| Eligibility |
Inclusion Criteria:
- Age 18 years and = 80 years
- High risk smoldering myeloma, which is untreated, as defined by either of the two
following criteria:
1. Presence of any two of the following: Serum M spike > 2 gm/dL OR an involved to
uninvolved free light chain (FLC) ratio > 20 OR bone marrow PC% > 20%
2. Total score of 9 or above using the following scoring system:
FLC Ratio >10-25 = 2 >25-40 = 3 > 40 = 5
Serum M Protein (g/dL) >1.5-3 = 3 >3 = 4
BMPC% >15-20 = 2 >20-30 = 3 >30-40 = 5 >40 = 6
FISH abnormality (t(4,14), t(14,16), 1q gain, or del13q = 2
- The following laboratory values obtained 14 days prior to registration.
- Calculated creatinine clearance (using Cockcroft-Gault equation below)* = 30 mL/min
- Absolute neutrophil count (ANC) = 1000/mm3 (without the use of growth factors)
- Platelet count = 75000/mm3
- Hemoglobin =8.0 g/dL
- Total bilirubin = 1.5 x upper limit of normal (ULN)
- alanine aminotransferase (ALT) and aspartate aminotransferase (AST) = 3 x ULN
- left ventricular ejection fraction (LVEF) = 40%
- LVEF = 40%
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1 (Appendix
VII)
- Previously untreated.
- Provide informed written consent.
- Negative pregnancy test done =14 days prior to cycle 1 day 1, for women of
childbearing potential only.
- All study participants must be registered into the mandatory Revlimid Risk Evaluation
and Mitigation Strategy (REMS®) program and be willing and able to comply with the
requirements of the REMS® program.
- Females of reproductive potential must adhere to the scheduled pregnancy testing as
required in the Revlimid REMS® program.
- Willing to follow strict birth control measures as outlined in the protocol.
Female subjects: If they are of childbearing potential, agree to one of the following:
- Practice 2 effective methods of contraception, at the same time, from the time of
signing the informed consent form through 90 days after the last dose of trial drug,
AND must also adhere to the guidelines of any treatment-specific pregnancy prevention
program, if applicable, OR
- Agree to practice true abstinence when this is in line with the preferred and usual
lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation,
symptothermal, post-ovulation methods] and withdrawal are not acceptable methods of
contraception.)
Male subjects: even if surgically sterilized (i.e., status post-vasectomy), must agree to
one of the following:
- Agree to practice effective barrier contraception during the entire trial treatment
period and through 90 days after the last dose of trial drug, OR
- Must also adhere to the guidelines of any treatment-specific pregnancy prevention
program, if applicable, OR
- Agree to practice true abstinence when this is in line with the preferred and usual
lifestyle of the subject. (Periodic abstinence (e.g., calendar, ovulation,
symptothermal, post-ovulation methods] and withdrawal are not acceptable methods of
contraception).
- Willing to return to enrolling institution for follow-up during the Active
Treatment Phase of the trial.
- Male subjects must agree not to donate sperm for at least 90 days after the last
dose of study treatment.
- Willing to provide samples for planned research
- Life expectancy > 6 months
- Able to take aspirin (325 mg) daily as prophylactic anticoagulation. Subjects
intolerant to aspirin may use warfarin or low dose molecular weight heparin,
novel oral anticoagulants, or low dose molecular weight heparin
Exclusion Criteria:
- monoclonal gammopathy of undetermined significance (MGUS), standard risk smoldering
myeloma, active myeloma by current IMWG definition, light chain amyloidosis with organ
involvement or patients with extramedullary disease.
- Diagnosed or treated for another malignancy = 2 years before trial enrollment or
previously diagnosed with another malignancy and have any evidence of residual
disease. NOTE: Subjects with nonmelanoma skin cancer or carcinoma in situ of any type
are not excluded if they have undergone complete resection.
- If any of the following exist at screening, subject will not be eligible for trial
because this trial involves an investigational agent whose genotoxic, mutagenic and
teratogenic effects on the developing fetus and newborn are unknown:
- Pregnant women
- Nursing women
- Men or women of childbearing potential who are unwilling to employ adequate
contraception (per protocol)
- Other co-morbidity which would interfere with subject's ability to participate in
trial, e.g. uncontrolled infection, uncompensated heart or lung disease.
- Other concurrent chemotherapy, or any ancillary therapy considered investigational.
NOTE: Bisphosphonates are considered to be supportive care rather than therapy, and
are thus allowed while on protocol treatment.
- Peripheral neuropathy = Grade 3 on clinical examination or grade 2 with pain within 30
days prior to C1D1.
- Major surgery =14 days prior to C1D1.
- Evidence of current uncontrolled cardiovascular conditions, including hypertension,
cardiac arrhythmias, congestive heart failure, unstable angina, or myocardial
infarction within the past 6 months. Note: Prior to trial entry, any ECG abnormality
at screening must be documented by the investigator as not medically relevant.
- New York Heart Association (NYHA) II, III, IV heart failure
- Known human immunodeficiency virus (HIV) positive.
- Seropositive for hepatitis B (defined by a positive test for hepatitis B surface
antigen [HBsAg]). Subjects with resolved infection (ie., subjects who are HBsAg
negative but positive for antibodies to hepatitis B core antigen [anti-HBc] and/or
antibodies to hepatitis B surface antigen [anti-HBs]) must be screened using real-time
polymerase chain reaction (PCR) measurement of hepatitis B virus (HBV) DNA levels.
Those who are PCR positive will be excluded. EXCEPTION: subjects with serologic
findings suggestive of HBV vaccination (anti-HBs positivity as the only serologic
marker) AND a known history of prior HBV vaccination, do not need to be tested for HBV
DNA by PCR.
- Known or suspected active hepatitis C infection.
- Any medical or psychiatric illness that could, in the investigator's opinion,
potentially interfere with the completion of treatment according to this protocol.
- Prior radiation therapy for bony lesions or plasmacytomas
- Known allergies, hypersensitivity, or intolerance to corticosteroids, monoclonal
antibodies or human proteins, or their excipients (refer to respective package inserts
or Investigator's Brochure), or known sensitivity to mammalian-derived products. Known
allergies, hypersensitivity, or intolerance to trial drugs.
- Inability to comply with protocol/procedures.
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