Lenalidomide (Revlimid®, CC-5013) in Subjects With Relapsed or Refractory Indolent Non-Hodgkin's Lymphoma

NCT ID: NCT00179673

Last Updated: 2025-05-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-06-30
• Study Completion Date: 2008-04-30

Brief Summary

Subjects who qualify will receive lenalidomide daily on days 1-21 of every 28-day cycle. Treatment will continue for up to 52 weeks or until disease progression; subjects who achieve a Complete Response (CR) will receive an additional 2 cycles of treatment prior to discontinuation. Subjects will be followed for progression free survival following discontinuation from the treatment phase

Conditions

Non-Hodgkins Lymphoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Lenalidomide

Participants received single-agent lenalidomide 25 mg orally once daily on Days 1 to 21 of every 28-day cycle for up to 52 weeks or until disease progression developed.

Group Type: EXPERIMENTAL

Lenalidomide

Intervention Type: DRUG

Interventions

Lenalidomide

Intervention Type: DRUG

Other Intervention Names

Revlimid; CC-5013

Eligibility Criteria

Inclusion Criteria

1. Understand and voluntarily sign an informed consent form.

2. Age greater than or equal to 18 years at the time of signing the informed consent form

3. Able to adhere to the study visit schedule and other protocol requirements

4. Biopsy-proven non-Hodgkin's lymphoma

5. Indolent lymphoma the following histologies are acceptable: a. Follicular center lymphoma, grades 1, 2; b. Extranodal marginal zone B-cell lymphoma of Mucosa associated lymphoid tissue (MALT) type, c. Nodal marginal zone B-cell lymphoma d. Splenic marginal zone B-cell lymphoma, e. Small lymphocytic lymphoma (SLL), f. Lymphoplasmacytoid lymphoma

6. Relapsed or refractory to previous therapy for lymphoma. Participants must have received at least one prior treatment regimen such as radiation, immunotherapy, chemotherapy, or radioimmunotherapy, and be ineligible or unwilling to undergo an autologous stem cell transplant. There is no limit on the number of prior therapies

7. Participants must have measurable disease on cross sectional imaging that is at least 2 cm in the longest diameter

8. Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2.

9. Women of childbearing potential (WCBP) must have a negative serum or urine pregnancy test within 7 days of starting study drug. In addition, sexually active WCBP must agree to use adequate contraceptive methods (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomized partner) while on study drug.

Exclusion Criteria

1. Any of the following laboratory abnormalities

1. Absolute neutrophil count (ANC) <1,500 cells/mm^3 (1.5 x 10^9/L)

2. Platelet count <100,000/mm^3 (100 x 10^9/L)

3. Serum creatinine >2.5 mg/dL (221 mmol/L)

4. Serum Serum glutamic oxaloacetic transaminase (SGOT)/aspartate aminotransferase (AST) or serum glutamic-pyruvic transaminase (SGPT)/alanine aminotransferase (ALT) >5.0 x upper limit of normal (ULN)

5. Serum total bilirubin >2.0 mg/dL (34 mmol/L)

2. Any condition, including the presence of laboratory abnormalities, which places the participant at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.

3. All participants with Central Nervous System (CNS) disease with the exception of those subjects whose CNS disease has been treated with chemotherapy, radiotherapy or surgery and remains asymptomatic, with no active CNS disease, as shown by lumbar puncture, computerized tomography (CT) scan or Magnetic resonance imaging (MRI), for at least 6 months.

4. Prior history of malignancies other than non-Hodgkin's lymphoma (except for basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast) unless the participant has been free of the disease for > or equal to 1 year.

5. Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the participant from signing the informed consent form.

6. Known positive for human immunodeficiency virus (HIV).

7. Pregnant or lactating females.

8. Prior > or equal to grade 3 allergic reaction/hypersensitivity to thalidomide.

9. Prior > or equal to grade 3 rash or any desquamating (blistering) rash while taking thalidomide.

10. Prior use of lenalidomide.

11. Use of any standard or experimental anti-cancer drug therapy within 28 days of day 1 of study drug therapy.

12. Known active Hepatitis C.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Prologue Research International

INDUSTRY

Sponsor Role: collaborator

Celgene

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Mayo Clinic Scottsdale

Scottsdale, Arizona, United States

Alta Bates Cancer Center

Berkeley, California, United States

Pacific Coast Hematology/Oncology Medical Group, Onc.

Fountain Valley, California, United States

Rush University Medical Center

Chicago, Illinois, United States

Harvard University

Boston, Massachusetts, United States

Mayo Clinic

Rochester, Minnesota, United States

University of Nebraska

Omaha, Nebraska, United States

New York Medical Center, MBCCOP

The Bronx, New York, United States

Signal Point Hematology/Oncology

Middletown, Ohio, United States

Swedish Cancer Institute

Seattle, Washington, United States

Gunderson Clinic, Ltd.

La Crosse, Wisconsin, United States

BC Community Oncology Trialist

Burnaby, British Columbia, Canada

BC Community Oncology

North Vancouver, British Columbia, Canada

London Regional Cancer Program

London, Ontario, Canada

University of Saskatchewan

Saskatoon, Saskatchewan, Canada

Countries

United States; Canada

Other Identifiers

CC-5013-NHL-001

Identifier Type: -

Identifier Source: org_study_id