
pmid: 10707786
Between 1987 and 1991, the British National Lymphoma Investigation randomized 459 patients with non-Hodgkin's lymphoma with a large-cell component to either CHOP or the PACEBOM regimen.Four hundred fifty-nine eligible patients were included in this trial, four hundred one with diffuse large-cell lymphoma and fifty-eight with diffuse mixed-cell lymphoma according to the Working Formulation. Two hundred twenty-six patients were randomized to receive CHOP and two hundred thirty-three to receive PACEBOM. The two arms of the trial were well balanced for all potential prognostic factors.The complete remission rate with PACEBOM was 64% and with CHOP 57% (NS). At eight years, the actuarial cause specific survival (CSS) in the PACEBOM arm is 59% compared to 49% in the CHOP arm (P = 0.09). Patients < 50 years of age fared significantly better in the PACEBOM arm both for CSS and overall survival (P = 0.002) and the CSS was also significantly improved in stage IV disease (P = 0.02).The mature data from this trial suggest that an etoposide-containing multi-agent weekly regimen can be superior to CHOP.
Adult, Male, Chi-Square Distribution, Adolescent, Dose-Response Relationship, Drug, Lymphoma, Non-Hodgkin, Middle Aged, Drug Administration Schedule, Bleomycin, Methotrexate, Doxorubicin, Antineoplastic Combined Chemotherapy Protocols, Humans, Female, Neoplasm Invasiveness, Lymphoma, Large B-Cell, Diffuse, Cyclophosphamide, Aged, Etoposide, Follow-Up Studies
Adult, Male, Chi-Square Distribution, Adolescent, Dose-Response Relationship, Drug, Lymphoma, Non-Hodgkin, Middle Aged, Drug Administration Schedule, Bleomycin, Methotrexate, Doxorubicin, Antineoplastic Combined Chemotherapy Protocols, Humans, Female, Neoplasm Invasiveness, Lymphoma, Large B-Cell, Diffuse, Cyclophosphamide, Aged, Etoposide, Follow-Up Studies
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