of potential systematic errors introduced by variations in preload dose and incubation time.Entities:
Keywords: DSC-MRI; cerebral blood volume; clinical trial; consensus protocol; high-grade glioma
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Year: 2020 PMID: 32516388 PMCID: PMC7523451 DOI: 10.1093/neuonc/noaa141
Source DB: PubMed Journal: Neuro Oncol ISSN: 1522-8517 Impact factor: 12.300