International Phase II Study Evaluating the Association of CHOP-rituximab With Consolidation by Early Ibritumomab Tiuxetan-Y90 in Patients Aged 65 to 80 Years With CD20+ Large Cell Malignant Lymphoma and no Prior Therapy
Overview
- Phase
- Phase 2
- Intervention
- rituximab
- Conditions
- Lymphoma
- Sponsor
- Centre Antoine Lacassagne
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Event-free survival
- Status
- Completed
- Last Updated
- 7 months ago
Overview
Brief Summary
RATIONALE: Drugs used in chemotherapy, such as doxorubicin, vincristine, and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Steroid therapy, such as prednisone, may be effective in treating cancer and blocking the body's immune response. Monoclonal antibodies, such as rituximab and yttrium Y 90 ibritumomab tiuxetan, 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. Giving chemotherapy together with prednisone and monoclonal antibody therapy may kill more cancer cells.
PURPOSE: This phase II trial is studying how well giving doxorubicin together with vincristine, cyclophosphamide, prednisone, and rituximab followed by rituximab and yttrium Y 90 ibritumomab tiuxetan works in treating patients with newly diagnosed large B-cell lymphoma.
Detailed Description
OBJECTIVES: Primary * Determine event-free survival of patients with large B-cell lymphoma treated with CHOP-R followed by consolidation therapy. Secondary * Determine overall survival. * Evaluate relapse-free survival for patients achieving complete or partial response. * Determine the rate of disease progression. * Determine response rate at the end of study therapy. * Assess the toxicities of this regimen. OUTLINE: This is a multicenter study. * Induction therapy: Patients receive the CHOP-R regimen comprising doxorubicin hydrochloride IV, vincristine IV, cyclophosphamide IV, and rituximab IV on day 1 and prednisone IV on days 1-5. Treatment repeats every 2 weeks for 2 courses. Patients who achieve complete or partial response, as assessed by PET/CT scan, receive a third course of induction therapy. * Consolidation therapy: Patients receive rituximab IV on days -8 to 0 and yttrium Y 90 ibritumomab tiuxetan IV on day 0.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
R-CHOP14 chemotherapy
Intervention: rituximab
R-CHOP14 chemotherapy
Intervention: cyclophosphamide
R-CHOP14 chemotherapy
Intervention: doxorubicin hydrochloride
R-CHOP14 chemotherapy
Intervention: prednisone
R-CHOP14 chemotherapy
Intervention: vincristine sulfate
R-CHOP14 chemotherapy
Intervention: yttrium Y 90 ibritumomab tiuxetan
Outcomes
Primary Outcomes
Event-free survival
Time Frame: 1 year
Secondary Outcomes
- Overall survival(up to one year)
- Relapse-free survival in responding patients(up to one year)
- Rate of disease progression(up to 2 years)
- Response rate(up to six months)
- Toxicities(up to 2 years)