Overview

Bryostatin 1 in Treating Patients With Myelodysplastic Syndrome

Status:
Completed
Trial end date:
2003-06-01
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. PURPOSE: Phase II trial to study the effectiveness of bryostatin 1 in treating patients with myelodysplastic syndrome.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Barbara Ann Karmanos Cancer Institute
Collaborator:
National Cancer Institute (NCI)
Treatments:
Bryostatin 1
Criteria
DISEASE CHARACTERISTICS: Histologically diagnosed refractory anemia, refractory anemia with
excess blasts, refractory anemia with excess blasts in transformation, refractory anemia
with ringed sideroblasts, or chronic myelomonocytic leukemia with significant cytopenias of
at least 4 weeks duration No more than 1 prior treatment for disease Not eligible for
allogeneic bone marrow transplantation if less than 60 years of age

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Zubrod 0-2 Life expectancy:
At least 12 weeks Hematopoietic: Hematocrit less than 26% (or requiring transfusion) for at
least 4 weeks Absolute neutrophil count less than 1000/mm3 for at least 4 weeks Platelet
count less than 50/mm3 for at least 4 weeks Hepatic: Bilirubin less than 1.5 mg/dL
Transaminase less than 2.5 times upper limit of normal Renal: Creatinine less than 1.5
mg/dL Creatinine clearance of at least 60 mL/min Other: Not pregnant or lactating Fertile
patients must use effective contraception while on study and for 100 days afterwards No
uncontrolled or life-threatening infection

PRIOR CONCURRENT THERAPY: Biologic therapy: No concurrent immunotherapy No concurrent
treatment with growth factors Chemotherapy: At least 4 weeks since prior chemotherapy (8
weeks for mitomycin or nitrosourea) and recovered Endocrine therapy: No concurrent use of
steroids Radiotherapy: At least 4 weeks since prior radiation therapy and recovered
Surgery: Not specified