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Prospective genomically guided identification of "early/evolving" and "undersampled" IDH-wildtype glioblastoma leads to improved clinical outcomes.

Authors :
Zhang Y
Lucas CG
Young JS
Morshed RA
McCoy L
Oberheim Bush NA
Taylor JW
Daras M
Butowski NA
Villanueva-Meyer JE
Cha S
Wrensch M
Wiencke JK
Lee JC
Pekmezci M
Phillips JJ
Perry A
Bollen AW
Aghi MK
Theodosopoulos P
Chang EF
Hervey-Jumper SL
Berger MS
Clarke JL
Chang SM
Molinaro AM
Solomon DA
Source :
Neuro-oncology [Neuro Oncol] 2022 Oct 03; Vol. 24 (10), pp. 1749-1762.
Publication Year :
2022

Abstract

Background: Genomic profiling studies of diffuse gliomas have led to new improved classification schemes that better predict patient outcomes compared to conventional histomorphology alone. One example is the recognition that patients with IDH-wildtype diffuse astrocytic gliomas demonstrating lower-grade histologic features but genomic and/or epigenomic profile characteristic of glioblastoma typically have poor outcomes similar to patients with histologically diagnosed glioblastoma. Here we sought to determine the clinical impact of prospective genomic profiling for these IDH-wildtype diffuse astrocytic gliomas lacking high-grade histologic features but with molecular profile of glioblastoma.<br />Methods: Clinical management and outcomes were analyzed for 38 consecutive adult patients with IDH-wildtype diffuse astrocytic gliomas lacking necrosis or microvascular proliferation on histologic examination that were genomically profiled on a prospective clinical basis revealing criteria for an integrated diagnosis of "diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV" per cIMPACT-NOW criteria.<br />Results: We identified that this diagnosis consists of two divergent clinical scenarios based on integration of radiologic, histologic, and genomic features that we term "early/evolving" and "undersampled" glioblastoma, IDH-wildtype. We found that prospective genomically guided identification of early/evolving and undersampled IDH-wildtype glioblastoma resulted in more aggressive patient management and improved clinical outcomes compared to a biologically matched historical control patient cohort receiving standard-of-care therapy based on histomorphologic diagnosis alone.<br />Conclusions: These results support routine use of genomic and/or epigenomic profiling to accurately classify glial neoplasms, as these assays not only improve diagnostic classification but critically lead to more appropriate patient management that can improve clinical outcomes.<br /> (© The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.)

Details

Language :
English
ISSN :
1523-5866
Volume :
24
Issue :
10
Database :
MEDLINE
Journal :
Neuro-oncology
Publication Type :
Academic Journal
Accession number :
35395677
Full Text :
https://doi.org/10.1093/neuonc/noac089