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PMID: 18662969 Published · ppublish English Clinical Trial, Phase III Comparative Study Journal Article Randomized Controlled Trial

Phase III study of R-CVP compared with cyclophosphamide, vincristine, and prednisone alone in patients with previously untreated advanced follicular lymphoma.

Marcus R, Imrie K, Solal-Celigny P, Catalano JV, Dmoszynska A, Raposo JC, Offner FC, Gomez-Codina J, Belch A, Cunningham D, Wassner-Fritsch E, Stein G

Abstract

To compare the long-term outcome of patients with previously untreated follicular lymphoma (FL) needing therapy, after treatment with cyclophosphamide, vincristine and prednisone (CVP) versus CVP plus rituximab (R-CVP) and to evaluate the predictive value of known prognostic factors after treatment with R-CVP. Patients with previously untreated CD20-positive stage III/IV FL were randomly assigned to eight cycles of R-CVP (n = 159) or CVP alone (n = 162). The median follow-up period was 53 months. The primary end point-time to treatment failure (TTF), which included patients without a response after four cycles as an event-was significantly prolonged in patients receiving R-CVP versus CVP (P < .0001). Improvements in all other end points, including overall and complete response rates (P < .0001), time to progression (TTP; P < .0001), response duration (P < .0001), time to next antilymphoma treatment (P < .0001), and overall survival (OS; P = .029; 4-year OS: 83% v 77%;) were achieved with R-CVP versus CVP alone. Univariate analyses demonstrated an improvement in TTP with R-CVP versus CVP irrespective of the Follicular Lymphoma International Prognostic Index (FLIPI) subgroup, the International Prognostic Index (IPI) subgroup, baseline histology, and the presence or absence of B symptoms or bulky disease. By multivariate analysis, FLIPI retains a strong predictive power for TTP in the presence of the trial treatment effect. Analysis of all outcome measures, including OS, confirm the benefit of adding R to CVP in the front-line treatment of FL.

MeSH Terms
Antibodies, Monoclonal/administration & dosage Antibodies, Monoclonal, Murine-Derived Antineoplastic Combined Chemotherapy Protocols/therapeutic use Cyclophosphamide/administration & dosage Female Humans Lymphoma, Follicular/drug therapy,pathology Male Middle Aged Prednisone/administration & dosage Prognosis Proportional Hazards Models Rituximab Treatment Outcome Vincristine/administration & dosage
Chemicals
Antibodies, Monoclonal Antibodies, Monoclonal, Murine-Derived Rituximab Vincristine Cyclophosphamide Prednisone
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Marcus Robert
Department of Haematology, Addenbrooke's Hospital, Cambridge, UK. Robert.Marcus@kch.nhs.uk
Imrie Kevin
Solal-Celigny Philippe
Catalano John V
Dmoszynska Anna
Raposo João C
Offner Fritz C
Gomez-Codina José
Belch Andrew
Cunningham David
Wassner-Fritsch Elisabeth
Stein George
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2008-10-01
Epub
2008-00-28
Pages
4579-86
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Corrections
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