ABVD Compared With BEACOPP Compared With CEC for the Initial Treatment of Patients With Advanced Hodgkin's Lymphoma: Results From the HD2000 Gruppo Italiano per lo Studio dei Linfomi Trial

被引:229
作者
Federico, Massimo [1 ]
Luminari, Stefano
Iannitto, Emilio
Polimeno, Giuseppe
Marcheselli, Luigi
Montanini, Antonella
La Sala, Antonio
Merli, Francesco
Stelitano, Caterina
Pozzi, Samantha
Scalone, Renato
Di Renzo, Nicola
Musto, Pellegrino
Baldini, Luca
Cervetti, Giulia
Angrilli, Francesco
Mazza, Patrizio
Brugiatelli, Maura
Gobbi, Paolo G.
机构
[1] Univ Modena & Reggio Emilia, Ctr Oncol Modenese, Dipartimento Oncol & Ematol, I-41100 Modena, Italy
关键词
LIMITED RADIOTHERAPY; COMBINATION CHEMOTHERAPY; PROGNOSTIC SCORE; STANFORD-V; DISEASE; HYBRID; STAGE; MOPP; VINBLASTINE; MOPPEBVCAD;
D O I
10.1200/JCO.2008.17.0910
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose To compare doxorubicin, bleomycin, vinblastine, dacarbazine (ABVD) versus bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP) versus cyclophosphamide, lomustine, vindesine, melphalan, prednisone, epidoxirubicin, vincristine, procarbazine, vinblastine, and bleomycin (COPPEBVCAD; CEC) for advanced Hodgkin's lymphoma (HL). Patients and Methods Three hundred seven patients with advanced HL (stage IIB, III, and IV) were randomly assigned to receive six courses of ABVD, four escalated plus two standard courses of BEACOPP, or six courses of CEC, plus a limited radiation therapy program. Results After a median follow-up of 41 months, BEACOPP resulted in a superior progression-free survival (PFS), with a significant reduction in risk of progression (hazard ratio [HR] = 0.50) compared with ABVD. No differences between BEACOPP and CEC, or CEC and ABVD were observed. The 5-year PFS was 68% (95% Cl, 56% to 78%), 81% (95% Cl, 70% to 89%), and 78% (95% Cl, 68% to 86%), for ABVD, BEACOPP, and CEC, respectively (BEACOPP v ABVD, P = .038; CEC v ABVD and BEACOPP v CEC, P = not significant [NS]). The 5-year overall survival was 84% (95% Cl, 69% to 92%), 92% (95% Cl, 84% to 96%), and 91% (95% Cl, 81% to 96%) for ABVD, BEACOPP, and CEC, respectively (P = NS). BEACOPP and CEC resulted in higher rates of grade 3-4 neutropenia than ABVD (P = .016); BEACOPP was associated with higher rates of severe infections than ABVD and CEC (P = .003). Conclusion As adopted in this study BEACOPP is associated with a significantly improved PFS compared with ABVD, with a predictable higher acute toxicity.
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收藏
页码:805 / 811
页数:7
相关论文
共 32 条
[1]
The revised CONSORT statement for reporting randomized trials: Explanation and elaboration [J].
Altman, DG ;
Schulz, KF ;
Moher, D ;
Egger, M ;
Davidoff, F ;
Elbourne, D ;
Gotzsche, PC ;
Lang, T .
ANNALS OF INTERNAL MEDICINE, 2001, 134 (08) :663-694
[2]
ARMITAGE P, 1987, STATISTICAL METHODS, P125
[3]
BONADONNA G, 1975, CANCER, V36, P252, DOI 10.1002/1097-0142(197507)36:1<252::AID-CNCR2820360128>3.0.CO
[4]
2-7
[5]
CHEMOTHERAPY OF ADVANCED HODGKINS-DISEASE WITH MOPP, ABVD, OR MOPP ALTERNATING WITH ABVD [J].
CANELLOS, GP ;
ANDERSON, JR ;
PROPERT, KJ ;
NISSEN, N ;
COOPER, MR ;
HENDERSON, ES ;
GREEN, MR ;
GOTTLIEB, A ;
PETERSON, BA .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (21) :1478-1484
[6]
Primary systemic treatment of advanced Hodgkin's disease with EVA (etoposide, vinblastine, doxorubicin): 10-year follow-up [J].
Canellos, GP ;
Gollub, J ;
Neuberg, D ;
Mauch, P ;
Shulman, LN .
ANNALS OF ONCOLOGY, 2003, 14 (02) :268-272
[7]
Connors Joseph M, 2005, Hematology Am Soc Hematol Educ Program, P239, DOI 10.1182/asheducation-2005.1.239
[8]
COX DR, 1972, J R STAT SOC B, V34, P187
[9]
DEVITA VT, 1987, CANCER RES, V47, P5810
[10]
BEACOPP, a new dose-escalated and accelerated regimen, is at least as effective as COPP/ABVD in patients with advanced-stage Hodgkin's lymphoma: Interim report from a trial of the German Hodgkin's Lymphoma Study Group [J].
Diehl, V ;
Franklin, J ;
Hasenclever, D ;
Tesch, H ;
Pfreundschuh, M ;
Lathan, B ;
Paulus, U ;
Sieber, M ;
Rueffer, JU ;
Sextro, M ;
Engert, A ;
Wolf, J ;
Hermann, R ;
Holmer, L ;
Stappert-Jahn, U ;
Winnerlein-Trump, E ;
Wulf, G ;
Krause, S ;
Glunz, A ;
von Kalle, K ;
Bischoff, H ;
Haedicke, C ;
Duehmke, E ;
Georgii, A ;
Loeffler, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3810-3821