R-CHOP-14 Versus R-CHOP-21 and Darbepoetin Alpha in Patients Aged 60-80 Years With Diffuse Large B-cell Lymphoma
Diffuse Large Cell Lymphoma
About this trial
This is an interventional treatment trial for Diffuse Large Cell Lymphoma focused on measuring lymphoma, diffuse large B-cell, rituximab, chemotherapy, erythropoetin, darbepoetin alfa
Eligibility Criteria
Inclusion Criteria: Patients with histologically proven CD20+ diffuse large B cell lymphoma (WHO Classification). Aged 66 to 80 years old. Patients not previously treated. Ann Arbor stage II, III, IV. ECOG performance status 0 to 2. Age-adjusted IPI equal to 1, 2, or 3. With a minimum life expectancy of 3 months. Negative HIV, HBV and HCV serologies test < 4 weeks (except after vaccination for HBV). Having signed a written informed consent. Exclusion Criteria: Any other histological type of lymphoma. Any history of treated or non-treated indolent lymphoma. However, patients not previously diagnosed and having a diffuse large B-cell lymphoma with some small cell infiltration in bone marrow or lymph node may be included. Central nervous system or meningeal involvement by lymphoma. Contra-indication to any drug contained in the chemotherapy regimens. Any serious co-morbid active disease (according to the investigator's decision). Poor renal function (creatinin level > 150 micromol/l), poor hepatic function (total bilirubin level > 30mmol/l, transaminases > 2.5 maximum normal level) unless these abnormalities are related to the lymphoma. Poor bone marrow reserve as defined by neutrophils < 1.5 G/l or platelets < 100 G/l, unless related to bone marrow infiltration. Any history of cancer during the last 5 years with the exception of non-melanoma skin tumors or stage 0 (in situ) cervical carcinoma. Uncontrolled hypertension. Known hypersensitivity to erythropoietin. Myocardial infarction during last 3 month, or unstable coronary disease, or uncontrolled cardiac insufficiency. Venous thrombosis or pulmonary embolism during last 3 months. Treatment with any investigational drug within 30 days before planned first cycle of chemotherapy and during the study. Pregnant or lactating women. Adult patient under tutelage.
Sites / Locations
- Université de Gent
- Groupe d'Etude des Lymphomes de l'adulte
- Polyclinique Bordeaux Nord
- Hôpital Henri Mondor
- Hématologie CHU de Lille
- Centre Léon Bérard
- Hôpital Saint Louis
- Hématologie Adultes - Hôpital Necker
- Service d'Hématologie - Centre Hospitalier Lyon-Sud
- Centre Hospitalier Robert Debré
- Centre Henri Becquerel
- Hématologie CHU Purpan
- Institut Gustave Roussy
- Schweirische Arbeitsgruppe fur klinische Krebsforschung
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Experimental
Experimental
Experimental
R-CHOP21
R-CHOP21, Darbepoetin alfa
R-CHOP14
R-CHOP14, Darbepoetin alfa
8 cycles of R-CHOP21
8 cycles of R-CHOP21 + prophylactic darbepoetin alfa
8 cycles of R-CHOP14
8 cycles of R-CHOP14 + prophylactic darbepoetin alfa