Thalidomide With or Without Fludarabine in Treating Patients With Hematologic Cancer

NCT ID: NCT00009984

Last Updated: 2013-06-06

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-03-31

Brief 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

Recurrent Small Lymphocytic Lymphoma; Refractory Chronic Lymphocytic Leukemia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I (thalidomide)

Patients receive oral thalidomide once daily in the absence of disease progression or unacceptable toxicity.

Group Type: EXPERIMENTAL

thalidomide

Intervention Type: DRUG

Given orally

Arm II (thalidomide, fludarabine phosphate)

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.

Group Type: EXPERIMENTAL

fludarabine phosphate

Intervention Type: DRUG

Given IV

thalidomide

Intervention Type: DRUG

Given orally

Interventions

fludarabine phosphate

Given IV

Intervention Type: DRUG

thalidomide

Given orally

Intervention Type: DRUG

Other Intervention Names

2-F-ara-AMP; Beneflur; Fludara; Kevadon; Synovir; THAL; Thalomid

Eligibility Criteria

Inclusion Criteria

• Diagnosis of one of the following:

• Confirmed chronic lymphocytic leukemia (CLL), meeting the following criteria:

• Peripheral blood lymphocytosis greater than 5,000/mm^3
• Co-expression of the CD5, CD19, CD20, and CD23 surface antigens
• Clonal kappa and lambda light chain expression
• Dim surface immunoglobulin expression
• Small lymphocytic lymphoma
• Relapsed or refractory disease

• Must have received at least 1 prior regimen containing fludarabine
• Meets one of the following criteria:

• Recurrence of lymphocytosis greater than 5,000/mm^3 or an increase in lymph node volume greater than 50% after achieving complete (CR) or partial response (PR)
• Never achieved a CR or PR after receiving at least 2 courses of fludarabine IV for 5 days at a dose of 25 mg/m^2/day
• No other lymphoproliferative diseases or diseases due to transformation of CLL (e.g., prolymphocytic leukemia or Richter's syndrome)
• No known CNS disease
• Performance status - Karnofsky 60-100%
• At least 12 weeks
• See Disease Characteristics
• Bilirubin < 2.0 times upper limit of normal (ULN)*
• SGOT < 2.5 times ULN*
• Creatinine < 1.5 times ULN
• No history of cardiac arrhythmia
• No myocardial infarction within the past 6 months
• No other malignancy within the past 5 years except basal cell skin cancer or carcinoma in situ of the cervix
• No active serious infection uncontrolled by antibiotics
• No pre-existing neurotoxicity grade 3 or greater
• No other medical condition that would preclude study participation
• Not pregnant or nursing
• Negative pregnancy test
• Female patients must use 2 effective methods (at least 1 highly active method) of contraception 4 weeks before, during, and for 4 weeks after study participation and male patients must use effective barrier contraception during and for 4 weeks after study participation
• At least 4 weeks since prior biologic therapy and recovered
• No concurrent growth factors (epoetin alfa, filgrastim [G-CSF], or sargramostim [GM-CSF])
• See Disease Characteristics
• No more than 3 prior chemotherapy regimens
• At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas) and recovered
• No other concurrent chemotherapy
• At least 4 weeks since prior radiotherapy and recovered
• No concurrent radiotherapy
• Recovered from any prior investigational agents
• No other concurrent investigational agents

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Richard Furman

Role: PRINCIPAL_INVESTIGATOR

Montefiore Medical Center

Locations

Montefiore Medical Center

The Bronx, New York, United States

Countries

United States

Other Identifiers

NYWCCC-MTS-00-0535ME

Identifier Type: -

Identifier Source: secondary_id

CDR0000068429

Identifier Type: -

Identifier Source: secondary_id

NCI-639

Identifier Type: -

Identifier Source: secondary_id

N01CM62204

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2012-02393

Identifier Type: -

Identifier Source: org_study_id