Dose-intense chemotherapy every 2 weeks with dose-intense cyclophosphamide, doxorubicin, vincristine, and prednisone may improve survival in intermediate- and high-grade lymphoma: A phase II study of the Southwest Oncology Group (SWOG 9349)

被引:67
作者
Blayney, DW
LeBlanc, ML
Grogan, T
Gaynor, ER
Chapman, RA
Spiridonidis, CH
Taylor, SA
Bearman, SI
Miller, TP
Fisher, RI
机构
[1] Wilshire Oncol Med Grp Inc, Pasadena, CA USA
[2] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[3] Univ Arizona, Ctr Canc, Tucson, AZ USA
[4] Loyola Univ, Stritch Sch Med, Maywood, IL 60153 USA
[5] Henry Ford Hosp, Detroit, MI 48202 USA
[6] Columbus Community Clin Oncol Program, Columbus, OH USA
[7] Univ Kansas, Med Ctr, Kansas City, MO USA
[8] Univ Colorado, Sch Med, Denver, CO USA
[9] Univ Rochester, Sch Med, Rochester, NY USA
关键词
D O I
10.1200/JCO.2003.06.137
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To test the hypothesis that therapy of intermediate- and high-grade (excluding Burkitt lymphoblastic) lymphoma with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) could be safely dose-intensified with routine filgrastim support. Patients and Methods: Eligible patients were those who were previously untreated and who had either bulky stage II, or stage III or IV lymphoma with working formulation histology D, E, F, G, H, or J; performance status :5 2; and acceptable end organ function. No upper age limit was specified. Therapy was dose-intensified CHOP (CHOP-DI) with filgrastim support. Each course was repeated every 14 days for six planned courses. Results: Eighty-eight eligible patients were treated with CHOP-DI and had a median follow-up of 5.1 years on this phase II study, designated Southwest Oncology Group (SWOG) 9349. The progression-free survival was 51% at 2 years and 41% at 5 years. The overall survival was 60% at 5 years. Three fatal treatment-related events occurred. One patient with myelodysplastic syndrome was reported. Conclusion: Treatment with CHOP-DI can be safely administered in the cooperative group setting and results in improved survival. Estimated overall survival at 5 years was 14% better than that of patients treated with standard-dose CHOP in an earlier SWOG study, although progression-free survival of 60% at 2 years-the prespecified end point-was not achieved. CHOP-DI, given every 2 weeks at escalated doses, is a strategy that should be tested in a future randomized clinical trial in lymphoma. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:2466 / 2473
页数:8
相关论文
共 35 条
[31]   HIGH-DOSE CHOP AS INITIAL THERAPY FOR PATIENTS WITH POOR-PROGNOSIS AGGRESSIVE NON-HODGKINS-LYMPHOMA - A DOSE-FINDING PILOT-STUDY [J].
SHIPP, MA ;
NEUBERG, D ;
JANICEK, M ;
CANELLOS, GP ;
SHULMAN, LN .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (12) :2916-2923
[32]   International consensus conference on high-dose therapy with hematopoietic stem cell transplantation in aggressive non-hodgkin's lymphomas: Report of the jury [J].
Shipp, MA ;
Abeloff, MD ;
Antman, KH ;
Carroll, G ;
Hagenbeek, A ;
Loeffler, M ;
Montserrat, E ;
Radford, JA ;
Salles, G ;
Schmitz, N ;
Symann, M ;
Armitage, JO ;
Philip, T ;
Coiffier, B .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (01) :423-429
[33]   A PREDICTIVE MODEL FOR AGGRESSIVE NON-HODGKINS-LYMPHOMA [J].
SHIPP, MA ;
HARRINGTON, DP ;
ANDERSON, JR ;
ARMITAGE, JO ;
BONADONNA, G ;
BRITTINGER, G ;
CABANILLAS, F ;
CANELLOS, GP ;
COIFFIER, B ;
CONNORS, JM ;
COWAN, RA ;
CROWTHER, D ;
DAHLBERG, S ;
ENGELHARD, M ;
FISHER, RI ;
GISSELBRECHT, C ;
HORNING, SJ ;
LEPAGE, E ;
LISTER, TA ;
MEERWALDT, JH ;
MONTSERRAT, E ;
NISSEN, NI ;
OKEN, MM ;
PETERSON, BA ;
TONDINI, C ;
VELASQUEZ, WA ;
YEAP, BY .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (14) :987-994
[34]   Phase II study of rituximab in combination with CHOP chemotherapy in patients with previously untreated, aggressive non-Hodgkin's lymphoma [J].
Vose, JM ;
Link, BK ;
Grossbard, ML ;
Czuczman, M ;
Grillo-Lopez, A ;
Gilman, P ;
Lowe, A ;
Kunkel, LA ;
Fisher, RI .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (02) :389-397
[35]   Dose-adjusted EPOCH chemotherapy for untreated large B-cell lymphomas: a pharmacodynamic approach with high efficacy [J].
Wilson, WH ;
Grossbard, ML ;
Pittaluga, S ;
Cole, D ;
Pearson, D ;
Drbohlav, N ;
Steinberg, SM ;
Little, RF ;
Janik, J ;
Gutierrez, M ;
Raffeld, M ;
Staudt, L ;
Cheson, BD ;
Longo, DL ;
Harris, N ;
Jaffe, ES ;
Chabner, BA ;
Wittes, R ;
Balis, F .
BLOOD, 2002, 99 (08) :2685-2693