Standard chemotherapy with or without high-dose chemotherapy for aggressive non-Hodgkin's lymphoma: Randomized phase III EORTC study

被引:104
作者
Kluin-Nelemans, HC
Zagonel, V
Anastasopoulou, A
Bron, D
Roozendaal, KJ
Noordijk, EM
Musson, H
Teodorovic, I
Maes, B
Carbone, A
Carde, P
Thomas, J
机构
[1] Leiden Univ, Med Ctr, Dept Hematol, NL-2300 RA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Radiotherapy, NL-2300 RA Leiden, Netherlands
[3] Natl Canc Inst, Dept Pathol, Aviano, Italy
[4] Natl Canc Inst, Dept Oncol, Aviano, Italy
[5] EORTC, Data Ctr, Brussels, Belgium
[6] Onze Lieve Vrouwen Gasthuis, Amsterdam, Netherlands
[7] Univ Hosp, Dept Pathol, Louvain, Belgium
[8] Univ Hosp, Dept Oncol, Louvain, Belgium
[9] Inst Gustave Roussy, EORTC Lymphoma Grp, Villejuif, France
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2001年 / 93卷 / 01期
关键词
D O I
10.1093/jnci/93.1.22
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The long-term outcome for patients with aggressive non-Hodgkin's lymphoma (NHL) is poor. Consequently; the European Organization for Research and Treatment of Cancer Lymphoma Group designed a prospective randomized trial to investigate whether high-dose chemotherapy plus autologous bone marrow transplantation (ABMT) after standard combination chemotherapy improves long-term survival. Methods: Patients aged 15-65 years with aggressive NHL received three cycles of CHVmP/BV polychemotherapy (i.e., a combination of cyclophosphamide, doxorubicin, teniposide, and prednisone, with bleomycin and vincristine added at mid-cycle). After these three cycles, patients With a complete or partial remission and at that time no lymphoma involvement in the bone marrow were randomly assigned to the ABMT arm (a further three cycles of CHVmP/BV followed by BEAC [i.e., a combination of carmustine, etoposide, cytarabine, and cyclophosphamide] chemotherapy and ABMT) or to the control arm (five more cycles: of CHVVmP/BV). All statistical tests are two-sided. Results: From December 1990 through October 1998, 311 patients (median age = 44 years) were registered and received the first-three cycles of CHVmP/BV, and 194 patients were randomly assigned to the treatment arms. Approximately 70% (140 patients) of these patients were of low or low-intermediate International Prognostic Index (IPI) risk. After a median follow-up of 53 months, an intention-to-treat analysis' Showed a time to disease progression and overall survival: at 5 years of 61% (95% confidence interval [CI] = 51% to 72%) and 68% (95% CI = 57% to 79%), respectively, for the ABMT arm and 56% (95% CI = 45% to 67%) and 77% (95% CI = 67% to 86%), respectively, for the control arm. Differences between arms were not statistically significant. A subset analysis on IPI risk groups, although too small for reliable statistical analysis, yielded similar results. Conclusions: Standard combination therapies remain the best choice for most patients with aggressive NHL, We recommend that patients,vith IPI low or low-intermediate risk not be subjected to high-dose chemotherapy and ABMT as a first-line therapy.
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页码:22 / 30
页数:9
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