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Prospective biomarker study in newly diagnosed glioblastoma: Cyto-C clinical trial.

Authors :
Griguer CE
Oliva CR
Coffey CS
Cudkowicz ME
Conwit RA
Gudjonsdottir AL
Ecklund DJ
Fedler JK
Neill-Hudson TM
Nabors LB
Benge M
Hackney JR
Chase M
Leonard TP
Patel T
Colman H
de la Fuente M
Chaudhary R
Marder K
Kreisl T
Mohile N
Chheda MG
McNeill K
Kumthekar P
Dogan A
Drappatz J
Puduvalli V
Kowalska A
Graber J
Gerstner E
Clark S
Salacz M
Markert J
Source :
Neuro-oncology advances [Neurooncol Adv] 2021 Dec 24; Vol. 4 (1), pp. vdab186. Date of Electronic Publication: 2021 Dec 24 (Print Publication: 2022).
Publication Year :
2021

Abstract

Background: Glioblastoma (GBM) has a 5-year survival rate of 3%-5%. GBM treatment includes maximal resection followed by radiotherapy with concomitant and adjuvant temozolomide (TMZ). Cytochrome C oxidase (CcO) is a mitochondrial enzyme involved in the mechanism of resistance to TMZ. In a prior retrospective trial, CcO activity in GBMs inversely correlated with clinical outcome. The current Cyto-C study was designed to prospectively evaluate and validate the prognostic value of tumor CcO activity in patients with newly diagnosed primary GBM, and compared to the known prognostic value of MGMT promoter methylation status.<br />Methods: This multi-institutional, blinded, prospective biomarker study enrolled 152 patients with newly diagnosed GBM who were to undergo surgical resection and would be candidates for standard of care. The primary end point was overall survival (OS) time, and the secondary end point was progression-free survival (PFS) time. Tumor CcO activity and MGMT promoter methylation status were assayed in a centralized laboratory.<br />Results: OS and PFS did not differ by high or low tumor CcO activity, and the prognostic validity of MGMT promoter methylation was confirmed. Notably, a planned exploratory analysis suggested that the combination of low CcO activity and MGMT promoter methylation in tumors may be predictive of long-term survival.<br />Conclusions: Tumor CcO activity alone was not confirmed as a prognostic marker in GBM patients. However, the combination of low CcO activity and methylated MGMT promoter may reveal a subgroup of GBM patients with improved long-term survival that warrants further evaluation. Our work also demonstrates the importance of performing large, multi-institutional, prospective studies to validate biomarkers. We also discuss lessons learned in assembling such studies.<br /> (© The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.)

Details

Language :
English
ISSN :
2632-2498
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
Neuro-oncology advances
Publication Type :
Academic Journal
Accession number :
35088051
Full Text :
https://doi.org/10.1093/noajnl/vdab186