Lenalidomide and Low-dose Cyclophosphamide for MALT Lymphoma (LCMALT)

This is an interventional treatment trial for Antibiotics-unresponsive MALT Lymphoma focused on measuring Marginal zone B-cell lymphoma, Low-dose Cyclophosphamide, Lenalidomide Read More

Inclusion Criteria:

1. Histologically verified diagnosis of MALT lymphoma arising at any extranodal site
2. Diseases of extranodal MALT lymphoma 2.1 It does not initially respond to antibiotics or 2.2 It is refractory to or in first or greater relapse after prior radiotherapy and/ or chemotherapy and/or immunotherapy
3. Measurable or non-measurable lesions where the response is nevertheless evaluable by non-imaging means (e.g., gastric or bone marrow infiltrations)
4. Ann Arbor Stage I-IV
5. ECOG performance status of 0, 1 or 2
6. Age ≥ 18 years
7. Life expectancy of at least 3 months
8. Adequate haematological status: ANC (absolute neutrophil count [segmented + bands]) ≥1.0 x 109/L, platelet count ≥ 75 x 109/L , haemoglobin ≥8 g/dL.
9. Adequate cardiac, renal and liver function tests (serum creatinine < 2.0 mg/dl, ALT or AST < 2.5 x upper limit of normal range, alkaline phosphatase < 2.5 x upper limit of normal range, serum bilirubin < 2.0 mg/dl)
10. Patient must be willing and able to comply with the protocol for the entire study duration
11. Female patients of childbearing potential must agree to use, and be able to comply with, effective contraception and agree to have medically supervised pregnancy tests prior to starting the study treatment and during therapy
12. Male patients must agree to always use a condom during any sexual contact with females of reproductive potential and agree to not donate sperm while taking lenalidomide
13. Patient must agree to abstain from donating blood while taking study drug therapy
14. Patient must agree not to share study medication with another person and to return all unused study drug to the investigator

Exclusion Criteria:

1. Lymphoma histology other than MALT lymphoma or MALT lymphoma with a diffuse large cell lymphoma ("high grade lymphoma") component
2. Use of any investigational agent within 28 days prior to initiation of treatment
3. History of malignancy other than squamous cell carcinoma, basal cell carcinoma of the skin or carcinoma in situ of the uterine cervix or carcinoma in situ of the breast within the last 5 years unless in complete remission since at least 3 years
4. Dependency on red blood cell and/or platelet transfusions
5. Evidence of central nervous system involvement
6. A history of uncontrolled seizures, central nervous system disorders or psychiatric disability judged by the investigator to be clinically significant and adversely affecting compliance to study drugs
7. Severe peripheral polyneuropathy
8. Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) or myocardial infarction within the last 6 months and/or long QT-syndrome
9. HIV seropositivity
10. Presence of active opportunistic infections
11. Pregnancy or lactation
12. Uncontrolled diabetes mellitus
13. Pre-existing thromboembolic conditions at study entry
14. Known hypersensitivity to thalidomide or lenalidomide antibiotics
15. History of intolerance or hypersensitivity to aspirin