Comparison of 25mg Versus 5 mg Lenalidomide as Maintenance Therapy in Patients With Multiple Myeloma

Inclusion Criteria: * Signed informed consent form * Age 18-75 years * Able to adhere to the study visit schedule and other protocol requirements * Patients with multiple myeloma who have received high-dose therapy and autologous stem cell transplantation as first-line therapy within the last 90 - 120 days and have not shown progressive disease afterwards. * Patients may have received up to 6 cycles of prior induction therapy and up to 2 cycles of prior mobilisation chemotherapy. A bortezomib or thalidomide induction therapy is allowed. Patients may also have received prior radiation therapy * Measurable levels of myeloma paraprotein in serum (\>0.5 g/dL) or urine (\>0.2 g/24hours) or measurable free light chains (FLC) in serum (\>50 mg/l) with an abnormal FLC ratio must be documented at the time of first diagnosis. * ECOG performance status = 2 at study entry * Laboratory and functional test results within these ranges: * ANC ≥ 1,000/μL * Platelet count ≥ 100,000/μL * Total bilirubin 2.5 mg/dL * AST (SGOT) and ALT (SGPT) 3 x ULN * Patients with impaired renal function can be included * The patient must be able to adhere to the pregnancy precautions * Disease free of prior malignancies for 5 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in situ" of the cervix or breast Exclusion Criteria: * 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 * Any condition or laboratory abnormality which places the subject at an unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study * Known allergic/hypersensitivity reaction to thalidomide, lenalidomide or any components of the treatment * Any cutaneous grade ≥ 3 adverse reaction (for example desquamating rash) while taking thalidomide or similar drugs * Any prior use of lenalidomide * Known positive for HIV or active infectious hepatitis, type A, B or C