The purpose of this study is to evaluate the clinical benefit and safety of two different Dose-Intense temozolomide regimens(one-week on/one-week off regimen versus continuous dose-intense regimen)in patients with glioblastoma at first relapse.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
204
Progress-Free Survival at 6 months (PFS6)
Time frame: 6 months
Overall Survival(OS)
Time frame: 2 years
Progression free survival
Time frame: 2 years
Objective Response Rate
Time frame: up to 52 weeks
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Time frame: up to 52 weeks
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