Clinical Trials Directory

Trials / Terminated

TerminatedNCT00009984

Thalidomide With or Without Fludarabine in Treating Patients With Hematologic Cancer

Randomized Phase II Study of Thalidomide Versus Thalidomide Plus Fludarabine for Patients With Chronic Lymphocytic Leukemia Previously Treated With Fludarabine

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
70 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This randomized phase II trial is studying thalidomide and fludarabine to see how well they work compared to thalidomide alone in treating patients with hematologic cancer that has not responded to previous treatment with fludarabine. Thalidomide may stop the growth of hematologic cancer by stopping blood flow to the cancer. Combining thalidomide with fludarabine may increase the effectiveness of chemotherapy by making cancer cells more sensitive to the drug. It is not yet known whether thalidomide is more effective with or without fludarabine for hematologic cancer.

Detailed description

OBJECTIVES: I. Compare the safety and tolerability of thalidomide with or without fludarabine in patients with fludarabine-refractory chronic lymphocytic leukemia or small lymphocytic lymphoma. II. Compare the incidence of complete and partial remission in patients treated with these regimens. OUTLINE: This is a randomized, open-label study. Patients are stratified according to time to relapse from last fludarabine treatment (less than 6 months vs more than 6 months). Patients are randomized to one of two treatment arms. Arm I: Patients receive oral thalidomide once daily in the absence of disease progression or unacceptable toxicity. Arm II: Patients receive thalidomide as in arm I and fludarabine IV over 30 minutes on days 1-5. Treatment with fludarabine repeats every 28 days for 6 courses. Once fludarabine is completed, patients continue to receive thalidomide alone as in arm I. PROJECTED ACCRUAL: A total of 24-70 patients (12-35 per treatment arm) will be accrued for this study within 1 year.

Conditions

Interventions

TypeNameDescription
DRUGfludarabine phosphateGiven IV
DRUGthalidomideGiven orally

Timeline

Start date
2002-03-01
Primary completion
2006-11-01
First posted
2003-01-27
Last updated
2013-06-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00009984. Inclusion in this directory is not an endorsement.