Lenalidomide and Rituximab in Treating Patients With Non-Hodgkin Lymphoma

Lymphoma Clinical Trial

Official title:

A Phase II Trial of the Combination of Lenalidomide and Rituximab in Patients With Relapsed/Refractory Follicular NHL (RV 0163)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00848328
• Other study ID #: 220942
• Secondary ID: CDR0000634775CEL
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: August 25, 2008
• Est. completion date: December 2024

Study information

• Verified date: August 2023
• Source: University of California, Davis
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving lenalidomide together with rituximab may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving lenalidomide together with rituximab works in treating patients with follicular or small lymphocytic non-Hodgkin lymphoma that has relapsed or not responded to treatment.

Description:

OBJECTIVES:

Primary

• To determine the response rate in patients with relapsed or refractory follicular or small lymphocytic non-Hodgkin lymphoma treated with lenalidomide and rituximab.

Secondary

• To determine the time to disease progression, duration of response, and overall survival of these patients.

• To determine the tolerability of this regimen in these patients.

• To assess changes in serum cytokines before and after treatment and correlate these changes with response.

OUTLINE: This is a multicenter study.

Patients receive oral lenalidomide once daily on days 1-21. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also receive rituximab IV on days 15 and 22 of course 1 and on days 1 and 8 of course 2. Patients who do not achieve complete response after 2 courses of rituximab may receive up to 4 additional doses of rituximab once weekly for 4 weeks.

Blood samples are collected at baseline and after treatment for cytokine analysis.

After completion of study treatment, patients are followed at 30 days and then every 3 months thereafter.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: December 2024
• Est. primary completion date: April 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically* confirmed non-Hodgkin lymphoma, including one of the following subtypes:

• Grade 1, 2, or 3a (> 15 centroblasts per high-power field with centrocytes present) follicular lymphoma according to WHO criteria

• Small lymphocytic lymphoma

• NOTE: *Bone marrow biopsies as the sole means of diagnosis are not acceptable, but they may be submitted in conjunction with nodal biopsies or extra-nodal biopsies; fine-needle aspirates are not acceptable for diagnosis.

• At least one measurable lesion according to RECIST criteria

• Measurable lymphadenopathy to follow with serial exam and/or imaging

• Relapsed or refractory disease

• Must have evidence of disease progression during or after last treatment

• If previously treated with rituximab, must have disease progression within 6 months of last therapy OR if there was a prior response to rituximab, rituximab must not have been given within the past 6 months

• No evidence of CNS metastases

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Life expectancy > 3 months

• Absolute neutrophil count = 1,000/mm³

• Platelet count = 75,000/mm³

• Serum creatinine = 2.0 mg/dL

• Total bilirubin = 2.0 mg/dL

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective double method contraception for = 28 days before, during, and for = 28 days after completion of study therapy

• HIV negative

• Able to swallow lenalidomide

• Able to take aspirin (81 or 325 mg) daily or low molecular weight heparin as prophylactic anticoagulation

• No neuropathy = grade 2

• No known active hepatitis A, B, or C

• No other malignancies within the past 5 years except treated basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast

• No serious medical condition, laboratory abnormality, or psychiatric illness that would preclude the patient from signing the informed consent form

• No condition, including the presence of laboratory abnormalities, that would preclude study participation or confound the ability to interpret study data

• No known hypersensitivity to thalidomide or rituximab

• No development of erythema nodosum, if characterized by a desquamating rash while taking thalidomide or similar drugs

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• At least 4 weeks since prior anticancer therapy, including radiotherapy, hormonal therapy, or surgery

• More than 28 days since prior experimental drug or therapy

• No prior lenalidomide

• No other concurrent anticancer agents or treatments, including radiotherapy or thalidomide

• No other concurrent investigational agents

• No concurrent sargramostim (GM-CSF)

• No other concurrent antilymphoma therapy, including steroids (except for the treatment of hypersensitivity reactions)

Related Conditions & MeSH terms

• Lymphoma

Intervention

Biological:
• Rituximab
Injection for Intravenous Use, 375 mg/m2/wk x 4 weeks, to begin Cycle 1, Day 15.

Drug:
• Lenalidomide
Supplied as 5mg capsules; Dosage: 20 mg daily, days 1-21 of a 28 day cycle, to begin Day 1 of cycle 1 and continue until disease progression.

Locations

Country	Name	City	State
United States	University of California Davis Cancer Center	Sacramento	California

Sponsors (2)

Lead Sponsor	Collaborator
University of California, Davis	Celgene

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response, as defined by complete response (CR), near CR, partial response, or stable disease at 4 months	Responses will be assessed by the Revised Working Group Response Criteria for Malignant Lymphoma. A complete response is the complete disappearance of all detectable clinical evidence of disease and disease-related symptoms if present before therapy. A partial response is regression of measurable disease and no new sites of disease. Stable disease is failure to attain a complete response/partial response or progressive disease.	4 months
Secondary	Time to disease progression	Time to progression will be measured as the time from when the patient started treatment to the time the patient is first recorded as having disease progression, or the date of death if the patient dies due to causes other than disease progression	Up to two years
Secondary	Tolerability (type, frequency, severity, and relationship of adverse events to study treatment as assessed by NCI CTCAE v3.0)		Up to two years
Secondary	Duration of response	The duration of response is measured from the time measurement criteria are met for complete response/partial response(whichever status is recorded first) until the first date that recurrent or progressive disease is objectively documented (taking as reference for progressive disease the smallest measurements recorded since the treatment started).; The duration of response is measured from the time measurement criteria are first met for complete response until the first date that recurrent disease is objectively documented.	Up to two years
Secondary	Overall survival	Overall survival wil be measured as the time from start of treatment to the date of death or the last date the patient was known to be alive	Up to two years