RATIONALE: Giving chemotherapy before a peripheral stem cell transplant stops the growth of cancer cells by stopping them from dividing or killing them. Giving colony-stimulating factors, such as G-CSF, and certain chemotherapy drugs, helps stem cells move from the bone marrow to the blood so they can be collected and stored. Chemotherapy or radiation therapy is then given to prepare the bone marrow for the stem cell transplant. The stem cells are then returned to the patient to replace the blood-forming cells that were destroyed by the chemotherapy and radiation therapy. PURPOSE: This phase II trial is studying how well giving cyclophosphamide together with total-body irradiation works in treating patients who are undergoing an peripheral stem cell transplant for chronic lymphocytic leukemia.
OBJECTIVES: Primary * Determine the safety and feasibility of autologous peripheral blood stem cell transplantation in patients with chronic lymphocytic leukemia treated with cyclophosphamide and total-body irradiation. Secondary * Determine the safety, feasibility, and efficacy of combination therapy comprising dexamethasone, carmustine, cytarabine, etoposide, and melphalan (Dexa-BEAM) and filgrastim (G-CSF) mobilization in patients treated with this regimen. * Determine the efficacy of ex-vivo graft purging in patients treated with this regimen. * Determine the incidence of complete clinical and molecular remissions in patients treated with this regimen. * Determine the progression-free survival of patients treated with this regimen. OUTLINE: This is a multicenter, open-label, nonrandomized study. * Cytoreductive treatment: Patients undergo 2-4 courses of cytoreductive treatment, preferably following the fludarabine and cyclophosphamide (FC) protocol. * Stem cell mobilization: Patients achieving a complete remission (CR) or partial remission (PR) and stable blood counts undergo stem cell mobilization comprising dexamethasone, carmustine, cytarabine, etoposide, melphalan (Dexa-BEAM), and filgrastim (G-CSF). Patients with an adequate number of mobilized cells undergo stem cell collection. Patients with CR or very good PR proceed to myeloablative therapy. * Myeloablative therapy: Patients undergo total-body irradiation on day -4 and receive cyclophosphamide IV on days -4 and -3. * Autologous peripheral blood stem cell transplantation (PBSCT): Patients undergo autologous PBSCT on day 0. After completion of study, patients are followed periodically. PROJECTED ACCRUAL: A total of 150 patients will be accrued for this study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
169
Allg. Krankenhaus der Stadt Wien Universitaets-Kinderklinik
Vienna, Austria
Hanuschkrankenhaus
Vienna, Austria
Humaine - Clinic
Bad Saarow, Germany
Charite - Universitaetsmedizin Berlin - Campus Benjamin Franklin
Berlin, Germany
Robert Roessle Comprehensive Cancer Center at University of Berlin - Charite Campus Buch
Berlin, Germany
Safety of autologous peripheral stem cell transplantation (PBSCT) as measured by a treatment-related mortality of < 5% at 12 months following transplant
Feasibility of PBSCT as measured by > 50% of included patients proceeding to transplant
Safety of mobilization comprising dexamethasone, carmustine, cytarabine, etoposide, and melphalan (Dexa-BEAM) as measured by a treatment-related mortality of < 5% before transplant phase
Efficacy of Dexa-BEAM mobilization as measured by the amount of CD34+ cells > 4x10e6/kg at harvest
Complete clinical remissions by NIH criteria at 3 months following transplant
Molecular remissions by CDR3 PCR at 3 months following transplant
Progression-free survival by NIH criteria at 5 years from study entry
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Universitaetsklinikum Bonn
Bonn, Germany
Praxis Dres. F.& G. Doering
Bremen, Germany
Universitatsklinikum Carl Gustav Carus
Dresden, Germany
Michael Schaefers und Partner
Duisburg, Germany
Universitaetsklinikum Duesseldorf
Düsseldorf, Germany
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