Lenalidomide After Donor Stem Cell Transplant and Bortezomib in Treating Patients With High Risk Multiple Myeloma

• Status: Terminated
• Trial end date: 2017-01-30
• Target enrollment: 0
• Participant gender: All

Summary

This phase I trial studies the side effects and best dose of lenalidomide after donor stem cell transplant and bortezomib in treating patients with high-risk multiple myeloma. Giving low doses of chemotherapy and total-body irradiation before a donor stem cell transplant helps stop the growth of cancer cells. It may also the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving a bortezomib at the time of transplant may stop this from happening. Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing. Giving lenalidomide after donor stem cell transplant may be an effective treatment for multiple myeloma.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Case Comprehensive Cancer Center
• Collaborator: National Cancer Institute (NCI)
• Treatments: Bortezomib; Cyclosporine; Cyclosporins; Fludarabine; Fludarabine phosphate; Lenalidomide; Mycophenolate mofetil; Mycophenolic Acid; Thalidomide; Vidarabine

Criteria

Inclusion Criteria:

• Symptomatic multiple myeloma by International Myeloma Working Group (IMWG) criteria according to the most recent updated version (International Myeloma Workshop [IMW] meeting in Paris 2011)

• Must have received at least 3 of the following classes of anti-myeloma agents either alone or in combination: glucocorticoids, immunomodulatory drugs including thalidomide, proteasome inhibitors, alkylating chemotherapy, or anthracyclines

• Must meet any of these criteria for high risk disease:

• Relapse or progressive disease according to uniform response criteria within 2 years after starting first-line therapy or within 2 years after autologous stem cell transplant

• Failure to achieve partial response (PR) within 6 months of staring first-line therapy

• Presence of high risk cytogenetic features (t(14;16), t(14;20), deletion 17p)

• Chromosome 14 translocations other than to chromosome 11

• Chromosome 1p deletion and 1q amplification

• MyPRS gene expression score equal or higher than 45.2

• High risk 70 gene expression profile (MyPRS GEP70TM)

• Any other high risk genetic profile that is determined by future IMWG consensus or by internal myeloma panel consensus; for the latter, any additional criteria will be submitted as an addendum

• Diagnosis with multiple myeloma between the ages of 18-50

• Must have achieved at least a minor response to any previous regimen according to adapted European Group for Blood and Marrow Transplantation (EBMT) criteria

• Must have suitable matched sibling or matched unrelated donor for stem cell source

• Must be transplant-eligible per institution guidelines

• Must have estimated glomerular filtration rate (eGFR) by Modification of Diet in Renal Disease (MDRD) formula or Cockroft-Gault formula of 50mL/min or higher

• All study participants must be registered into the mandatory Revlimid REMS® program, and be willing and able to comply with the requirements of Revlimid REMS®

• Females of childbearing potential must have negative serum or urine pregnancy test and use acceptable birth control methods

• Able to take aspirin daily as prophylactic anticoagulation (patients intolerant to acetylsalicylic acid [ASA] may use warfarin or low molecular weight heparin)

Exclusion Criteria:

Participants must not:

• Have known hypersensitivity to thalidomide or lenalidomide

• Have progressive disease at the time of transplant

• Uncontrolled concurrent significant medical or psychological co-morbidity

• Grade 3 peripheral neuropathy

• Known seropositive for or 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

• Be females who are pregnant

• Recent (within 3 years) history of other malignancies, excluding basal cell carcinoma or squamous cell carcinoma of the skin

• Be currently enrolled in another investigational treatment protocol