Study to Evaluate Two Lenalidomide Dose Regimens With Low Dose Dexamethasone for the Treatment Relapsed Multiple Myeloma

NCT01380106 | Completed Phase 2 Results DMC

• 1 other identifier: RV-MM-PI-0345
• Study Type: interventional
• Target: 33
• Locations: 1 country
• Sites: 7

Brief Summary

This is a research study to evaluate two different Lenalidomide doses (15 mg vs. 25 mg) in combination with low dose dexamethasone in patients with relapsed multiple myeloma. The investigators propose to use the need for dose reduction as a criterion to judge tolerability from various causes. In the veteran population which predominantly is in the older age category with number of co-morbidities, a lower dose regimen may be safer and advantageous. This study expects to enroll approximately 80 subjects from participating VA sites across the nation. The investigators will evaluate the safety of the two dose regimens by comparing frequency of dose reductions. The investigators will also measure how long the responses last with each dose. Lenalidomide is approved by the Food and Drug Administration (FDA) for the treatment of specific types of myelodysplastic syndrome (MDS) and in combination with dexamethasone for patients with multiple myeloma (MM) who have received at least 1 prior therapy. MDS and MM are cancers of the blood. It is currently being tested in a variety of cancer conditions. In this case it is considered experimental. At the time of enrollment, one-half of the subjects will be chosen at random to receive the 15 mg Lenalidomide dose and the other half will take the 25 mg dose regimen of Lenalidomide. Depending on lenalidomide treatment assignment, subjects will receive either 15 mg p.o. q.d. or 25 mg p.o. q.d. for days 1-21 of a 28 day cycle. In addition, dexamethasone (40 mg) will be added once a week (Days 1, 8, 15 and 22) to the Lenalidomide regimen, with a dose reduction on the same schedule if the patient cannot tolerate the higher dose of dexamethasone. ASA (81 or 325mg) will be given daily for anticoagulation prophylaxis. Patients intolerant to ASA may use low molecular weight heparin. Lovenox is recommended. Coumadin will be allowed provided the patient is fully anticoagulate with INR 2.0 to 2.5.

Conditions

Multiple Myeloma

Keywords

Multiple myeloma; Relapsed; Revlimid

Outcome Measures

Primary Outcomes (2)

• Serious Adverse Events

  Type, frequency, severity and timing of adverse events and their relationship to combination therapy with lenalidomide plus dexamethasone. SAE Grade 3 indicates a severe or medically significant but not immediately life threatening; hospitalization or prolongation of hospitalization; disabling; limiting self care ADL SAE Grade 4 indicates a life-threatening consequences; urgent intervention indicated. SAE Grade 5 Death related to AE.

  Data was collected for each subject for the duration of the participation in the study, ranging between 75 to 475 days.

• Duration Until Best Response (at Least MR or Minimal Response)

  Number of days between the first day of the first cycle to best M-protein response, at least Minimal Response or higher (Partial Response, Very Good Partial Response, near Complete Response, Complete Response).

  Data was collected for each subject for the duration of the participation in the study, ranging between 75 to 475 days.

Study Arms (2)

Lenalidomide 25mg

ACTIVE COMPARATOR

Subjects will receive oral lenalidomide 25mg once daily for days 1-21 out of a 28 cycle

Drug: Lenalidomide 25mg

Lenalidomide 15mg

ACTIVE COMPARATOR

Subjects will receive oral lenalidomide 15mg once daily for days 1-21 out of a 28 cycle

Drug: Lenalidomide 15mg

Interventions

Lenalidomide 15mg DRUG

Subjects will receive oral lenalidomide 15 mg once daily for 1-21 of a 28 day cycle.

Also known as: REVLIMID®

Lenalidomide 15mg

Lenalidomide 25mg DRUG

Subjects will receive oral lenalidomide 25mg once daily for days 1-21 out of a 28 cycle

