Overview

O(6)-Benzylguanine and Carmustine in Treating Patients With Solid Tumors

Status:
Completed
Trial end date:
2004-02-01
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. Combining more than one drug may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of O(6)-benzylguanine and carmustine in treating patients who have solid tumors.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Case Comprehensive Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Carmustine
O(6)-benzylguanine
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed solid tumor for which no standard
treatment exists (including surgery, radiotherapy, or systemic agents) No primary CNS
malignancy No CNS metastases Only disease that can be sequentially biopsied is eligible for
determination of the biochemical modulating dose that decreases AGT in tumor tissue

PATIENT CHARACTERISTICS: Age: Over 18 Performance status: ECOG 0-2 Hematopoietic: WBC
greater than 4,000/mm3 Absolute neutrophil count greater than 2,000/mm3 Platelet count
greater than 100,000/mm3 Hepatic: Bilirubin less than 1.5 mg/dL AST less than 3 times
normal Prothrombin time less than upper limit of normal Renal: Creatinine no greater than
1.5 mg/dL OR Creatinine clearance at least 60 mL/min Calcium normal Electrolytes normal
Other: Diabetes controlled by diet or insulin allowed Not pregnant Fertile patients must
use effective contraception during and for 2 months after study

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: At least 4 weeks
since chemotherapy (6 weeks since mitomycin) and recovered No prior nitrosoureas Endocrine
therapy: Not specified Radiotherapy: See Disease Characteristics Surgery: Not specified