Dose Escalation Study of Gleevec and Chlorambucil in Previously Treated Chronic Lymphocytic Leukemia Patients (GL-CLB-001)

Jewish General Hospital

Status and phase

Terminated

Phase 2

Phase 1

Conditions

Chronic Lymphocytic Leukemia

Treatments

Drug: Gleevec and Chlorambucil

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00558961

CR0506PI

REC:05-054

Details and patient eligibility

About

The purpose of this study is to determine maximum tolerated dose of Gleevec in combination with Chlorambucil in previously treated CLL patients.

Full description

A recent study by Aloyz et al demonstrated a synergistic effect of imatinib on chlorambucil-mediated cytotoxicity in CLL cells in vitro. Imatinib inhibits c-abl and sensitizes cells to chlorambucil. The Phase I component of the study will determine the maximum tolerated dose and recommended Phase II dose of Gleevec when used in combination with chlorambucil. Once the maximum tolerated dose has been determined, a total of 16 patients will be enrolled in the Phase II component of the study. This study will determine the dose limiting toxicities, pharmacokinetics and pharmacodynamics of Gleevec in combination with chlorambucil.

Enrollment

13 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

B-cell chronic lymphocytic leukemia (a) Rai stage 0-II with indication for treatment by NCI Working Group Criteria: or (b) Rai stage III or IV.
Received a minimum of one prior chemotherapy regimen. Prior treatment with corticosteroids, immunotherapies, monoclonal antibodies or radiation therapy is permitted.
White blood cell count > 25 x 10^9/L
ECOG 0, 1,or 2.
Adequate renal and hepatic function
Platelets > 75 x 10^9/L, transfusion independent.
Neutrophils > 1.0 x 10^9/L, transfusion independent

Exclusion criteria

Documented prolymphocytic leukemia (PLL; prolymphocytes, 55% in blood)
Active cardiovascular disease as defined by NYHA class III-IV categorization.
Intercurrent illness or medical condition precluding safe administration of ribavirin.
Concurrent use of chronic steroids, except as replacement therapy for adrenal insufficiency
Known infection with HIV, Hepatitis B or C.
Concurrent malignancy (other than resected basal or squamous cell skin cancers or in-situ carcinoma).
Received any previous therapy for CLL within 28 days prior to study entry.