Phase
Condition
Lymphoma
Brain Tumor
Treatment
N/AClinical Study ID
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: All patients must have non-Hodgkin's lymphoma involving the brain, as demonstrated by CT orMRI and histologic confirmation by one of the following: A positive CSF cytology forlymphoma or a monoclonal lymphocyte population as defined by cell surface markers. A biopsy of the vitreous or uvea demonstrating non-Hodgkin's lymphoma. Brain biopsy. Patients must be HIV-1 negative. Patient must have left ventricular ejection fraction ≥ 50%. Patients must have no evidence of systemic lymphoma. This must be demonstrated by a CTscan of the chest, abdomen and pelvis prior to registration. Patients must have adequate bone marrow function (defined as peripheral leucocyte count >3000 cells/mm3 and platelet count > 100,000 cells/mm3), liver function (bilirubin < 2.0mg/%), and adequate renal function (serum creatinine < 1.5 mg/dl or creatinine clearance > 50cc/min/1.73M2). Men and women of reproductive potential must agree to use an acceptable method of birthcontrol during treatment and for six months after completion of treatment. Patients must be between 18 and 70years-old. Patients must sign an informed consent.
Exclusion
Exclusion Criteria: Prior cranial irradiation Other active primary malignancy. Pre-existing immunodeficiencysuch as renal transplant recipient. Prior treatment with chemotherapy for CNS lymphoma.
Study Design
Study Description
Connect with a study center
Nathional Medical Research Center for Hematology
Moscow, 125167
Russian FederationActive - Recruiting
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