Clinical Trials Directory

Trials / Completed

CompletedNCT00005637

Combination Chemotherapy Following Radiation Therapy in Treating Patients With Malignant Glioma

A Phase I Study of Extended Low Dose Temozolomide (SCH 52365, Temodar (R)) and Carmustine (BCNU) in the Treatment of Malignant Gliomas After Radiation Therapy

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one chemotherapy drug may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of combination chemotherapy following radiation therapy in treating patients who have malignant glioma.

Detailed description

OBJECTIVES: * Determine the safety and efficacy of extended low-dose temozolomide when combined with carmustine after radiotherapy in patients with malignant glioma. * Determine the maximum tolerated dose of this combination in this patient population. * Determine time to progression as measured from baseline gadolinium-enhanced magnetic resonance imaging in patients treated with this regimen. OUTLINE: This is a dose-escalation study of temozolomide. Patients receive oral temozolomide once daily on days 1-28 and carmustine IV over 1-3 hours beginning within 72 hours after starting temozolomide. Courses repeat every 8 weeks for up to 1 year in the absence of unacceptable toxicity or disease progression. Cohorts of 3-6 patients receive escalating doses of temozolomide until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity. Patients are followed every 2 months. PROJECTED ACCRUAL: A total of 3-24 patients will be accrued for this study within 1-2 years.

Conditions

Interventions

TypeNameDescription
DRUGcarmustine
DRUGtemozolomide

Timeline

Start date
1999-12-01
Primary completion
2003-06-01
Completion
2009-12-01
First posted
2003-01-27
Last updated
2013-04-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00005637. Inclusion in this directory is not an endorsement.