Also known as: REVLIMID®

Lenalidomide 25mg

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Previously diagnosed with multiple myeloma.
• Must have relapsed or refractory disease (refractory is defined as progression during treatment or within 60 days after the completion of treatment) requiring 2nd or 3rd line therapy
• Patients may have received lenalidomide and/or dexamethasone
• Patients must have measurable disease:
• Serum monoclonal protein \>0.5g/dL and/or 0.2g/24hr urine light chain excretion
• Patients with lower M-protein values or non-secretory myeloma will be eligible if measurable disease can be established, such as serum FreeliteTM chain ratio \>5x ULN, measurable soft tissue plasmacytoma \>2cm by either physical exam and/or applicable radiographs (i.e. MRI, CT-scan) and/or bone marrow involvement \>30%
• Age \>=18 years at the time of consent.
• All necessary baseline studies for determining eligibility must be obtained within 14 days prior to enrollment. Serum pregnancy tests (sensitivity of at least 25 mIU/mL), for females of childbearing potential (WCBP) must be completed. The first test must be performed within 10-14 days, and the second test within 24 hours prior to initiation of lenalidomide.
• Pre-study ECOG performance status 0-2. Patients with lower performance status based solely on bone pain will be eligible.
• Adequate liver functions: AST and ALT =\< 3xULN, alkaline phosphatase =\< 3.0x ULN, except if attributed to tumor, and bilirubin =\< 2xULN.
• Have Amylase =\< 2.5x ULN
• Able to adhere to the study visit schedule and other protocol requirements
• Must understand and voluntarily sign an informed consent document.
• Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL 10 - 14 days prior to and again within 24 hours of starting lenalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 4 weeks before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree not to father a child and agree to use a condom if his partner is of child bearing potential. All patients must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure.
• All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist®. All counseling will be done through RevAssist®.

You may not qualify if:

• Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
• Pregnant or breast feeding females.(Lactating females must agree not to breast feed while taking lenalidomide).
• Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.
• Renal insufficiency of creatinine clearance \<40mL/min
• Known hypersensitivity to thalidomide or lenalidomide.
• Development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs.
• Concurrent use of other anti-cancer agents or treatments.
• Known seropositive for an active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV). Patients who are seropositive because of hepatitis B virus vaccine are eligible.
• Has hemoglobin \<8.0g/dL. The use of transfusion with pRBC to correct anemia and meet eligibility criteria will not be allowed.
• Has an absolute neutrophil count \<1.0x10\^9/L within 14 days before enrollment
• Peripheral neuropathy of grade \>=3. Patients with painful grade 2 neuropathy are also excluded
• Has platelet count \<75x10\^9/L within 14 days before enrollment.
• Plasma cell leukemia at time of study entry.

Sponsors & Collaborators

• Boston VA Research Institute, Inc.: lead
• Celgene Corporation: collaborator
• Kansas City Veteran Affairs Medical Center: collaborator
• VA Pittsburgh Healthcare System: collaborator
• VA Greater Los Angeles Healthcare System: collaborator
• Michael E. DeBakey VA Medical Center: collaborator
• Edward Hines Jr. VA Hospital: collaborator

Study Sites (7)

Central Arkansas Veterans Healthcare System

Little Rock, Arkansas, 72205, United States

Location

West Los Angeles VA Medical Center

Los Angeles, California, 90073, United States

Location

Edward Hines Jr VA Hospital

Hines, Illinois, 60141, United States

Location

VA Boston Healthcare System

Jamaica Plain, Massachusetts, 02130, United States

Location

Kansas City VA Medical Center

Kansas City, Missouri, 64128, United States

Location

Pittsburgh VA Medical Center

Pittsburgh, Pennsylvania, 15240, United States

Location

Houston VA Medical Center

Houston, Texas, 77030, United States

Location

MeSH Terms

Conditions

Multiple Myeloma; Recurrence

Interventions

Lenalidomide

Condition Hierarchy (Ancestors)

Neoplasms, Plasma Cell; Neoplasms by Histologic Type; Neoplasms; Hemostatic Disorders; Vascular Diseases; Cardiovascular Diseases; Paraproteinemias; Blood Protein Disorders; Hematologic Diseases; Hemic and Lymphatic Diseases; Hemorrhagic Disorders; Lymphoproliferative Disorders; Immunoproliferative Disorders; Immune System Diseases; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Phthalimides; Phthalic Acids; Acids, Carbocyclic; Carboxylic Acids; Organic Chemicals; Piperidones; Piperidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Isoindoles; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring

Results Point of Contact

• Title: Nikhil C. Munshi, M.D.
• Organization: Boston VA Research Institute, Inc.

nikhil.munshi@dfci.harvard.edu

6176325607

Study Officials

• Nikhil C Munshi, M.D.

  Boston VA Research Institute, Inc.

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator -- Coordinating site

Study Record Dates

• First Submitted: June 22, 2011
• First Posted: June 27, 2011
• Study Start: August 1, 2010
• Primary Completion: September 11, 2017
• Study Completion: September 11, 2017
• Last Updated: January 25, 2021
• Results First Posted: January 25, 2021

Record last verified: 2021-01

Data Sharing

• IPD Sharing: Will not share

Locations

US (7)