18 to 65 years old
bone marrow transplant, leukemia, cancer
Drug study, Phase 1
History and Physical Blood and Urine tests X-ray or CT scan ECGs Bone marrow biopsies Study drug treatment Drug diaries
Understand and voluntarily sign an informed consent form
Age greater than or equal to 18 and less than or equal to 65 years
Able to adhere to the study visit schedule and other protocol requirements.
High risk acute myelogenous leukemia or high risk myelodysplastic syndrome status post allogeneic bone marrow transplant
ECOG performance status of less than or equal to 2
Disease free of other malignancies beside the AML or MDS for ≥ 2 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix or breast.
All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist®.
Females of childbearing potential (FCBP) 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 RevAssist) 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. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy.
Between 6 months to 8 months post transplant
Neutrophil count of ≥ 1.5 x 109/L
Platelet count ≥ 50 x 109/L
Calculated creatinine clearance ≥ 60ml/min by Cockcroft-Gault formula
Total bilirubin ≤1.5 x upper limit of normal
AST (SGOT) and ALT (SGPT) ≤ 3 x upper limit of normal
Patients are eligible to start on this protocol if they are between 6 months to 10 months post transplant.
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 level of acute graft versus host disease
Active, uncontrolled infection are not eligible for this study
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
Use of any other experimental drug or therapy within 28 days of baseline.
Known hypersensitivity to thalidomide
Development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drug
Known sero-positive for active viral infection with HI, hepatitis B virus (HBV) or hepatitis C virus (HCV)
Mixed chimerism (at 6 months post transplant will not be started on the protocol
Active AML or MDS at the time of the study are not eligible for this protocol
Not able to swallow the lenalidomide capsule as a whole are excluded from this study
Impaired gastrointestinal absorption
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