Combination Chemo, Rituximab, and Bevacizumab in Older Patients With Stage II-IV Diffuse Large B-Cell Lymphoma
Part of paid clinical trials in Portland, Oregon.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00121199
- Phase
- PHASE2
- Status
- Completed
Conditions
- Contiguous Stage II Adult Diffuse Large Cell Lymphoma
- Noncontiguous Stage II Adult Diffuse Large Cell Lymphoma
- Stage III Adult Diffuse Large Cell Lymphoma
- Stage IV Adult Diffuse Large Cell Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- rituximab — BIOLOGICALGiven IV
- bevacizumab — BIOLOGICALGiven IV
- cyclophosphamide — DRUGGiven IV
- doxorubicin hydrochloride — DRUGGiven IV
- vincristine sulfate — DRUGGiven IV
- prednisone — DRUGGiven PO
- laboratory biomarker analysis — OTHERCorrelative studies
Study Details
This phase II trial is studying how well giving combination chemotherapy together with rituximab and bevacizumab works in treating older patients with stage II, stage III, or stage IV diffuse large B-cell lymphoma. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more cancer cells. Monoclonal antibodies, such as rituximab and bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Bevacizumab may also stop the growth of cancer cells by blocking blood flow to the cancer. Giving combination chemotherapy together with monoclonal antibodies may kill more cancer cells.
Key Dates
- Start date
- Jun 30, 2005
- Status verified
- Dec 2012
- Primary completion
- Dec 31, 2010
- Completion
- Dec 31, 2010
Study Design
- Enrollment
- 73 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (CHOP, rituximab, bevacizumab)Patients receive rituximab IV, bevacizumab IV over 30-90 minutes, cyclophosphamide IV over 15 minutes, doxorubicin IV, and vincristine IV on day 1. Patients also receive oral prednisone on days 1-5. Treatment repeats every 21 days for 8 courses in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Progression-free Survival at 1 Year [ Time Frame: 0-1 year ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| SWOG | Portland | Oregon | 97239 | - |