DARA RVD For High Risk SMM

Inclusion Criteria

• •Age ≥ 18 years.
• •Must meet criteria of high-risk smoldering MM as described with one of the below criteria:
• •* Bone marrow clonal plasma cells ≥10% and any one or more of the following:
• •* Serum M protein ≥3.0 gm/dL
• •* Immunoparesis with reduction of two uninvolved immunoglobulin isotypes
• •* Serum involved/uninvolved free light chain ratio ≥8 (but less than 100)
• •* Free Light Chain Smoldering Myeloma patients are not excluded
• •* Progressive increase in M protein level (Evolving type of SMM)\*\*\* Increase in serum monoclonal protein by ≥10% on two successive evaluations within a 6-month period
• •* Bone marrow clonal plasma cells 50-60%
• •* Abnormal plasma cell immunophenotype (≥95% of bone marrow plasma cells are clonal) and reduction of one or more uninvolved immunoglobulin isotypes
• •* High Risk FISH defined as any one or several of the following: t(4;14), t(14;16), t(14;20), del 17p or 1q gain
• •* MRI with diffuse abnormalities or 1 focal lesion (≥5mm)
• •* PET-CT with one focal lesion (≥5mm) with increased uptake without underlying osteolytic bone destruction
• •* OR High-risk per IMWG/Mayo 2018 "20-2-20" Criteria (at least 2 of the following)
• •* Bone marrow plasmacytosis ≥20%
• •* ≥ 2g/dl M protein
• •* 20 involved: uninvolved serum free light chain ratio
• •No evidence of CRAB criteria\* or new criteria of active MM which including the following:
• •* Increased calcium levels: Corrected serum calcium \>0.25 mmol/L(\>1mg/dL) above the upper limit of normal or \>2.75 mmol/L (\>11mg/dL);
• •* Renal insufficiency (attributable to myeloma);
• •* Anemia (Hgb 2g/dL below the lower limit of normal or \<10g/dL);
• •* Bone lesions (lytic lesions or generalized osteoporosis with compression fractures)
• •* No evidence of the following new criteria for active MM including the following:
• •* Bone marrow plasma cells \>60%
• •* Serum involved/uninvolved FLC ratio ≥100
• •* MRI with more than one focal lesion
• •* Participants with CRAB criteria that are attributable to conditions other than the disease under study may be eligible after discussion with the Sponsor Investigator
• •ECOG Performance Status (PS) 0, 1, or 2 (Appendix A)
• •The following laboratory values obtained ≤ 28 days prior to registration:
• •* ANC ≥1000/ µL
• •* PLT ≥ 50,000/ µL
• •* Total bilirubin ≤ 2.0 mg/dL (If total is elevated check direct and if normal patient is eligible.)
• •* AST≤ 3 x institutional upper limit of normal (ULN)
• •* ALT ≤ 3 x institutional upper limit of normal (ULN)
• •* Estimated creatinine clearance≥ 60mL/min or a creatinine ≤ 2.2 mg/dL
• •Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.
• •Females of childbearing potential\* must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days and again within 24 hours prior to prescribing lenalidomide for Cycle 1 (prescriptions must be filled within 7 days as required by Revlimid REMS®) 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 28 days before she starts taking lenalidomide.
• •\-- A female of childbearing potential is a sexually mature female who: has not undergone a hysterectomy (the surgical removal of the uterus) or bilateral oophorectomy (the surgical removal of both ovaries) or has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time during the preceding 24 consecutive months)
• •All study participants must be registered into the mandatory Revlimid REMS® program and be willing and able to comply with the requirements of the REMS® program.
• •Females of child-bearing potential must adhere to the scheduled pregnancy testing as required in the Revlimid REMS® program.
• •Men must agree to use a latex condom during sexual contact with a female of childbearing potential even if they have had a successful vasectomy
• •Detectable clonality sequence by next generation sequencing using clonoSEQ assay to allow for minimal residual disease measurement
• •Ability to understand and the willingness to sign a written informed consent.