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BRCA1 Protein Expression Predicts Survival in Glioblastoma Patients from an NRG Oncology RTOG Cohort

Authors :
Aidnag Z. Diaz
James N Atkins
Lydia Komarnicky
Jonathan P.S. Knisely
Steven P. Howard
David L. Rimm
Maria Vassilakopoulou
Jason A. Hanna
Veronique Neumeister
Edward Melian
Christopher J. Schultz
Corey J. Langer
Peixin Zhang
Michael D. Prados
Minhee Won
Adam P. Dicker
Luis Souhami
Walter J. Curran
Source :
Oncology
Publication Year :
2021
Publisher :
S. Karger AG, 2021.

Abstract

Purpose: Glioblastoma, the most common malignant brain tumor, was associated with a median survival of Methods and Materials: A TMA composed of archived glioblastoma tumors from patients treated with surgery, radiation, and non-TMZ chemother­apy, was provided by RTOG. RAD51, BRCA-1, phosphatase and tensin homolog tumor suppressor gene (PTEN), and miRNA-210 expression levels were assessed using quantitative in situ hybridization and automated quantitative protein analysis. The objectives of this analysis were to determine the association of each biomarker with overall survival (OS), using the Cox proportional hazard model. Event-time distributions were estimated using the Kaplan-Meier method and compared by the log-rank test. Results: A cohort of 66 patients was included in this study. Among the 4 biomarkers assessed, only BRCA1 expression had a statistically significant correlation with survival. From univariate analysis, patients with low BRCA1 protein expression showed a favorable outcome for OS (p = 0.04; hazard ratio = 0.56) in comparison with high expressors, with a median survival time of 18.9 versus 4.8 months. Conclusions: BRCA1 protein expression was an important survival predictor in our cohort of glioblastoma patients. This result may imply that low BRCA1 in the tumor and the consequent low level of DNA repair cause vulnerability of the cancer cells to treatment.

Details

ISSN :
14230232 and 00302414
Volume :
99
Database :
OpenAIRE
Journal :
Oncology
Accession number :
edsair.doi.dedup.....49d1a90f1ba30d263742b97c45b3b179
Full Text :
https://doi.org/10.1159/000516168