Carmustine Followed By Surgery in Treating Patients With Recurrent Supratentorial Malignant Glioma or Metastatic Brain Neoplasm
This trial is active, not recruiting.
|Conditions||brain and central nervous system tumors, metastatic cancer|
|Treatments||carmustine in ethanol, conventional surgery|
|Phase||phase 1/phase 2|
|Start date||June 2000|
|Trial identifier||NCT00009854, CDR0000068416, DTI-0002, NCI-V00-1642, UCSF-H7858-17520-01|
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.
PURPOSE: Phase I/II trial to study the effectiveness of carmustine followed by surgery in treating patients who have recurrent supratentorial malignant glioma or metastatic brain neoplasm.
|United States||No locations recruiting|
|Other countries||No locations recruiting|
Male or female participants from 18 years up to 75 years old.
DISEASE CHARACTERISTICS: - Histologically confirmed recurrent supratentorial malignant glioma with clear evidence of progression by MRI - Glioblastoma multiforme - Anaplastic ependymoma - Anaplastic astrocytoma - Anaplastic oligodendroglioma OR - Metastatic tumor to the brain other than melanoma - Planned resection of tumor (must be first surgery for recurrent disease) - Tumor volume of each tumor component or residual tumor must be at least 4 cm3 and no greater than 33.4 cm3 - Tumor shape and surrounding structure(s) unlikely to cause an irregular distribution of the injected study drug - Tumor is spherical, spheroid, or ovoid - No tumors shaped into 3 or more components (e.g., multicentric or multilobulated) - No tumors extending into the ventricular system - Tumor has an intact stroma (i.e., tumor mass not partially incised or punctured) - Central necrosis and/or central cystic areas allowed if an enhancing rim with a thickness of more than 5 mm is present - No tumors in the following locations of the brain: - Brainstem (pons or medulla) - Midbrain (mesencephalon) - Primary sensorimotor cortex in the dominant hemisphere - Within 1.5 cm of the optic chiasm, either optic nerve, or any other cranial nerve PATIENT CHARACTERISTICS: Age: - 18 to 75 Performance status: - Karnofsky 60-100% Life expectancy: - Not specified Hematopoietic: - Absolute neutrophil count at least 1,500/mm^3 - Platelet count at least 100,000/mm^3 - No evidence of bleeding diathesis Hepatic: - Bilirubin no greater than 2.0 mg/dL - SGOT and SGPT no greater than 2.5 times normal Renal: - Creatinine no greater than 2.0 mg/dL OR - Creatinine clearance at least 40 mL/min OR - BUN no greater than 30 mg/dL Other: - No active uncontrolled infection - Afebrile (37.5 degrees C) unless fever due to tumor - No other unstable or severe medical condition - No complicating medical or psychiatric problem that would preclude study - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: - Not specified Chemotherapy: - At least 4 weeks since prior systemic chemotherapy (6 weeks for nitrosoureas, mitomycin, or Gliadel wafers) and recovered - No anti-tumor chemotherapy within 12 weeks after study drug unless tumor volume increases by more than 25% by MRI Endocrine therapy: - Not specified Radiotherapy: - At least 4 weeks since prior radiotherapy and recovered - No prior intracranial brachytherapy - No anti-tumor radiotherapy within 12 weeks after study drug unless tumor volume increases by more than 25% by MRI Surgery: - See Disease Characteristics - Prior surgery allowed - No anti-tumor surgery within 12 weeks after study drug Other: - No concurrent anticoagulants - No other concurrent investigational agents
|Official title||Phase I/II Study of Intratumoral Injection of DTI-015 Prior to Tumor Resection in Patients With Recurrent Malignant Glioma or Metastatic Neoplasm to Brain|
|Description||OBJECTIVES: - Determine the extent and pattern of distribution of DNA adducts in patients with recurrent supratentorial malignant glioma or metastatic neoplasm to the brain treated with neoadjuvant intratumoral carmustine in ethanol (DTI-015) followed by tumor resection. - Determine the qualitative and quantitative toxicity of this treatment regimen in these patients. OUTLINE: This is a dose escalation study. Patients receive neoadjuvant carmustine in ethanol (DTI-015) intratumorally under stereotactic guidance 45-90 minutes prior to craniotomy and tumor resection. Cohorts of 3-6 patients receive escalating doses of DTI-015 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 3 of 3 or 3 of 6 patients experience dose-limiting toxicity. Patients are followed at 4, 8, and 12 weeks, and then every 3 months thereafter. PROJECTED ACCRUAL: A total of 15 patients will be accrued for this study.|
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