A Study to Evaluate Bevacizumab Alone or in Combination With Irinotecan for Treatment of Glioblastoma Multiforme (BRAIN)

Glioblastoma Clinical Trial

— BRAIN  

Official title:

A Phase II, Multicenter, Randomized, Non-Comparative Clinical Trial to Evaluate the Efficacy and Safety of Bevacizumab Alone or in Combination With Irinotecan for Treatment of Glioblastoma Multiforme in First or Second Relapse

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00345163
• Other study ID #: AVF3708g
• Status: Completed
• Phase: Phase 2
• First received: June 23, 2006
• Last updated: May 15, 2017
• Start date: July 2006
• Est. completion date: September 2007

Study information

• Verified date: May 2017
• Source: Genentech, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase II, open-label, multicenter, randomized, non comparative study consisting of two concurrent single-arms. Approximately 160 subjects will be randomized in a 1:1 ratio to Arm 1 (bevacizumab alone) or Arm 2 (bevacizumab + irinotecan).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 167
• Est. completion date: September 2007
• Est. primary completion date: September 2007
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed Informed Consent Form

• Age = 18 years

• Histologically confirmed GBM in first or second relapse

• Radiographic demonstration of disease progression following prior therapy

• Bi-dimensionally measurable disease with a minimum measurement of 1 cm (10 mm) in one diameter on MRI performed within 14 days prior to first treatment (Day 0)

• An interval of = 4 weeks since prior surgical resection

• Prior standard radiation for GBM

• Prior chemotherapy: first-relapse subjects

• Prior chemotherapy: second-relapse subjects

• Recovery from the effects of prior therapy, including the following: 4 weeks from cytotoxic agents (except 6 weeks from nitrosoureas, 3 weeks from procarbazine, 2 weeks from vincristine); 4 weeks from any investigational agent; 1 week from non-cytotoxic agents; 8 weeks from radiotherapy to minimize the potential for MRI changes related to radiation necrosis that might be misdiagnosed as progression of disease, or 4 weeks if a new lesion, relative to the pre-radiation MRI, develops that is outside the primary radiation field

• Prior therapy with gamma knife or other focal high-dose radiation is allowed but the subject must have subsequent histologic documentation of recurrence, unless the recurrence is a new lesion outside the irradiated field

• Karnofsky performance status = 70

• Life expectancy > 12 weeks

• Use of an effective means of contraception in males and in females of childbearing potential

• Ability to comply with study and follow-up procedures

Exclusion Criteria:

• Prior treatment with irinotecan, bevacizumab, or another VEGF or VEGFR-targeted agent

• Prior treatment with prolifeprospan 20 with carmustine wafer

• Prior intracerebral agents

• Need for urgent palliative intervention for primary disease (e.g., impending herniation)

• Evidence of recent hemorrhage on baseline MRI of the brain with the following exceptions: Presence of hemosiderin; Resolving hemorrhagic changes related to surgery; Presence of punctate hemorrhage in the tumor

• Received more than two treatment regimens for Grade III and/or Grade IV glioma

• Blood pressure of > 150 mmHg systolic and > 100 mmHg diastolic

• History of hypertensive encephalopathy

• New York Heart Association (NYHA) Grade II or greater CHF

• History of myocardial infarction or unstable angina within 6 months prior to Day 0

• History of stroke or transient ischemic attack within 6 months prior to study enrollment

• Significant vascular disease (e.g., aortic aneurysm, aortic dissection) or recent peripheral arterial thrombosis within 6 months prior to Day 0

• Evidence of bleeding diathesis or coagulopathy

• History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day 0

• History of intracerebral abscess within 6 months prior to Day 0

• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, anticipation of need for major surgical procedure during the course of the study

• Minor surgical procedures (excluding placement of a vascular access device), stereotactic biopsy, fine needle aspirations, or core biopsies within 7 days prior to Day 0

• Serious non-healing wound, ulcer, or bone fracture

• Pregnancy (positive pregnancy test) or lactation

• Known hypersensitivity to any component of bevacizumab

• History of any other malignancy within 5 years (except non-melanoma skin cancer or carcinoma in situ of the cervix)

• Pregnant or nursing females

• Unstable systemic disease, including active infection, uncontrolled hypertension, or serious cardiac arrhythmia requiring medication

• Subjects unable to undergo an MRI with contrast

Related Conditions & MeSH terms

• Glioblastoma

Intervention

Drug:
• bevacizumab
Intravenous repeating dose
• irinotecan
Intravenous repeating dose

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Genentech, Inc.

References & Publications (1)

Friedman HS, Prados MD, Wen PY, Mikkelsen T, Schiff D, Abrey LE, Yung WK, Paleologos N, Nicholas MK, Jensen R, Vredenburgh J, Huang J, Zheng M, Cloughesy T. Bevacizumab alone and in combination with irinotecan in recurrent glioblastoma. J Clin Oncol. 2009 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective response, as determined by the independent review facility (IRF)		Complete response or partial response, determined on two consecutive assessments =4 weeks apart
Primary	Progression-free survival, as determined by the IRF		6 months
Secondary	Incidence of adverse events and serious adverse events		Length of patient on study
Secondary	Duration of objective response, as determined by the IRF		Complete or partial response determined on two consecutive assessments =4 weeks apart
Secondary	Overall survival		Time from randomization to death