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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
138
375 mg/m², D1, 4 cycles
75 mg/m², D1, 4 cycles
1200 mg/m², D1, 4 cycles
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
event free survival
percentage of patients alive with no event
Time frame: 8 years (end of study)
complete response rate
percentage of patients with complete response
Time frame: 8 years (end of study)
progression rate
percentage of patients with progression
Time frame: 8 years (end of study)
relapse rate
percentage of patients with relapse
Time frame: 8 years (end of study)
disease-free survival for complete responders
percentage of patients with complete response who remain disease-free
Time frame: 8 years (end of study)
overall survival
percentage of patients alive
Time frame: 8 years (end of study)
neuromeningeal relapse rate
percentage of patients with neuromeningeal relapse
Time frame: 8 years (end of study)
number of SAE
Time frame: 8 years (end of study)
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2 mg/m², D1, D5, 4 cycles
10 mg, D1, D5, 4 cycles
60 mg, D1-D5, 4 cycles
40 mg, D1-D5, 4 cycles
50 mg/m², D1, 4 cycles
750 mg/m², D1, 4 cycles
1.4 mg/m², D1, 4 cycles
Centre Hospitalier Robert Debré
Reims, France
Centre Henri Becquerel
Rouen, France
Institut Gustave Roussy
Villejuif, France
Schweirische Arbeitsgruppe fur klinische Krebsforschung
Lausanne, Switzerland