Bendamustine Combined With Alemtuzumab in Pretreated Chronic Lymphocytic Leukemia (CLL)

Sponsor

Arbeitsgemeinschaft medikamentoese Tumortherapie (Other)

Overall Status

Completed

CT.gov ID

NCT00951457

Collaborator

Mundipharma Pte Ltd. (Industry)

Enrollment

Locations

Arm

41.2

Duration (Months)

2.9

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The primary objective of this study is to determine the percentage of patients achieving a response, defined as the percentage of patients achieving complete response, partial response and stable disease/ no change upon treatment with the combination therapy according to NCI response criteria (also established according to IWCLL guidelines) upon treatment with a combination of bendamustine and alemtuzumab.

Condition or Disease	Intervention/Treatment	Phase
Leukemia, Lymphocytic, Chronic, B-Cell	Drug: Bendamustine Drug: Alemtuzumab	Phase 1/Phase 2

Detailed Description

This is a non-randomized, multicenter, open-label, single-arm Phase I/II study to evaluate the safety and efficacy of bendamustine combined with alemtuzumab in patients with pretreated CD20-positive CLL (according to the revised NCI/ IWCLL criteria).

Eligible patients will receive bendamustine as 4 courses of 70 mg/m2 on days 1 and 2 every 28 days and 30 mg alemtuzumab s.c. continuously on days 1, 3 and 5 of every week, for a maximum of 16 weeks. Safety assessments will be conducted weekly; efficacy assessments including imaging will be performed at months 2, 4, 6, 10 and 16. Bone marrow biopsies will be performed upon CR (according to the 2008 IWCLL response criteria) or fixed at 6 and 16 months.

Following recruitment of the first 3 and 7 patients safety evaluations will be performed by a data safety monitoring board. An interim analysis for response and safety as well as maximum tolerated dose levels will occur after the first 7 patients have completed treatment (Gehan timepoint). If the treatment is deemed clinically safe a further 13 patients will be enrolled.

Study Design

Study Type:

Interventional

Actual Enrollment :

20 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Bendamustine Combined With Alemtuzumab in Pretreated Chronic Lymphocytic Leukemia (CLL) - A Phase I/II Trial With Concomitant Evaluation of Safety and Efficacy

Study Start Date :

Mar 1, 2009

Actual Primary Completion Date :

Aug 6, 2012

Actual Study Completion Date :

Aug 6, 2012

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Overall study Dose escalation phase: Days -3, -2, -1: 3 - 10 - 30 mg Alemtuzumab s.c. Treatment phase: Bendamustine 70 mg/m2 i.v. on d1 + d2 repeat every 28 days for 4 cycles Alemtuzumab 30 mg s.c. 3x per week (days 1, 3, 5) continuously in parallel with chemotherapy cycles for a maximum of 16 weeks	Drug: Bendamustine Other Names: Ribomustin Drug: Alemtuzumab

Arm

Intervention/Treatment

Experimental: Overall study

Dose escalation phase: Days -3, -2, -1: 3 - 10 - 30 mg Alemtuzumab s.c. Treatment phase: Bendamustine 70 mg/m2 i.v. on d1 + d2 repeat every 28 days for 4 cycles Alemtuzumab 30 mg s.c. 3x per week (days 1, 3, 5) continuously in parallel with chemotherapy cycles for a maximum of 16 weeks

Drug: Bendamustine

Other Names:

Ribomustin

Drug: Alemtuzumab

Outcome Measures

Primary Outcome Measures

To determine the percentage of patients achieving a response, defined as the percentage of patients achieving complete response, partial response and stable disease/ no change upon treatment with the combination therapy [2 -16 months]

Secondary Outcome Measures

To evaluate the efficacy of a bendamustine/ alemtuzumab combination therapy in terms of complete response rates [2 - 16 months]
To evaluate the achievable cumulative doses of bendamustine and alemtuzumab in terms of maximum tolerated doses while on treatment [2 -16 months]
To determine response rates in all phases by 4-colour flow cytometric MRD analysis [2 -16 months]
To identify and characterize potential risk factors via FISH cytogenetics, CD38/ Zap-70 expression and mutational status [2 - 6 months]
To define clonal evolution by use of longitudinal FISH cytogenetics [2 - 6 months]
To define T cell subsets including prognostic EM T cells and Treg cells [2 - 16 months]
To document change upon quality of life by use of a standardized QoL questionnaire [2 -16 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female patients with CD23+, CD5+, CD19+ light chain monoclonal B-CLL with treatment indication according to IWCLL criteria (Appendix 4)
1st or greater relapse after fludarabine or any other primary treatment regimen OR Refractory to any previous treatment and simultaneous indication for treatment according to IWCLL criteria (Appendix 4)
Age 18 years and older
ECOG status 0 - 2
Life expectancy > 6 months
Written informed consent given by the patient
Patient using a reliable means of contraception (e.g. physical barrier, contraceptive pill or patch, spermicide and barrier, or IUD) for the duration of the study. Male patients have to use an adequate contraception method for the duration of study treatment and for 6 months following completion of study treatment. Women of childbearing potential have to use an effective method of contraception for the duration of study participation.

Exclusion Criteria:

HIV positive or positive for Hepatitis B or C
Active uncontrolled infection
Pregnant or lactating women
Hypersensitivity with anaphylactic reaction to humanised monoclonal antibodies or to the excipients of any of the applied drugs (e.g. Bendamustine hydrochloride or mannitol)
Previous treatment with bendamustine
Treatment with an experimental drug within the previous 2 months
Patients with a history of other malignancies within 2 years prior to study entry, except for adequately treated carcinoma in situ of the cervix; basal or squamous cell skin cancer; low grade, early stage localized prostate cancer treated surgically with curative intent; good prognosis DCIS of the breast treated with lumpectomy alone with curative intent.
Transformation to aggressive B-cell malignancy (e.g. large B-cell lymphoma, Richter's syndrome, or prolymphocytic leukemia (PLL)
Decreased kidney function with creatinine clearance < 30 ml/min
Patients with severe co-morbidities or major organ dysfunctions (e.g. known severe liver damage, jaundice)
Patients with a history of severe cardiac disease; e.g. NYHA Functional Class III or IV heart failure, myocardial infarction within 6 months, ventricular tachyarrhythmias requiring ongoing treatment, or unstable angina
Any co-existing medical or psychological condition that would preclude participation in the study or compromise ability to give informed consent, or patients unable to comply with requirements of study protocol

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Medizinische Universitaet Innsbruck, Abtlg. f. Haematologie und Onkologie	Innsbruck	Tirol	Austria	A-6020
2	Landeskrankenhaus Feldkirch	Feldkirch		Austria	A-6806
3	A.ö. Landeskrankenhaus Leoben	Leoben		Austria	A-8700
4	Krankenhaus der Elisabethinen Linz	Linz		Austria	A-4010
5	Krankenhaus der Stadt Linz	Linz		Austria	A-4020
6	Universitaetsklinik f. Innere Medizin III	Salzburg		Austria	A-5020
7	Klinikum Wels-Grieskirchen GmbH	Wels		Austria	A-4600