Carmustine Implants and O(6)-Benzylguanine in Treating Children With Recurrent Malignant Glioma

• Status: Terminated
• Trial end date: 2004-07-01
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Chemotherapy placed into the surrounding tissue after surgery to remove the tumor may kill any remaining tumor cells. O(6)-benzylguanine may increase the effectiveness of carmustine by making tumor cells more sensitive to the drug.

PURPOSE: Phase I trial to study the safety of combining O(6)-benzylguanine with carmustine implants in treating children who have recurrent malignant glioma.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Pediatric Brain Tumor Consortium
• Collaborator: National Cancer Institute (NCI)
• Treatments: Carmustine; O(6)-benzylguanine

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed progressive supratentorial anaplastic astrocytoma or glioblastoma multiforme

• No multifocal disease or leptomeningeal dissemination of tumor

• No evidence of tumor crossing midline

• Limited intraventricular involvement

• Measurable unilateral mass at least 10 mm by contrast-enhanced MRI

• Received prior involved-field radiotherapy as a component of prior therapy

• Amenable to and in need of significant debulking

PATIENT CHARACTERISTICS:

Age

• 3 to 21

Performance status

• Karnofsky 60-100% OR

• Lansky 60-100%

Life expectancy

• More than 8 weeks

Hematopoietic

• Absolute neutrophil count greater than 1,000/mm3*

• Platelet count greater than 100,000/mm3*

• Hemoglobin greater than 8 g/dL (transfusions allowed) NOTE: * Transfusion independent

Hepatic

• Bilirubin no greater than 1.5 times normal

• AST and ALT less than 3 times normal

• Albumin at least 2 g/dL

• No overt hepatic disease

Renal

• Creatinine clearance no greater than 1.5 times normal OR

• Glomerular filtration rate greater than 70 mL/min

• No overt renal disease

Cardiovascular

• No overt cardiac disease

Pulmonary

• No overt pulmonary disease

Other

• Neurological deficits must be stable for at least the past week

• No uncontrolled infection

• No known hypersensitivity to nitrosoureas or polyethylene glycol

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

• At least 6 months since prior bone marrow transplantation

• More than 2 weeks since prior colony-stimulating growth factors (e.g., filgrastim (G-CSF), sargramostim (GM-CSF), or epoetin alfa)

Chemotherapy

• No more than 2 prior cytotoxic chemotherapy regimens

• No more than 3 prior chemotherapy regimens total

• More than 3 weeks since prior myelosuppressive chemotherapy (6 weeks for nitrosoureas) and recovered

• Prior systemic carmustine (or other nitrosourea) allowed provided patient did not experience non-hematopoietic grade III/IV toxicity

Endocrine therapy

• Concurrent dexamethasone allowed if on a stable dose for at least the past week

Radiotherapy

• See Disease Characteristics

• At least 3 months since prior radiotherapy

• No prior craniospinal irradiation for metastatic disease

Surgery

• See Disease Characteristics

• Prior biopsy or cytoreductive surgery allowed

Other

• Concurrent anticonvulsants allowed

• No other concurrent anticancer or investigational drugs