The purpose of this study is to evaluate patients with glioblastoma that is MGMT-methylated (the MGMT gene is altered by a chemical change). Patients will receive temozolomide plus radiation therapy. They will be compared to patients receiving nivolumab in addition to temozolomide plus radiation therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
716
Progression-free Survival (PFS) Determined by BICR
The time from randomization to the date of the first documented tumor progression or death by any cause. PFS will be determined by a Blinded Independent Central Review (BICR) assessed based on Radiologic Assessment in Neuro-Oncology (RANO) criteria. Specifically, RANO response criteria indicates that within the first 12 weeks of completion of radiotherapy, progression can only be assessed if the majority of the new enhancement is outside of the radiation field or if there is pathologic confirmation of progressive disease.
Time frame: From randomization to the date of the first documented tumor progression or death by any cause. (up to approximately 4.5 years)
Overall Survival (OS)
The time from the date of randomization to the date of death. who have not died by the end of the study will be censored to last known date alive. OS is assessed in the randomized population with no corticosteroids at baseline population and in the overall randomized population.
Time frame: From randomization to date of death (up to approximately 4.5 years)
Overall Survival (OS) Rates at 12 Months
Overall Survival (OS) rate is defined as the percentage of participants surviving at 12 months
Time frame: From randomization to 12 months after first dose
Overall Survival (OS) Rates at 24 Months
Overall Survival (OS) rate is defined as the percentage of participants surviving at 24 months
Time frame: From randomization to 24 months after first dose
Progression Free Survival (PFS) Based on Investigator Assessment
The time from randomization to the date of the first documented tumor progression or death by any cause. PFS will be determined by investigator assessment based Radiologic Assessment in Neuro-Oncology (RANO) criteria. Specifically, RANO response criteria indicates that within the first 12 weeks of completion of radiotherapy, progression can only be assessed if the majority of the new enhancement is outside of the radiation field or if there is pathologic confirmation of progressive disease.
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Local Institution - 0023
Birmingham, Alabama, United States
Local Institution - 0003
Phoenix, Arizona, United States
Cedars Sinai Medical Center
Los Angeles, California, United States
Local Institution - 0010
Los Angeles, California, United States
Local Institution - 0128
Sacramento, California, United States
Local Institution - 0029
San Diego, California, United States
Local Institution - 0006
San Francisco, California, United States
Local Institution - 0004
New Haven, Connecticut, United States
Local Institution - 0031
Washington D.C., District of Columbia, United States
Local Institution - 0087
Miami, Florida, United States
...and 113 more locations
Time frame: From randomization to the date of the first documented tumor progression or death by any cause. (up to approximately 4.5 years)