Allogeneic Stem Cell Transplantation in Chronic Lymphocytic Leukemia

Phase 2

• Conditions: Chronic Lymphocytic Leukemia
• Interventions: Procedure: allogeneic stem cell transplantation; Drug: Alemtuzumab

• Registration Number: NCT00337519
• Lead Sponsor: Charite University, Berlin, Germany

Brief Summary

Patients with advanced chronic lymphocytic leukemia (CLL) have a poor long-term prognosis. Allogeneic stem cell transplantation (SCT) in patients with CLL has only rarely been performed in the past because the clinical outcome after myeloablative conditioning was poor, mainly due to the high treatment-related mortality. However long-term disease-free survival after allogeneic SCT has been reported. Recently it has been demonstrated by our group and others that non-relapse mortality can be reduced significantly with the use of reduced-intensity conditioning regimens. Yet, graft versus host disease (GVHD) remains an important problem in this setting.

Alemtuzumab is an effective drug for the treatment of patients with advanced CLL and has been successfully applied for GVHD-prophylaxis in the setting of myeloablative and reduced-intensity conditioning regimens. The goal of the present study is to evaluate the role of alemtuzumab as part of a fludarabine-based reduced intensity conditioning regimen for allogeneic SCT in patients with advanced CLL.

Detailed Description

Patients with relapsed or refractory CLL who are eligible for the study receive a cytoreductive therapy until SCT. Irrespective to the formal response, patients proceed to allogeneic SCT after fludarabine-based reduced-intensity conditioning. The use of granulocyte colony-stimulating factor (G-CSF)-mobilized peripheral blood stem cells \> 3 x 10E6 CD34 cells/kg is recommended, but bone marrow \> 1 x 10E8 MNC/kg is accepted. GVHD-prophylaxis is based on cyclosporine A adapted to blood levels (150 to 200 ng/mL) over a period of three months. In Phase I of the study, alemtuzumab has been applied as part of the conditioning regimen until day 5. In Phase II, alemtuzumab is given as cytoreductive pre-treatment with the last application of alemtuzumab scheduled for day 14 and after Amendment II in September 2006 scheduled for day 28. Furthermore methotrexate is given on days 1, 3, 6. and 11 at a projected cumulative dose of 45 mg/m2. Subsequent immunosuppressive therapy depends on the occurrence of GvHD, the development of chimerism, and residual disease. Patients with relapsing or residual disease (minimal residual disease excluded) who do not suffer from GvHD should receive donor lymphocytes in increasing dosages. The initial dose is 1 x 105/kg T-cells in unrelated donors and 1 x 106/kg in matched related donors. If no GvHD develops within 6-8 weeks, the next higher dosage is applied.

Study Timeline

• Study Start: 2003-01
• Study First Submitted: 2006-06-15
• Study First Submitted QC: 2006-06-15
• Study First Posted: 2006-06-16
• Status Verified: 2009-01
• Last Update Submitted: 2009-01-28
• Last Update Posted: 2009-01-29
• Primary Completion: 2009-04
• Study Completion: 2009-04

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 82

Inclusion Criteria

• written informed consent
• sufficient organ function
• availability of an HLA-compatible donor (related or unrelated)
• age < 65 years
• karnofsky index > = 70%
• B-CLL requiring treatment after failure of at least one prior cytostatic treatment

Read More

Exclusion Criteria

• positive HIV-serology
• pregnancy
• intolerance to study drugs
• second neoplasia
• serious infections

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
1	allogeneic stem cell transplantation	see detailed description
1	Alemtuzumab	see detailed description

Primary Outcome Measures

Name	Time	Method
Progression-free survival	400 days

Secondary Outcome Measures

Name	Time	Method
safety according to common toxicity criteria (CTC)	at discharge and until last follow up
rate of primary and secondary graft failure	until last follow up
rate of acute and chronic GVHD	day 100 and last follow up
response rate	2 years
chimerism	day 100

Trial Locations

Locations (3)

Uniklinikum Carl Gustav Carus; 🇩🇪 Dresden, Germany

Klinikum Chemnitz gGmbH; 🇩🇪 Chemnitz, Germany

Deutsche Klinik für Diagnostik GmbH; 🇩🇪 Wiesbaden, Germany