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Cladribine and Rituximab as Remission Induction Therapy Followed By Rituximab and Stem Cell Mobilization in Treating Patients With CLL

Phase 2
Completed
Conditions
Leukemia
Registration Number
NCT00072007
Lead Sponsor
Swiss Group for Clinical Cancer Research
Brief Summary

RATIONALE: Drugs used in chemotherapy, such as cladribine, use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies, such as rituximab, can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Combining cladribine with rituximab may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving cladribine and rituximab as remission induction therapy together with rituximab and stem cell mobilization in treating patients with chronic lymphocytic leukemia.

Detailed Description

OBJECTIVES:

Primary

* Determine the efficacy and tolerability of cladribine and rituximab as remission induction therapy in patients with chronic lymphocytic leukemia.

* Determine the complete remission rate in patients treated with this regimen.

Secondary

* Determine the very good partial remission rate and nodular partial remission rate in patients treated with this regimen.

* Determine the toxicity of this regimen, in terms of hemotoxicity and infection rate, in these patients.

* Determine the efficacy of in vivo purging with rituximab measured by immunophenotyping in these patients.

* Determine the feasibility of stem cell harvest in these patients after treatment with this induction therapy regimen and in vivo purging with rituximab.

OUTLINE: This is a multicenter study.

* Remission induction: Patients receive cladribine subcutaneously (SC) on days 1-5. During courses 2-4, patients also receive rituximab IV on day 1. Treatment repeats every 28 days for up to 4 courses in the absence of unacceptable toxicity. If unacceptable toxicity persists, patients receive rituximab alone.

Patients not achieving a complete remission (CR), very good partial remission (VGPR), or nodular partial remission (NPR) receive CHOP chemotherapy comprising cyclophosphamide IV, doxorubicin IV, and vincristine IV on day 1 and oral prednisone on days 1-5. Treatment repeats every 21 days for up to 4 courses or until patients achieve a CR, VGPR, or NPR.

Patients achieving a CR, VGPR, or NPR proceed to stem cell mobilization and in vivo purging.

* Stem cell mobilization and in vivo purging: Beginning 8-10 weeks after the first day of the last course of remission induction or CHOP, patients receive rituximab IV on days 1 and 8, cyclophosphamide IV over 4 hours on day 2, and filgrastim (G-CSF) SC daily beginning on day 4 and continuing until the last day of apheresis. Patients undergo apheresis on days 11-14.

PROJECTED ACCRUAL: A total of 17-41 patients will be accrued for this study within 3 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
43
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Complete-remission rate after induction30 days
Secondary Outcome Measures
NameTimeMethod
Very good partial remission and nodular partial remission after induction30 days
Toxicity (hematotoxicity and infection rate) at 30 days following study treatment30 days

Trial Locations

Locations (11)

Hopital des Cadolles, Neuchatel

🇨🇭

Neuchatel, Switzerland

Spitaeler Chur AG

🇨🇭

Chur, Switzerland

Kantonsspital - St. Gallen

🇨🇭

St. Gallen, Switzerland

Oncology Institute of Southern Switzerland

🇨🇭

Bellinzona, Switzerland

Centre Hospitalier Universitaire Vaudois

🇨🇭

Lausanne, Switzerland

Inselspital Bern

🇨🇭

Bern, Switzerland

Kantonspital Aarau

🇨🇭

Aarau, Switzerland

Praxis Dr. Beretta

🇨🇭

Rheinfelden, Switzerland

Kantonsspital, Luzerne

🇨🇭

Luzerne, Switzerland

Onkozentrum

🇨🇭

Zurich, Switzerland

UniversitaetsSpital Zuerich

🇨🇭

Zurich, Switzerland

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