Lenalidomide And Rituximab as Maintenance Therapy in Treating Patients With B-Cell Non-Hodgkin Lymphoma

The study was originally intended to be Phase I/Phase II but it terminated early because of
toxicity of treatment and therefore never moved to the Phase II portion of the study.

PRIMARY OBJECTIVES: I. To establish the maximum tolerated dose (MTD) and safety of
lenalidomide in combination with rituximab in subjects with B-cell NHL following ASCT.
(Phase I) II. To evaluate the tolerability of maintenance therapy with lenalidomide and
rituximab after ASCT in subjects with B-cell NHL. (Phase II)

SECONDARY OBJECTIVES: I. To evaluate the progression-free survival of subjects with B-cell
NHL receiving maintenance therapy with lenalidomide and rituximab after ASCT. II. To examine
whether potential effects of lenalidomide and rituximab on progression-free survival after
ASCT, compared with historical controls, vary according to histologic subtype of B-cell NHL.
III. To correlate potential associations between peripheral blood levels of lymphocyte
subsets including NK, T, and B cells and progression-free survival after ASCT in enrolled
subjects. IV. To evaluate potential associations between progression-free survival after
ASCT and polymorphisms at position 158 of FCgammaRIIIa receptor in enrolled subjects.

OUTLINE: Patients receive oral lenalidomide once daily on days 1-21of all courses and
rituximab IV on day 1of courses 1, 3, 5, 7, 9, and 11. Treatment repeats every 28 days for
up to 12 courses in the absence of disease progression or unacceptable toxicity. After
completion of study treatment, patients are followed periodically for 2 years.

Inclusion Criteria:

- Understand and voluntarily sign an informed consent form

- Able to adhere to the study visit schedule and other protocol requirements

- Histologic diagnosis of CD20+ B-cell NHL including diffuse large B-cell lymphoma,
follicular lymphoma, mantle cell lymphoma and other B-cell lymphomas excluding
chronic lymphocytic leukemia

- Received high-dose chemotherapy with autologous stem cell transplantation (ASCT) from
42 to 128 days before enrollment with stable disease, partial response or complete
response following ASCT

- All previous cancer therapy, including radiation, hormonal therapy and surgery, must
have been discontinued at least 4 weeks prior to treatment in this study

- ECOG performance status of =< 2 at study entry; Karnofsky performance status of >=
70% at study entry

- Absolute neutrophil count >= 1,500/mm^3

- Platelet count >= 75,000/mm^3

- Serum creatinine =< 2.0 mg/dL

- Phase I subjects must have estimated or measured creatinine clearance >= 60 ml/min

- Phase II subjects must have estimated or measured creatinine clearance >= 30 ml/min

- Total bilirubin =< 1.5 mg/dL

- AST (SGOT) and ALT (SGPT) =< 2 x ULN or =< 5 x ULN if hepatic metastases are present

- Disease free of prior malignancies for >= 5 years with exception of currently treated
basal cell, squamous cell carcinoma of the skin, or carcinoma "insitu" of the cervix
or breast

- 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 prior to
and again within 24 hours of prescribing lenalidomide for cycle 1 (prescriptions must
be filled within 7 days)

- Must also 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

- Able to take aspirin (81 or 325 mg) daily as prophylactic anticoagulation (subjects
intolerant to ASA may use warfarin or low molecular weight heparin)

- All study participants must be registered into the mandatory RevAssist program, and
be willing and able to comply with the requirements of RevAssist

Exclusion Criteria:

- Any serious medical condition, laboratory abnormality, or psychiatric illness that in
the opinion of the investigator would prevent the subject from providing written
informed consent

- Pregnant or breast feeding females (lactating females must agree not to breast feed
while taking lenalidomide)

- Use of any other experimental drug or therapy within 28 days of baseline

- Known hypersensitivity to thalidomide

- The development of erythema nodosum if characterized by a desquamating rash while
taking thalidomide or similar drugs

- Known hypersensitivity to rituximab

- Concurrent use of other anti-cancer agents or treatments

- Known positive for HIV or infectious hepatitis, type B or C

- Residual grade 3 or grade 4 non-hematologic toxicity after ASCT

- Transfusion requirement (red blood cells or platelets) within 14 days prior to
baseline

- Use of hematopoietic growth factor (including filgrastim, pegfilgrastim,
sargramostim, erythropoietin, or darbepoetin) within 14 days prior to baseline

- Any other condition not defined above, including the presence of laboratory
abnormalities, which in the opinion of the investigator would place the subject at
unacceptable risk if he/she were to participate in the study, or would confound the
ability to interpret data from the study

- Prior use of lenalidomide either concurrently with rituximab or within 8 weeks
following a dose of rituximab

- Concomitant use of other anti-cancer therapies, including radiation, thalidomide, or
other investigational agents is not permitted while subjects are receiving protocol
therapy during the treatment phase of the study

- Corticosteroid therapy also is not permitted while subjects are receiving protocol
therapy during the treatment phase of the study