Non Hodgkin Lymphoma Clinical Trial
Oblimersen Sodium and Rituximab in Treating Patients With Recurrent B-cell Non-Hodgkin Lymphoma
Summary
The goal of this clinical research study is to learn if the combination of oblimersen sodium and rituximab can help to shrink or slow the growth of the tumor in patients with B-cell non-Hodgkin's lymphoma who have not responded to earlier treatment. Oblimersen Sodium is an investigational drug. The safety of this combination treatment will also be studied
Full Description
PRIMARY OBJECTIVES:
I. To determine the therapeutic efficacy and toxicity of G3139 (oblimersen sodium) and Rituximab in patients with recurrent B-cell NHL.
SECONDARY OBJECTIVES:
I. To determine the effect of G3139 and Rituximab on the level of Bcl-2 expression.
II. The secondary objective of this study is to evaluate the effect of G3139 and Rituximab on Bcl-2 protein gene expression.
OUTLINE:
Patients receive oblimersen sodium intravenously (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.
After completion of study treatment, patients are followed up every 3 months.
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
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There is 1 Location for this study
Houston Texas, 77030, United States
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