Rituximab Maintenance Versus Observation After First-line Immunochemotherapy by FCR in Older Patients With Chronic Lymphocytic Leukemia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

542 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-12-31

Study Completion Date

2017-07-31

Brief Summary

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RATIONALE: Classical chemotherapy does not cure advanced chronic lymphocytic leukemia (CLL) despite new drugs. Rituximab is a monoclonal antibody directed against CD20 surface antigen on B lymphocytes and leads to apoptosis of CD20 positive B lymphocytes. The highest response rate yet published in the treatment of first-line CLL has been obtained by the association of fludarabine, cyclophosphamide and rituximab (FCR). Now, the question is whether this response can be improved, as some trials showed that eradication of minimal residual disease (MRD) in CLL is associated with a longer treatment-free and overall survival. Maintenance therapy using rituximab has been recently approved as a means of prolonging remission in patients with indolent non Hodgkin's lymphoma. Maintenance therapy with rituximab could be of interest in treatment of MRD in CLL and prolonging remission and survival times.

PURPOSE: The overall purpose of the study is to determine the value of immunotherapy maintenance with single agent rituximab in comparison with no further treatment (observation ) for previously untreated chronic lymphocytic leukaemia in elderly (\>65 years) patients who respond to induction immunochemotherapy with FCR.

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Detailed Description

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OBJECTIVES:

Primary

* To demonstrate superiority, in terms of 3-year progression-free survival (PFS), of rituximab maintenance over observation in patients who are in complete or partial response (CR or PR) after induction therapy comprising fludarabine, cyclophosphamide, and rituximab.

Secondary

* To determine event-free survival, disease-free survival, overall survival, and time to next treatment, all from time of randomization.
* To determine overall response rate (CR and PR) according to NCI and iwCLL criteria
* To assess the rate of phenotypic response (minimal residual disease).
* To assess duration of phenotypic and NCI and iwCLL clinical responses.
* To determine response rates and time-related parameters in biological subgroups.
* To determine rates of treatment-related adverse events.
* To evaluate CD4/CD8 counts, immunoglobulin levels, and incidence of Coombs-positive hemolytic anemia.
* To study pharmacokinetics of rituximab during induction and maintenance.
* To evaluate the prognostic impact of the immunoglobulin FcγRIIIA genotype.
* To assess quality of life.
* To study pharmacoeconomics.

OUTLINE: This is a multicenter study. Randomization is stratified according to response to induction therapy (complete response \[CR\] vs partial response \[PR\]), IGHV mutational status, and 11q deletion.

Patients receive rituximab IV on days 1 and 14 of courses 1-2 and on day 1 of courses 3 and 4. Patients also receive oral fludarabine and oral cyclophosphamide once daily on days 2-4 of course 1 and on days 1-3 of courses 2-4. Courses are administered every 28 days. Patients achieving CR or PR are randomized 1:1 to maintenance arm or observation arm.

* Arm A: Patients receive rituximab IV every 2 months in the absence of disease progression or unacceptable toxicity for a maximum duration of 24 months (12 infusions).
* Arm B: Patients undergo observation only.

After completion of study therapy, patients are followed every 3 months for 1 year and then every 6 months for 2 years.

Conditions

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Leukemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Observation

Observation every 8 weeks during 2 years

Group Type NO_INTERVENTION

No interventions assigned to this group

rituximab arm

rituximab :500 mg/m² every 8 weeks during 2 years

Group Type EXPERIMENTAL

Rituximab

Intervention Type BIOLOGICAL

rituximab :500 mg/m² every 8 weeks during 2 years

Interventions

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Rituximab

rituximab :500 mg/m² every 8 weeks during 2 years

Intervention Type BIOLOGICAL

Other Intervention Names

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Mabthera

Eligibility Criteria

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Inclusion Criteria

* B-CLL
* Matutes score 4 or 5
* Binet stages B or C
* Age \> 65 years old
* No previous treatment of CLL by chemotherapy, radiotherapy or immunotherapy, except glucocorticoids \< 1 month
* Patient's written informed consent
* Life expectancy \> 6 months

* Patients having received the full induction phase with 4 FC and 6 rituximab courses (with/without dose adjustments as per protocol)
* Complete or partial response according to NCI and iwCLL criteria at the end of induction phase
* Recovery from FCR toxicities
* Patient willingness to continue on protocol

Exclusion Criteria

* Binet stage A
* ECOG performance status 2 or more
* Presence of a 17p deletion by FISH (\> 10% positive cores)
* Clinically significant auto-immune cytopenia, Coombs-positive hemolytic anemia as judged by the treating physician
* Patients with a history of another malignancy in complete remission less than 5 years, except basal cell skin cancer or tumor treated curatively by surgery
* Concomitant disease requiring prolonged use of corticosteroids (\> 1 month)
* Any severe co-morbidities such as NYHA Class III or IV heart failure, myocardial infarction within 6 months, unstable angina, ventricular tachyarrhythmias requiring ongoing treatment, severe uncontrolled myocardiopathy, uncontrolled hypertension, severe chronic obstructive pulmonary disease with hypoxemia, or uncontrolled diabetes mellitus.
* CIRS (Cumulative Illness rating Scale) \> 6
* Known hypersensitivity to murine proteins or to any of the study drugs or to their components
* Transformation into an aggressive B-cell malignancy (e.g. diffuse large cell lymphoma, Hodgkin lymphoma) or prolymphocytic leukemia
* Active bacterial, viral or fungal infection
* Seropositivity HIV, hepatitis C or hepatitis B (unless clearly due to vaccination)
* Total bilirubin, alkaline phosphatases and aminotransferases \> 2 x ULN
* Creatinine clearance \< 60 ml/min calculated according to the formula of Cockcroft and Gault
* Any coexisting medical or psychological condition that would preclude participation to the required study procedures
* Patient with mental deficiency preventing proper understanding of the requirements of treatment

Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No