Comparison of a Standard Regimen (CHOP) with Three Intensive Chemotherapy Regimens for Advanced Non-Hodgkin's Lymphoma
Richard I. Fisher, Ellen R. Gaynor, Steve Dahlberg, Martin M. Oken, Thomas M. Grogan, Evonne M. Mize, John H. Glick, Charles A. Coltman, and Thomas P. Miller
Background CHOP is a first-generation, combination-chemotherapyregimen consisting of cyclophosphamide, doxorubicin, vincristine,and prednisone that has cured approximately 30 percent of patientswith advanced stages of intermediate-grade or high-grade non-Hodgkin'slymphoma in national cooperative-group trials. However, studiesat single institutions have suggested that 55 to 65 percentof such patients might be cured by third-generation regimenssuch as ones consisting of low-dose methotrexate with leucovorinrescue, bleomycin, doxorubicin, cyclophosphamide, vincristine,and dexamethasone (m-BACOD); prednisone, doxorubicin, cyclophosphamide,and etoposide, followed by cytarabine, bleomycin, vincristine,and methotrexate with leucovorin rescue (ProMACE-CytaBOM); andmethotrexate with leucovorin rescue, doxorubicin, cyclophosphamide,vincristine, prednisone, and bleomycin (MACOP-B).
Methods To make a valid comparison of these regimens, the SouthwestOncology Group and the Eastern Cooperative Oncology Group initiateda prospective, randomized phase III trial. The study end pointswere the response rate, time to treatment failure, overall survival,and incidence of severe or life-threatening toxicity. Dose intensitywas calculated and analyzed.
Results Of the 1138 patients registered for the trial, 899 wereeligible. Each treatment group contained at least 218 patients.Known prognostic factors were equally distributed among thegroups. There were no significant differences among the groupsin the rates of partial and complete response. At three years,44 percent of all patients were alive without disease; therewere no significant differences between the groups (41 percentin the CHOP and MACOP-B groups and 46 percent in the m-BACODand ProMACE-CytaBOM groups; P = 0.35). Overall survival at threeyears was 52 percent (50 percent in the ProMACE-CytaBOM andMACOP-B groups, 52 percent in the m-BACOD group, and 54 percentin the CHOP group; P = 0.90). There was no subgroup of patientsin which survival was improved by a third-generation regimen.Fatal toxic reactions occurred in 1 percent of the CHOP group,3 percent of the ProMACE-CytaBOM group, 5 percent of the m-BACODgroup, and 6 percent of the MACOP-B group (P = 0.09).
Conclusions CHOP remains the best available treatment for patientswith advanced-stage intermediate-grade or high-grade non-Hodgkin'slymphoma.
Source Information
From the Stritch School of Medicine, Loyola University, Maywood, Ill. (R.I.F., E.R.G.); Southwest Oncology Group Statistical Center, Seattle (S.D., E.M.M.); Virginia Piper Cancer Institute, Abbott Northwestern Hospital, Minneapolis (M.M.O.); the University of Arizona, Tucson (T.M.G., T.P.M.); the University of Pennsylvania, Philadelphia (J.H.G.); and the University of Texas Health Science Center, San Antonio (C.A.C.).
Address reprint requests to the Southwest Oncology Group (SWOG-8516), Operations Office, 5430 Fredericksburg Rd., Suite No. 618, San Antonio, TX 78229-6197.
Observational Studies and Randomized Trials
Kunz R., Khan K. S., Neumayer H.-H., Sacks H. S., Liu P.-Y., Anderson G., Crowley J. J., Friedman H. S., Smith R. P., Meier P., Benson K., Hartz A. J., Concato J., Shah N., Horwitz R. I.
Extract |
Full Text
N Engl J Med 2000;
343:1194-1197, Oct 19, 2000.
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