A Study of Bevacizumab (Avastin®) in Combination With Temozolomide and Radiotherapy in Participants With Newly Diagnosed Glioblastoma



Status:Completed
Conditions:Brain Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:9/27/2017
Start Date:June 29, 2009
End Date:September 9, 2015

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A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase III Trial of Bevacizumab, Temozolomide and Radiotherapy, Followed by Bevacizumab and Temozolomide Versus Placebo, Temozolomide and Radiotherapy Followed by Placebo and Temozolomide in Patients With Newly Diagnosed Glioblastoma

This 2 arm study investigated the efficacy and safety of the addition of bevacizumab to the
current standard of care (multimodality therapy of concurrent radiotherapy plus temozolomide
followed by adjuvant temozolomide) as compared to the current standard of care alone.
Participants were randomly assigned to either the bevacizumab (10 milligrams per kilogram
(mg/kg) intravenously [IV] once every 2 week [q2w]) or the placebo arm, in combination with
radiation therapy (total dose 60 Gray [Gy], administered as 2 Gy fractions, 5 days/week) plus
temozolomide (75 milligrams per meter squared [mg/m^2] oral administration [po] daily) for 6
weeks. After a 4 week treatment break, participants continued to receive bevacizumab (10
mg/kg IV q2w) or placebo, plus temozolomide (150-200 mg/m^2 po daily on days 1-5 of each 4
week cycle) for 6 cycles of maintenance treatment or until disease progression or
unacceptable toxicity, whichever occured first. Following the maintenance phase, bevacizumab
(15 mg/kg iv every 3 weeks [q3w]) or placebo monotherapy continued. The time on study
treatment was until disease progression.


Key Inclusion Criteria:

- newly diagnosed glioblastoma

- World Health Organization (WHO) performance status less than or equal to (<=2)

- stable or decreasing corticosteroid dose within 5 days prior to randomization

Key Exclusion Criteria:

- evidence of recent hemorrhage on postoperative magnetic resonance imaging (MRI) of
brain

- any prior chemotherapy or immunotherapy for glioblastomas and low grade astrocytomas

- any prior radiotherapy to brain

- clinically significant cardiovascular disease

- history of greater than or equal to (>=) grade 2 hemoptysis within 1 month prior to
randomization

- previous centralized screening for Methylguanine-DNA methyltransferase (MGMT) status
for enrollment into a clinical trial
We found this trial at
10
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Aurora, Colorado 80045
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510 20th Street South
Birmingham, Alabama 35294
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Charlottesville, Virginia 22903
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Cincinnati, Ohio 45220
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Cincinnati, OH
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Detroit, Michigan 48202
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2650 Ridge Avenue
Evanston, Illinois 60201
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Evanston, IL
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Los Angeles, California 90095
(310) 825-4321
UCLA UCLA's primary purpose as a public research university is the creation, dissemination, preservation and...
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250 25th Avenue North
Nashville, Tennessee 37203
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Nashville, TN
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Randwick,
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Tampa, Florida 33612
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Tampa, FL
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