MabThera (Rituximab) Plus Cyclophosphamide, Vincristine and Prednisone (CVP) Chemotherapy Improves Survival in Previously Untreated Patients with Advanced Follicular Non-Hodgkin’s Lymphoma (NHL).

Author:

Marcus Robert E.1,Solal-Celigny Philippe2,Imrie Kevin3,Catalano John V.4,Dmoszynska Anna5,Raposo João C.6,Offner Fritz C.7,Gomez-Codina José8

Affiliation:

1. Department of Hematology, Addenbrooke’s Hospital, Cambridge, United Kingdom

2. Clinique Victor Hugo, Le Mans, France

3. Toronto-Sunnybrook Regional Cancer Centre, Toronto, ON, Canada

4. Department of Haematology, Monash Medical Centre, Clayton, Victoria, Australia

5. Haematology Department, Medical University of Lublin, Lublin, Poland

6. Servico de Hematologia, Hospital Santa Maria, Lisboa, Portugal

7. Dienst Hematologie, Universitair Ziekenhuis, Gent, Belgium

8. Servicio de Oncologá Médica, Hospital La Fe de Valencia, Valencia, Spain

Abstract

Abstract Design/methods: Rituximab added to 8 cycles of CVP (R-CVP) chemotherapy improves time to progression and duration of response in previously untreated patients with stage III/IV CD20 positive follicular NHL compared with CVP alone (Marcus et al Blood2005;105:1417–23). A protocol pre-planned analysis of this study with a median follow-up of 53 months has now been performed. Results: A total of 321 patients (median age 53 years) were recruited. Eighty-three percent of patients in both arms had intermediate to high-risk disease according to the Follicular Lymphoma International Prognostic Index (FLIPI, score 2–5). Median time to progression or death (TTP) in the R-CVP arm was 34 months compared with 15 months in the CVP arm, p<0.0001 (log rank). This increase in TTP was observed in all FLIPI groups with a risk ratio of 0.40 (95% confidence interval 0.27 to 0.60) for good intermediate risk patients and 0.51 (95% confidence interval 0.34 to 0.76) for poor risk patients; overall the risk ratio was 0.44 (95% confidence interval 0.32 to 0.57). In patients achieving a complete response (CR) or CR unconfirmed (CRu), disease-free survival (DFS) was significantly prolonged (p=0.0001, log rank); the estimated 4-years’ DFS rate was 54% for patients receiving R-CVP compared with 17% for CVP. Nineteen percent (31/162) of patients in the R-CVP group have now died compared with 29% (46/159 patients) in the CVP group. Patients receiving R-CVP had a significant improvement in overall survival compared with CVP (p=0.03, log rank; hazard ratio 0.60 [95% confidence interval 0.38 to 0.96]). Conclusion: When added to first-line chemotherapy in patients with follicular NHL, rituximab not only improves TTP and DFS, but also has a favorable effect on overall survival.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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