Shortened first-line high-dose chemotherapy for patients with poor-prognosis aggressive lymphoma

被引:154
作者
Gisselbrecht, C
Lepage, E
Molina, T
Quesnel, B
Fillet, G
Lederlin, P
Coiffier, B
Tilly, H
Gabarre, J
Guilmin, F
Hermine, O
Reyes, F
机构
[1] Hop St Louis, Inst Hematol, GELA, F-75475 Paris 10, France
[2] Hop Hotel Dieu, Serv Anat Pathol, Paris, France
[3] Hop La Pitie Salpetriere, Hematol Serv, Paris, France
[4] Hop Necker Enfants Malad, Hematol Serv, Paris, France
[5] Hop Henri Mondor, Dept Informat Hosp, F-94010 Creteil, France
[6] Hop Henri Mondor, Hematol Serv, F-94010 Creteil, France
[7] CHU Lille, F-59037 Lille, France
[8] CHU Brabois, Serv Hematol & Med Interne, Vandoeuvre Les Nancy, France
[9] Ctr Hosp Lyon Sud, F-69310 Pierre Benite, France
[10] Ctr Henri Becquerel, F-76038 Rouen, France
[11] Hop Beaujon, Hematol Serv, Clichy, France
[12] CHu Liege, Domaine Univ Sart Tilman, Liege, Belgium
关键词
D O I
10.1200/JCO.2002.02.125
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Randomized trial LNH93-3 was conducted on patients who had poor-prognosis aggressive lymphoma and were younger than 60 years with two to three factors of the age-adjusted International Prognostic Index to evaluate the benefit of early high-dose therapy (HDT) with autologous stem-cell transplantation (ASCT). Patients and Methods: Patients were randomized between doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone (ACVBP) chemotherapy followed by sequential consolidation and an experimental shortened treatment consisting of three cycles with escalated doses of cyclophosphamide, epirubicin, vindesine, bleomycin, and prednisone and collection of peripheral-blood stem cells. On day 60, HDT was administered with 1,3-bis(2-chloroethyl)-1-nitrosourea, etoposide, cytarabine, and melphalan followed by ASCT. Results: Eligible patients (n = 370) with aggressive lymphoma were analyzed. For ACVBP (181 patients) and HDT (189 patients), respective complete remission rates were 64% and 63%. With a median follow-up of 60 months, 5-year overall survival and event-free survival for ACVBP and HDT were 60% +/- 8% and 46% +/- 8% (P = .007) and 52 +/- 8% and 39 8% (P = .01), respectively. Survival was independently affected by age greater than 40 years (P = .0003), T-cell phenotype (P = .009), bone marrow involvement (P = .003), and HDT treatment group (P = .04). Conclusion: Early HDT with ASCT in high-risk patients was inferior to the ACVBP chemotherapy regimen. These results indicate that the received dose-intensity before HDT was too low when compared with ACVBP and HDT and was given too early. (C) 2002 by American Society of Clinical Oncology.
引用
收藏
页码:2472 / 2479
页数:8
相关论文
共 38 条
[1]
Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[2]
LNH-84 REGIMEN - A MULTICENTER STUDY OF INTENSIVE CHEMOTHERAPY IN 737 PATIENTS WITH AGGRESSIVE MALIGNANT-LYMPHOMA [J].
COIFFIER, B ;
GISSELBRECHT, C ;
HERBRECHT, R ;
TILLY, H ;
BOSLY, A ;
BROUSSE, N .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (08) :1018-1026
[3]
CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. [J].
Coiffier, B ;
Lepage, E ;
Brière, J ;
Herbrecht, R ;
Tilly, H ;
Bouabdallah, R ;
Morel, P ;
Van den Neste, E ;
Salles, G ;
Gaulard, P ;
Reyes, F ;
Gisselbrecht, C .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :235-242
[4]
Clinical outcome after autologous transplantation in non-Hodgkin's lymphoma patients with high international prognostic index (IPI) [J].
Cortelazzo, S ;
Rossi, A ;
Bellavita, P ;
Oldani, E ;
Viero, P ;
Buelli, M ;
Rambaldi, A ;
Barbui, T .
ANNALS OF ONCOLOGY, 1999, 10 (04) :427-432
[5]
COX DR, 1972, J R STAT SOC B, V34, P187
[6]
COMPARISON OF A STANDARD REGIMEN (CHOP) WITH 3 INTENSIVE CHEMOTHERAPY REGIMENS FOR ADVANCED NON-HODGKINS-LYMPHOMA [J].
FISHER, RI ;
GAYNOR, ER ;
DAHLBERG, S ;
OKEN, MM ;
GROGAN, TM ;
MIZE, EM ;
GLICK, JH ;
COLTMAN, CA ;
MILLER, TP .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (14) :1002-1006
[7]
AUTOLOGOUS BONE-MARROW TRANSPLANTATION IN POOR-PROGNOSIS INTERMEDIATE-GRADE AND HIGH-GRADE B-CELL NON-HODGKINS-LYMPHOMA IN 1ST REMISSION - A PILOT-STUDY [J].
FREEDMAN, AS ;
TAKVORIAN, T ;
NEUBERG, D ;
MAUCH, P ;
RABINOWE, SN ;
ANDERSON, KC ;
SOIFFER, RJ ;
SPECTOR, N ;
GROSSBARD, M ;
ROBERTSON, MJ ;
BLAKE, K ;
CORAL, F ;
CANELLOS, GP ;
RITZ, J ;
NADLER, LM .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (05) :931-936
[8]
High-dose chemotherapy and autologous bone marrow transplantation compared with MACOP-B in aggressive B-cell lymphoma [J].
Gianni, AM ;
Bregni, M ;
Siena, S ;
Brambilla, C ;
DiNicola, M ;
Lombardi, F ;
Gandola, L ;
Tarella, C ;
Pileri, A ;
Ravagnani, F ;
Valagussa, P ;
Bonadonna, G ;
Stern, AC ;
Magni, M ;
Caracciolo, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (18) :1290-1297
[9]
Gisselbrecht C, 1998, BLOOD, V92, P76
[10]
Placebo-controlled phase III study of lenograstim (glycosylated recombinant human granulocyte colony-stimulating factor) in aggressive non-Hodgkin's lymphoma: Factors influencing chemotherapy administration [J].
Gisselbrecht, C ;
Haioun, C ;
Lepage, E ;
Bastion, Y ;
Tilly, H ;
Bosly, A ;
Dupriez, B ;
Marit, G ;
Herbrecht, R ;
Deconinck, E ;
Marolleau, JP ;
Yver, A ;
DabouzHarrouche, F ;
Coiffier, B ;
Reyes, F .
LEUKEMIA & LYMPHOMA, 1997, 25 (3-4) :289-300