Clinical trial · Interventional
Bevacizumab and Carmustine in Treating Patients With Relapsed or Progressive High-Grade Glioma
Phase II Study of Bevacizumab (Avastin) and BCNU for Treatment of Relapsed, High Grade Gliomas
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as carmustine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving bevacizumab together with carmustine may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving bevacizumab together with carmustine works in treating patients with relapsed or progressive high-grade glioma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Glioma | Glioma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| bevacizumab | Drug | Bevacizumab | ALIAS |
| carmustine | Drug | Carmustine | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Bevacizumab and Carmustine
- interventionNames
- Drug: bevacizumab
- Drug: carmustine
Primary outcomes (1)
- measure
- Progression-free Survival
- timeFrame
- Time from first day of treatment to the first observation of disease progression or death due to any cause (up to 7 years).
- description
- Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.
Secondary outcomes (4)
- measure
- Radiographic Response to Therapy
- timeFrame
- One year
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically confirmed GBM, anaplastic astrocytoma, anaplastic oligoastrocytoma or anaplastic oligodendroglioma. * Disease progression (confirmed by MRI, PET or both) after radiation therapy * At least 28 days have elapsed since chemotherapy, major surgery or radiation therapy. * No other malignancy within 3 years except for non-melanomatous skin cancer or in situ cervical cancer. * Karnofsky performance score at least 70 * Platelet count ≥ 130/mm3. * Absolute neutrophil count ≥ 1500/mm3 * Calculated creatinine clearance greater than 45 mg/dl * AST \< 2 times the upper limit of normal * Bilirubin \< 1.5 times the upper limit of normal * Ability to give signed informed consent * Patients must be 18 years of age or older. Exclusion Criteria: * Prior intravenous or oral nitrosoureas (BCNU, CCNU) or prior VEGF targeted therapy including bevacizumab. No more than two prior chemotherapy regimens are allowed. Prior or current steroid use is allowed. * Evidence of CNS hemorrhage * Requirement for therapeutic anticoagulation * Any grade 3 or greater hemorrhage within the previous 28 days * Active inflammatory bowel disease * Inadequately controlled hypertension * Any prior history of hypertensive crisis or hypertensive encephalopathy * New York Heart Association Grade II or greater congestive heart failure * History of myocardial infarction or unstable angina within 6 months prior to study enrollment * History of stroke or transient ischemic attack within 6 months prior to study enrollment * Significant vascular disease * Symptomatic peripheral vascular disease * Evidence of bleeding diathesis or coagulopathy * Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to study enrollment or anticipation of need for major surgical procedure during the course of the study * Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to study enrollment * History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to study enrollment * Serious, non-healing wound, ulcer, or bone fracture * Proteinuria at screening * Pregnant (or lactating). Use of effective means of contraception in subjects of child-bearing potential * Prior organ transplantation * Known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies * Known acquired immune deficiency syndrome (AIDS) or HIV positive status
References
Publications (0)
Data not yet available