Lenalidomide in Treating Patients With High-Risk Chronic Lymphocytic Leukemia

National Cancer Institute (NCI)

Status and phase: Withdrawn; Phase 2

Conditions: Stage IV Chronic Lymphocytic Leukemia; Stage III Chronic Lymphocytic Leukemia; Chronic Lymphocytic Leukemia

Treatments: Other: Diagnostic Laboratory Biomarker Analysis; Drug: Lenalidomide

Study type: Interventional

Funder types: NIH

Identifiers

NCT01271283

P30CA016056 (U.S. NIH Grant/Contract)

RPCI # I 174910 (Other Identifier)

8254 (Other Identifier)

CDR0000692070

NCI-2011-02568 (Registry Identifier)

Details and patient eligibility

About

This phase II clinical trial is studying how well lenalidomide works in treating patients with high-risk chronic lymphocytic leukemia. Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing.

Full description

PRIMARY OBJECTIVES:

I. To determine the time to progression in patients with high-risk chronic lymphocytic leukemia (CLL) treated with lenalidomide.

SECONDARY OBJECTIVES:

I. To determine the clinical response (complete and partial response) in treatment-naïve patients with high-risk CLL treated with single-agent lenalidomide.

II. To determine the incidence of immune-mediated flare reaction. III. To determine the toxicity profile of single-agent lenalidomide in previously untreated patients with high-risk CLL.

IV. To conduct correlative studies in bone marrow, peripheral blood, and/or lymph nodes of patients treated with lenalidomide.

OUTLINE:

Patients receive oral lenalidomide once daily on days 1-21. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity. Patients who achieve complete response (by morphological criteria but have persistent minimal residual disease by molecular criteria) or partial response may continue treatment beyond 8 courses. Patients may undergo bone marrow, peripheral blood, and/or lymph node sample collection at baseline and periodically during study for correlative studies.

After completion of study therapy, patients are followed up every 3 months for a maximum of 5 years.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Definitive diagnosis of B-cell chronic lymphocytic leukemia (B-CLL) as defined by the International Workshop on Chronic Lymphocytic Leukemia (IWCLL) criteria

  • Must have high-risk B-CLL as defined by ≥ one of the following:

    • High-risk cytogenetics (either 17p deletion and/or 11q deletion)
    • Unmutated immunoglobulin heavy chain gene rearrangement

  • Zap-70 and CD38 expression on leukemic cells will not be used as eligibility criteria for enrollment into the clinical trial

• No prior treatment for the management of B-CLL

• Patients must have B-CLL requiring therapy as defined by the IWCLL criteria

• Must have measurable disease meeting one of the following criteria:

  • Absolute lymphocyte count > 5,000/μL
  • Measurable lymphadenopathy or organomegaly

• No tumor lysis syndrome (TLS) by Cairo-Bishop definition

  • Patients with correction of electrolyte abnormalities allowed

• ECOG performance status 0-2

• ANC ≥ 1,500/mm³

• Platelet count ≥ 75,000/mm³

• Creatinine clearance ≥ 30 mL/min

• Total bilirubin ≤ 1.5 times upper limit of normal (ULN)

• AST and ALT ≤ 3 times ULN (≤ 5 times ULN if hepatic metastases are present)

• Uric acid normal

  • Patients with elevated uric acid allowed provided it is corrected with appropriate pharmacologic measures

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must commit to continued abstinence from heterosexual intercourse or use 2 acceptable methods of contraception (1 highly effective method and 1 additional effective method) ≥ 28 days prior to, during, and for ≥ 28 days after discontinuing lenalidomide

• Able to adhere to the study visit schedule and other protocol requirements

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

• No condition, including the presence of laboratory abnormalities, that would place the patient at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study

• No known hypersensitivity to thalidomide or lenalidomide

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

• No history of any other cancer except non-melanoma skin cancer or carcinoma in-situ of the cervix or cancer for which the patient is in complete remission and off therapy for > 3 years

• No cardiac arrest within the past 6 months

• No known history of hepatitis B infection, positive hepatitis B surface antigen, or positive hepatitis C antibody

• No other concurrent anti-cancer agents or treatments

• More than 28 days since any prior experimental drug or therapy

• Aspirin (81 or 325 mg) or warfarin sodium daily as prophylactic anticoagulation required

• No prior lenalidomide

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Arm I

Experimental group

Description:

Patients receive oral lenalidomide once daily on days 1-21. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity. Patients who achieve complete response (by morphological criteria but have persistent minimal residual disease by molecular criteria) or partial response may continue treatment beyond 8 courses. Patients may undergo bone marrow, peripheral blood, and/or lymph node sample collection at baseline and periodically during study for correlative studies.

Treatment:

Drug: Lenalidomide

Other: Diagnostic Laboratory Biomarker Analysis