Low Dose Alemtuzumab for Consolidation and Maintenance of Patients With B-Cell Chronic Lymphocytic Leukemia
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|ClinicalTrials.gov Identifier: NCT00336206|
Recruitment Status : Unknown
Verified June 2006 by Tawam Hospital.
Recruitment status was: Not yet recruiting
First Posted : June 13, 2006
Last Update Posted : July 25, 2006
|Condition or disease||Intervention/treatment||Phase|
|B-Cell Chronic Lymphocytic Leukemia||Drug: Alemtuzumab||Not Applicable|
Fludarabine (F) alone or in combination with cyclophosphamide (FC) is not a curative treatment for patients with CLL, all patients will eventually relapse. Therefore there is a medical need to look for consolidation followed by maintenance therapies which are able to prolong response duration or which can shift anti-tumor therapy induced partial remissions to complete remissions or eradicate minimal residual disease in complete - but still PCR-positive – responders.
There is no standard consolidation therapy available at the moment and the role of consolidation in CLL has recently been acknowledged as a research field of major importance in B-CLL (Schering global advisory board meeting, Lisbon Nov 2005). Possible treatment options are high-dose chemotherapy followed by autologous stem cell transplantation (the role of which however remains uncertain with lack of worldwide consensus) or monoclonal antibody therapy against antigens expressed by CLL cells. Alemtuzumab is directed against the CD52-antigen which is present in high density on CLL cells and may therefore be most suitable for treatment of residual disease.
Alemtuzumab has shown significant remission rates in patients with fludarabine refractory CLL and sub analysis revealed a very high effectiveness of the antibody in clearing CLL cells from peripheral blood and bone marrow. These findings suggest that Alemtuzumab might be an ideal candidate to eliminate minimal residual disease in a post-remission treatment after anti-tumor therapy and to be used as maintenance therapy. The efficacy of Alemtuzumab as consolidation therapy in CLL can easily be measured. There is evidence from several studies that treatment with Alemtuzumab does not have a negative impact on stem cell mobilization. Therefore, autologous stem cell transplantation still remains as a further treatment option for those patients who still have detectable disease after primary cytoreduction followed by consolidation therapy with Alemtuzumab.
Side effects of s.c. Alemtuzumab in heavily pretreated patients with advanced disease are tolerable and manageable. Data have suggested that the safety profile of this antibody is even more favorable in less pretreated patients and the GCLLSG study suggests that a wash-out period of more than 8 weeks and possibly also a lower dose is necessary to avoid severe infectious problems. Campath administration started after a 2-month wash out period after Fludarabine was shown to be feasible and good tolerated. Based on the collective data obtained from other pilot or phase II studies, a subcutaneous consolidation dose of 30 mg once weekly in previously treated and untreated CLL patients after an induction with Fludarabine combination seems to be a safe and effective dose.
The proposed study aims to evaluate the efficacy of low dose treatment with Alemtuzumab with regard to the following questions: Does consolidation therapy with low dose Alemtuzumab result in a prolonged time to disease progression in comparison to patients who do not receive further treatment? Is it possible to turn a PR into a CR? Does maintenance therapy with Alemtuzumab translate into a progression-free survival benefit compared to patients with no further treatment? How is the safety profile in patients treated with low dose Alemtuzumab as MRD elimination and as maintenance therapy?
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||60 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Subcutaneous Injection, Low Dose Alemtuzumab for Consolidation and Maintenance of Patients in Clinical Response After Having Achieved Partial or Complete Remission After 1st or 2nd Line Anti-Tumor Therapy for B-Cell CLL|
|Study Start Date :||July 2006|
|Study Completion Date :||October 2009|
- To determine the Time to Treatment Failure (TTF)
- To evaluate Complete Remission (CR) rate.
- To evaluate Partial Response (PR) rate.
- Minimal Residual Disease (MRD) evaluated with flow-cytometry (“MRD flow panel”) in patients with CR
- To determine Overall Response Rate (ORR).
- To evaluate duration of response.
- To evaluate safety
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00336206
|Contact: Jorgen Kristensen, MD PhD||971 3 7677444 ext email@example.com|
|Principal Investigator:||Jorgen Kristensen, MD PhD||Department of Oncology|