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E-CHOP方案治疗20例T细胞性非霍奇金淋巴瘤的疗效分析

E-CHOP Regimen in the Treatment for Non-Hodgkin's Lymphoma(T型)
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摘要 目的:E-CHOP方案治疗T细胞性非霍奇金淋巴瘤(T-NHL)患者的近期疗效、远期生存和不良反映。方法:回顾性分析20例T-NHL患者的临床特征及E-CHOP方案化疗加或不加局部放疗的近期疗效、不良反应及远期生存情况。结果:20例患者中,平均年龄45岁,临床分期Ⅰ-Ⅱ期3例,占15%;Ⅲ-Ⅳ期占85%,经国际预后指数(IPI)评分为3-4分者占85%,此20例患者均采用E-CHOP方案治疗,平均6-9个疗程,加或不加局部放疗,评价客观疗效,总有效率为74.3%,CR率为55%。主要不良反应为骨髓抑制;平均随访期为27个月(6-48个月),1-4年生存率分别为:60%、50%、40%、35%。结论:采用E-CHOP方案治疗T-NHL近期疗效、远期生存率较以往有提高,副作用少,价格低廉,值得临床进一步验证和推广应用。 Objective: The aim of this study is to analyse the efficacy and toxicity of E - CHOP regimen the treatment of non-Hodgkin's lymphoma(T- NHL). Methods:from may 2003 to may 2007, 20patients with T - NHL , were treated by E - chop regiment with or without radiotherapy for the involved field. The dinical cha racteristics, response, toxicity and long- term survival results were analysed retrospectively. Results:The median age was 45 (range: 18 - 62 y), All patients were treated by E - CHOP 6 -- 9, with or without radiotherapy. The overall response(OR)rate in this series was 74.3 %, with a complete remission( CR) rate of 55 %. major toxicity consisted of grade Ⅲ-Ⅳ myelosuppression ( 10 % ), neutropenia ( 35 ), and thrombocytopenia and anema ( 1.3 % ), median follow - up duration in this series was 27 months (range: 6 -48 months), the overall 1 -- 4 year survival rate was: 60 % ; 50 % ; 40 % ; 35 %. Conclusion: Our data show that E - CHOP regimen combined with or without radiotherapy for the involved field is effective and well to tolerated by the patients with T - NHL.
作者 常新东
出处 《内蒙古医学杂志》 2008年第3期293-294,共2页 Inner Mongolia Medical Journal
关键词 T-非霍奇金淋巴瘤 足叶以甙 总生存期 Non - Hodgkin' s lymphoma VP - 16 Overall survival
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参考文献2

  • 1Fisher RI. Cyclophosphamide, doxorubicin, Vineristine, and prednisone Versus intensive chemotherapy in non - Hodgkin' s lymphoma[J]. Cancer Chemother Pharmacol, 1997, 40(Supp) : S42-46.
  • 2Montserrat E, Garcia - Conde J, Vindas N, et al. CHIP VS PROMACE - cytaBOM in the treatment of aggressive non - Hodykin's lymphoma: long- term results of a multicenter randomized trial[J]. ERRJ Haematol, 1996, 57:377- 379.

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