Overview

Lenalidomide, Cyclophosphamide, and Dexamethasone in Treating Patients With Primary Systemic Amyloidosis

Status:
Completed
Trial end date:
2012-06-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop plasma cells from growing. Drugs used in chemotherapy, such as cyclophosphamide and dexamethasone, work in different ways to stop the growth of plasma cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with cyclophosphamide and dexamethasone may be an effective treatment for primary systemic amyloidosis. PURPOSE: This phase II trial is studying how well giving lenalidomide together with cyclophosphamide and dexamethasone works in treating patients with primary systemic amyloidosis.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Mayo Clinic
Collaborator:
National Cancer Institute (NCI)
Treatments:
BB 1101
Cyclophosphamide
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Lenalidomide
Thalidomide
Criteria
DISEASE CHARACTERISTICS:

- Histochemical diagnosis of AL amyloidosis based on detection of green birefringent
material in Congo red-stained tissue specimens by polarizing microscopy

- Measurable disease, as defined by one of the following:

- Serum monoclonal protein ≥ 1.0 g by serum electrophoresis

- Urine monoclonal protein > 200 mg by 24-hour urine electrophoresis

- Serum immunoglobulin free light chain ≥ 10 mg/dL AND abnormal serum
immunoglobulin kappa to lambda free light chain ratio

- Symptomatic organ involvement with amyloid to justify therapy

- May include liver involvement, cardiac involvement, renal involvement, grade 1
peripheral neuropathy, or soft tissue involvement

- Must have more than skin purpura or carpal tunnel syndrome

- No amyloid-specific syndrome, such as carpal tunnel syndrome or skin purpura, as only
evidence of disease

- Vascular amyloid only in a bone marrow biopsy specimen or in a plasmacytoma is not
indicative of systemic amyloidosis

- No clinically overt multiple myeloma (i.e., monoclonal BMPC > 30%, bone lesions, or
hypercalcemia)

PATIENT CHARACTERISTICS:

- ECOG performance status 0-2

- ANC ≥ 1,000/μL

- Platelet count ≥ 75,000/μL

- Creatinine < 3.0 mg/dL

- Not pregnant

- Negative pregnancy test

- Fertile patients must use two acceptable methods of contraception for ≥ 28 days prior
to, during, and for ≥ 28 days after completion of study treatment

- No nursing during and for ≥ 28 days after completion of study treatment

- No blood, semen, or sperm donation during and for ≥ 28 days after completion of study
treatment

- No malignancies within the past 5 years except treated basal cell or squamous cell
carcinoma of the skin, or carcinoma "in situ" of the cervix or breast

- No neuropathy ≥ grade 2, defined as motor neuropathy (symptomatic weakness interfering
with function, but not interfering with activities of daily living [ADL]) or sensory
neuropathy (sensory alteration or paresthesia [including tingling], interfering with
function, but not interfering with ADL)

- No uncontrolled infection

- No syncope within the past 30 days

- No known hypersensitivity to thalidomide, including desquamating rash with thalidomide
in the past

- No known seropositivity for HIV

- No active hepatitis A, B, or C

- No New York Heart Association class III or IV heart disease

- No venous thromboembolic event within the past 42 days

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

PRIOR CONCURRENT THERAPY:

- No prior lenalidomide

- More than 2 weeks since prior and no other concurrent anticancer agents or treatments

- More than 4 weeks since prior experimental agents

- No other concurrent corticosteroids except chronic steroids (maximum dose 20 mg/day of
prednisone equivalent) for disorders other than amyloidosis (e.g., adrenal
insufficiency or rheumatoid arthritis)