Fludarabine/Rituximab Combined With Escalating Doses of Lenalidomide in Untreated CLL

Sponsor

Arbeitsgemeinschaft medikamentoese Tumortherapie (Other)

Overall Status

Completed

CT.gov ID

NCT01703364

Collaborator

Celgene (Industry)

Enrollment

Locations

Arm

Duration (Months)

Patients Per Site

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a trial in patients with previously untreated CLL. Eligible patients will receive Lenalidomide with a backbone of Fludarabine and Rituximab for 6 therapy cycles. Lenalidomide will be increased by dose steps of 5 mg every cycle in the absence of limiting toxicity. If limiting toxicity ensues the patients will be treated with last tolerable dose for the remainder of the 6 treatment cycles.

The first 5 patients will start with dose level 5 mg Lenalidomide and further escalating dose. After the fifth patient is included in the study, enrolment will be interrupted until this patient has finished his first treatment cycle. A safety board will evaluate the toxicities of the first 5 patients. If there are more than 2 patients experiencing a dose limiting toxicity (DLT) in the first treatment cycle, the starting dose will not be escalated and further 5 patients will be enrolled with a starting dose of 5 mg Lenalidomide. If only 2 or less patients experience a DLT in the first treatment cycle, the next 5 patients will start the treatment with 10 mg Lenalidomide.

The rational for the higher starting doses stems from the lack of tumor lysis or tumor flare toxicity in this combination on the one hand and from the observation that the very slow escalation from 2,5 mg on led to a lack of efficacy in monotherapy trials due to early progression in a relevant number of cases. The increase of the Lenalidomide dosage should result in an increased efficacy especially at the beginning and a higher cumulative dose of Lenalidomide.

The identification of patients intolerant to Lenalidomide by immunophenotyping of the T cells for validation is also part of this trial, because intolerance seems to be not dose dependent but may be caused by T cell activation. Therefore, early identification of patients intolerant to this form of modern immunochemotherapy and establishing efficient Lenalidomide based combination therapy is an important part of improvement of current CLL treatment.

Condition or Disease	Intervention/Treatment	Phase
CLL Chronic Lymphocytic Leukemia	Drug: Lenalidomide	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

12 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Fludarabine/Rituximab Combined With Escalating Doses of Lenalidomide in Untreated Chronic Lymphocytic Leukemia (CLL) - a Dose-finding Study With Escalating Starting Dose of Lenalidomide and Concomitant Evaluation of Safety and Efficacy

Study Start Date :

Jun 1, 2012

Actual Primary Completion Date :

Mar 1, 2015

Actual Study Completion Date :

Oct 1, 2015

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Lenalidomide/Fludarabine/Rituximab Lenalidomide: day 8-21 of cycle 1 and day 1-21 of cycles 2-6; Starting Dose: 5 mg (first 5 patients) and 10 mg (further 5 patients) increase Lenalidomide dose via dose levels (10)/15/20/25 mg/d every 28 days if no limiting toxicity occurs Fludarabine: 25 mg/m2 iv d1-3 or 40 mg/m2 po d1-3; repeat every 28 days Rituximab: 375 mg/m2 iv day 4 on cycle 1 and 500 mg/m2 iv day 1 on cycles 2-6; repeat every 28 days	Drug: Lenalidomide Lenalidomide: day 8-21 of cycle 1 and day 1-21 of cycles 2-6; Starting Dose: 5 mg (first 5 patients) and 10 mg (further 5 patients) increase Lenalidomide dose via dose levels (10)/15/20/25 mg/d every 28 days if no limiting toxicity occurs Fludarabine: 25 mg/m2 iv d1-3 or 40 mg/m2 po d1-3; repeat every 28 days Rituximab: 375 mg/m2 iv day 4 on cycle 1 and 500 mg/m2 iv day 1 on cycles 2-6; repeat every 28 days Other Names: Revlimid

Arm

Intervention/Treatment

Experimental: Lenalidomide/Fludarabine/Rituximab

Lenalidomide: day 8-21 of cycle 1 and day 1-21 of cycles 2-6; Starting Dose: 5 mg (first 5 patients) and 10 mg (further 5 patients) increase Lenalidomide dose via dose levels (10)/15/20/25 mg/d every 28 days if no limiting toxicity occurs Fludarabine: 25 mg/m2 iv d1-3 or 40 mg/m2 po d1-3; repeat every 28 days Rituximab: 375 mg/m2 iv day 4 on cycle 1 and 500 mg/m2 iv day 1 on cycles 2-6; repeat every 28 days

Drug: Lenalidomide

Other Names:

Revlimid

Outcome Measures

Primary Outcome Measures

Tolerability of escalated starting dose [12 month, 20 month]
Interim analysis after completion of cylce 1 of the first 5 patients, final analysis after last pastient last visit Metrics: Number of patients experiencing defined dose limiting toxicities during cycle 1

Secondary Outcome Measures

Establishment of maximal tolerated dose (MTD) of Lenalidomide in combination with FR [20 month]
Time to MTD [20 month]
Safety profile of the FRL combination [20 month]
Analysis of occuring adverse events during the study treatment according to Common Terminology Criteria for Adverse Events (CTCAE)
Response rates in all phases by 4-colour flow cytometric and ASO-PCR MRD analysis [20 month]
Risk factor analysis (FISH cytogenetics, CD38/ZAP-70 expression, mutation status) [20 month]
Longitudinal definition of T cell subsets (including prognostic EM T cells and Treg cells)+/- PD1 [20 month]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Signed written informed consent
Male or female ≥ 18 years of age
CLL (as determined by CD23+, CD5+, CD19+)
Treatment indication as defined by the NCI Workshop criteria (see appendix 6 and reference 10)
ECOG ≤ 2
No previous treatment of the CLL by chemotherapy, radiotherapy (except localized radiotherapy of 1 lymphatic area) or immunotherapy
Life expectancy > 6 months (except prognosis due to high risk CLL)

Exclusion Criteria:

Active bacterial, viral or fungal infection
Positivity for HIV, Hepatitis B or C
Patients with known history of thromboembolic events
Reduced organ functions and bone marrow dysfunction not due to CLL
Creatinine clearance of below 30 ml/min
Patients with known history of thromboembolic events
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)
Patients with medical co-morbid conditions that would require long term use (> 1 month) of systemic corticosteroids during study treatment
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
Other known co-morbidity with the potential to dominate survival
Transformation to aggressive B-cell malignancy (e.g., large B-cell lymphoma, Richter's syndrome, or prolymphocytic leukemia (PLL))
Hypersensitivity with anaphylactic reaction to humanised monoclonal antibodies or any of the applied drugs
Concurrent chronic systemic immune therapy, chemotherapy, or hormone therapy not indicated in the study protocol
Administration of any investigational agent(s) within 4 weeks prior to entry
Pregnancy or lactation
Medical or psychological condition which in the opinion of the Investigator would not permit the patient to complete the study or sign meaningful informed consent

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Universitätsklinik für Innere Medizin Innsbruck, Klinische Abteilung für Hämatologie und Onkologie	Innsbruck	Tirol	Austria	6020
2	Universitätsklinik der PMU Salzburg, Univ-Klinik für Innere Medizin III	Salzburg		Austria	5020