CHOP versus MACOP-B in aggressive lymphoma -: a Nordic Lymphoma Group randomised trial

被引:47
作者
Jerkeman, M [1 ]
Anderson, H
Cavallin-Ståhl, E
Dictor, M
Hagberg, H
Johnson, A
Kaasa, S
Kvaloy, S
Sundström, C
Åkerman, M
机构
[1] Univ Lund Hosp, Jubileum Inst, Dept Oncol, S-22185 Lund, Sweden
[2] Univ Lund Hosp, Jubileum Inst, Dept Canc Epidemiol, S-22185 Lund, Sweden
[3] Univ Lund Hosp, Jubileum Inst, Dept Pathol, S-22185 Lund, Sweden
[4] Univ Uppsala Hosp, Dept Oncol, S-75185 Uppsala, Sweden
[5] Univ Uppsala Hosp, Dept Pathol, S-75185 Uppsala, Sweden
[6] Norwegian Radium Hosp, Dept Oncol, Oslo, Norway
[7] Univ Trondheim Hosp, Dept Radiotherapy & Oncol, Palliat Med Unit, Trondheim, Norway
关键词
aggressive lymphoma; chemotherapy; prognostic factors; randomised trial;
D O I
10.1023/A:1008392528248
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The long-term survival of patients with advanced stage aggressive lymphoma has not improved significantly during the last twenty years. In a randomised trial, the efficacy of MACOP-B, a six-drug weekly chemotherapy regimen, was compared to CHOP, the current standard regimen, in terms of overall and failure-free survival, toxicity and health related quality of life. Patients and methods: Four hundred five patients with aggressive lymphoma, stage II-IV, age 18-67, were randomised to receive either 12 weeks of MACOP-B or 8 courses of CHOP over 24 weeks. Special emphasis was put in the definition of Ann Arbor stage in extranodal disease. A subset of 95 patients also entered a quality of life study, based on the EORTC QLQ-C30. Results: Thirty-one patients were ineligible. Among the remaining 374 patients, the median age was 52 years. According to the age-adjusted International Prognostic Index, 37% were 'high-intermediate' or `high-risk' patients. No difference could be demonstrated, either in overall survival (60% at five years in the MACOP-B group and 59% in the CHOP group) or in failure-free survival (47% at five years with MACOP-B and 44% with CHOP). In terms of quality of life, physical function and global quality of life were more impaired in patients receiving MACOP-B, who also exhibited more non-haematological toxicity. Conclusion: No superiority of MACOP-B compared to CHOP could be demonstrated. CHOP remains the treatment of choice in low-risk patients. At present, intensified or experimental treatment should be reserved for high-risk disease.
引用
收藏
页码:1079 / 1086
页数:8
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