Oblimersen Sodium and Rituximab in Treating Patients With Recurrent B-cell Non-Hodgkin Lymphoma
Cutaneous B-cell Non-Hodgkin Lymphoma, Extranodal Marginal Zone B-cell Lymphoma of Mucosa-associated Lymphoid Tissue, Intraocular Lymphoma
About this trial
This is an interventional treatment trial for Cutaneous B-cell Non-Hodgkin Lymphoma
Eligibility Criteria
Inclusion Criteria: Must have recurrent B-cell NHL and measurable disease No anti-lymphoma therapy within the past 4 weeks Must have a good performance status (less than or equal to 2 Zubrod, greater than or equal to 60 Karnofsky) Absolute neutrophil count (ANC) greater than or equal to 1,000 Platelets greater than or equal to 75,000 Hemoglobin greater than or equal to 10 g/dL Bilirubin less than or equal to 1.5 mg/dL Serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvate transaminase (SGPT) less than or equal to 2 times upper limit of laboratory normals Alkaline phosphatase less than or equal to 2 times upper limit of laboratory normals Serum creatinine less than or equal to 1.8 mg/dL Must sign a consent form, and must have a life expectancy of greater than 12 weeks No more than 3 prior chemotherapy regimens Patients who are either Rituximab naive, have previously responded to Rituximab, or are refractory to Rituximab used alone or in combination with chemotherapy Exclusion Criteria: Human immunodeficiency virus (HIV) positive Active infection or history of opportunistic infections Pregnant women and women of childbearing age who are not practicing adequate contraception; men who are not willing to use an effective method of contraception History of second cancer (except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer or other cancer for which the patient has been disease-free for 5 or more years) Active autoimmune disease Other significant medical diseases Patients with chronic lymphocytic leukemia (CLL) Prior exposure to G3139
Sites / Locations
- M D Anderson Cancer Center
Arms of the Study
Arm 1
Experimental
Treatment (oblimersen sodium and monoclonal antibody therapy)
Patients receive oblimersen sodium IV continuously on days 1-7, 15-21, and 29-35 and rituximab IV over 4-6 hours on days 3, 8, 15, 22, 29, and 36. Patients achieving stable disease or objective response may receive one additional course of treatment.