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Randomized Study of ACVBP Plus Rituximab Versus CHOP Plus Rituximab in Non Previously Treated Patients Aged From 60 to 65 Years With Diffuse Large B-Cell Lymphoma
The primary objective of this study is to evaluate the efficacy of doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone (ACVBP) plus rituximab in comparison to cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) plus rituximab in patients aged from 60 to 65 years with non-previously treated diffuse large B-cell lymphoma as measured by the event-free survival. The goal is to obtain a 10% increase of event-free survival at 3 years.
In Europe, 50% or more of new non-Hodgkin lymphoma cases occur in patients older than 60 years. More than 30% are diffuse large B-cell lymphomas (DLCL). The CHOP chemotherapy (cyclophosphamide, doxorubicin, vincristine, prednisone) was considered as the standard treatment in this population. Nevertheless, this treatment is associated with some toxic events in elderly patients and it did does not succeed to increase the 3-year survival rate above 40%. Two trials in patients above 60 years with DLCL cases were conducted by the GELA in the aim to improve the results of CHOP. Protocol LNH 93-5 : The primary objective of this study was to compare CHOP to ACVBP in patients aged from 61 to 69 years with aggressive lymphoma and at least one adverse prognostic factor according to the International Prognostic Index. Unlike the CHOP regimen, the ACVBP regimen includes a more intensive induction followed by a sequential consolidation with drugs different from those used during the induction phase, and includes a prevention of neuromeningeal relapses. Out of 708 patients included in this study, the results have shown that: * Complete response rate was the same in the two arms. * Event free survival was significantly better in the ACVBP arm than the CHOP arm ( 5-year survival rate : 39% versus 29%, p=0.005). * Overall survival was significantly better in the ACVBP arm than in the CHOP arm (the 5-year survival rate : 46% versus 38%, p=0.036). * The ACVBP regimen was more toxic than the CHOP regimen, particularly in elderly patients (\> 65 years) and in patients with a low performance status. * Prevention of neuromeningeal relapses was necessary for these patients. Protocol LNH 98-5, the objective of this study was to compare the association CHOP + rituximab (R-CHOP) to the CHOP regimen alone in elderly patients with non previously treated diffuse large B-cell lymphoma. Long-term results based on data from 399 patients, with a median follow-up of 5 years were as follows : * Complete response rate was better in the R-CHOP arm than in the CHOP arm (76% versus 61%, p\<0.005). * Significant prolongation of event-free survival (p\<0.0002) and overall survival (p\<0.0073) in the R-CHOP arm. * No significant difference between the two arms in terms of toxicity. R-CHOP is now considered worldwide as the standard combination for these patients. These conclusions invited us to propose a randomized trial comparing ACVBP + rituximab to CHOP + rituximab. The study population is limited to patients aged from 60 to 65 years.
Age
60 - 65 years
Sex
ALL
Healthy Volunteers
No
Groupe d'Etude des Lymphomes de l'adulte
Yvoir, Belgium
Hôpital Henri Mondor
Créteil, France
Hôpital Saint Louis
Paris, France
Service d'Hématologie - Centre Hospitalier Lyon-Sud
Pierre-Bénite, France
Centre Hospitalier Robert Debré
Reims, France
Centre Henri Becquerel
Rouen, France
Institut Gustave Roussy
Villejuif, France
Schweirische Arbeitsgruppe fur klinische Krebsforschung
Lausanne, Switzerland
Start Date
October 16, 2001
Primary Completion Date
April 27, 2010
Completion Date
April 27, 2010
Last Updated
August 23, 2018
138
ACTUAL participants
Rituximab
DRUG
Doxorubicin
DRUG
Cyclophosphamide
DRUG
Vindesine
DRUG
Bleomycin
DRUG
Prednisone
DRUG
Prednisone
DRUG
Doxorubicin
DRUG
Cyclophosphamide
DRUG
Vincristine
DRUG
Lead Sponsor
Lymphoma Study Association
Collaborators
NCT00498914
NCT00511043
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT00379574