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

CHOP versus MACOP-B in aggressive lymphoma--a Nordic Lymphoma Group randomised trial.
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CHOP 与 MACOP-B 治疗侵袭性淋巴瘤——北欧淋巴瘤组随机试验。

DOI:
10.1023/a:1008392528248
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发表时间:
1999
期刊:
Annals of oncology : official journal of the European Society for Medical Oncology
影响因子:
--
通讯作者:
M. Åkerman
M. Åkerman
中科院分区:
--
文献类型:
--
作者:
M. Jerkeman;H. Anderson;E. Cavallin;M. Dictor;H. Hagberg;A. Johnson;S. Kaasa;S. Kvaløy;C. Sundström;M. Åkerman

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背景 在过去的二十年中,晚期侵袭性淋巴瘤患者的长期生存率没有显著提高。在一项随机试验中,将MACOP-B(一种每周6次的化疗方案)的疗效与CHOP(目前的标准方案)在总体和无失败生存期、毒性和健康相关生活质量方面进行了比较。 患者和方法 405例侵袭性淋巴瘤患者,II-IV期,年龄18-67岁,随机接受12周MACOP-B或8个疗程CHOP治疗24周。特别强调了结节病安阿伯期的定义。95名患者的子集也进入了基于EORTC QLQ-C30的生活质量研究。 结果 31例患者不合格。在其余374例患者中,中位年龄为52岁。根据年龄调整的国际预后指数,37%的患者为“高-中等”或“高风险”患者。无论是总生存率(MACOP-B组5年时为60%,CHOP组为59%)还是无失败生存率(MACOP-B组5年时为47%,CHOP组为44%)均无差异。在生活质量方面,接受MACOP-B的患者的身体功能和整体生活质量受损更严重,这些患者也表现出更多的非血液学毒性。 结论 未证明MACOP-B与CHOP相比具有优效性。CHOP仍然是低风险患者的治疗选择。目前,强化或实验性治疗应保留给高危疾病。
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.
DOI: --
发表时间: 1971-11
期刊: Cancer research
影响因子: 11.2
作者:
P. Carbone;H. Kaplan;K. Musshoff;D. Smithers;M. Tubiana
通讯作者: P. Carbone;H. Kaplan;K. Musshoff;D. Smithers;M. Tubiana
DOI: 10.1056/nejm199211053271903
发表时间: 1992-11-05
影响因子: 158.5
作者:
GORDON, LI;HARRINGTON, D;OCONNELL, M
通讯作者: OCONNELL, M
DOI: 10.1200/jco.1990.8.6.963
发表时间: 1990-06-01
影响因子: 45.3
作者:
KWAK, LW;HALPERN, J;HORNING, SJ
通讯作者: HORNING, SJ
DOI: 10.1056/nejm199304083281404
发表时间: 1993-04-08
影响因子: 158.5
作者:
FISHER, RI;GAYNOR, ER;MILLER, TP
通讯作者: MILLER, TP