Non Hodgkin Lymphoma Clinical Trial
Zevalin® Followed by Rituxan® Maintenance in Previously Treated Low Grade Non-Hodgkin’s Lymphoma
The purpose of this study is to determine the safety and effectiveness of a treatment regimen using ZevalinÂ® plus RituxanÂ® for patients who have low grade Non-Hodgkin's Lymphoma (NHL) or relapsed Non-Hodgkin's lymphoma and have been previously treated. This study will use an experimental scheduling regimen. No chemotherapy will be used in this study.
The objective of this study is to determine overall response rate, event-free survival, time-to-progression, time-to-next-therapy, and freedom-from-relapse in patients with low-grade lymphoma in first or second relapse treated with Zevalin followed by 2 years of Rituxan maintenance therapy in a multicenter, community-based setting, as well as evaluate relative response rates in populations with and without prior rituximab therapy, in first versus second relapse, and with and without bulky (> 5 cm in greatest diameter) disease.
To meet the initial trial enrollment goal of 300 patients over two years, 42 total sites were activated. The study has subsequently closed to accrual. Currently 8 sites remain active to follow the 12 subjects enrolled in the past year.
Follicular non-Hodgkin's lymphoma including SLL in first or second relapse.
No anticancer therapy for three wks (six wks if nitrosourea or Mitomycin C); not rituximab refractory.
Age >= 18 years, not pregnant or lactating.
Expected survival >= 3 mths; PS 0, 1, or 2.
ANC >= 1,500/mm3, platelet counts >= 100,000/mm3.
Total bilirubin > 2.0 mg/dL, creatinine > 2.0 mg/dL.
Total lymphocyte count < 5,000/mm3 for SLL.
<25% bone marrow involvement with lymphoma.
Prior ABMT or ASCT, hypocellular or marked reduction in bone marrow precursors, or history of failed stem cell collection.
Bulky areas of disease more than 10 cm in diameter.
Patients with CLL, CNS, or mantle cell lymphoma.
Hx of HIV/AIDS related lymphoma, hepatitis B or C.
Prior radioimmunotherapy or XRT to >25% of active bone marrow.
G-CSF or GM-CSF within 2 wks, pegylated G-CSF within 4 wks of treatment
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There is 1 Location for this study
Loma Linda California, , United States
Oceanside California, , United States
Fairfield Connecticut, , United States
Honolulu Hawaii, , United States
Elk Grove Village Illinois, , United States
Lafayette Indiana, , United States
Saint Louis Missouri, , United States
Charlotte North Carolina, , United States
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