The methylation status of the MGMT promoter has been identified as a strong and independent predictive factor of favorable survival in glioblastoma patients undergoing chemotherapy with alkylating agents
MGMT and CDKN2A status subdivided a cohort into three race-specific groups with different prognoses. This findings indicate that bevacizumab (BEV) approval in Japan led to overall survival (OS) improvement exclusively for patients with concurrent unmethylated MGMT promoter status and CDKN2A homozygous deletion 1)