GDP与CHOP方案治疗非特异性外周T细胞淋巴瘤的疗效分析

张明智 邢朋涛 李玲

张明智, 邢朋涛, 李玲. GDP与CHOP方案治疗非特异性外周T细胞淋巴瘤的疗效分析[J]. 中国肿瘤临床, 2012, 39(12): 857-860. doi: 10.3969/j.issn.1000-8179.2012.12.011
引用本文: 张明智, 邢朋涛, 李玲. GDP与CHOP方案治疗非特异性外周T细胞淋巴瘤的疗效分析[J]. 中国肿瘤临床, 2012, 39(12): 857-860. doi: 10.3969/j.issn.1000-8179.2012.12.011
Mingzhi ZHANG, Pengtao XING, Ling LI. GDP and CHOP Chemotherapy for Nonspecific Peripheral T-cell Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(12): 857-860. doi: 10.3969/j.issn.1000-8179.2012.12.011
Citation: Mingzhi ZHANG, Pengtao XING, Ling LI. GDP and CHOP Chemotherapy for Nonspecific Peripheral T-cell Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(12): 857-860. doi: 10.3969/j.issn.1000-8179.2012.12.011

GDP与CHOP方案治疗非特异性外周T细胞淋巴瘤的疗效分析

doi: 10.3969/j.issn.1000-8179.2012.12.011
详细信息
    通讯作者:

    李玲  E-mail: lingl510@126.com

GDP and CHOP Chemotherapy for Nonspecific Peripheral T-cell Lymphoma

More Information
  • 摘要:   目的  探讨GDP方案和CHOP方案治疗非特异性外周T细胞淋巴瘤(PTCL-U)的疗效和安全性。  方法  回顾性分析自2008年1月至2011年12月郑州大学第一附属医院淋巴瘤诊疗中心收治经病理学确诊的PTCL-U患者29例。14例患者应用GDP方案,15例应用CHOP方案。采用χ2检验和Log-Rank检验,对两组的疗效及不良反应进行分析和比较。  结果  接受GDP方案化疗的非特异性外周T细胞淋巴瘤患者总有效率(RR)为78.57%,而CHOP组为60.00%,两组比较差异有统计学意义(P < 0.05)。GDP组无进展生存期(PFS)为9.79个月,总生存期(OS)为17.36个月;CHOP组PFS为4.2个月,OS为11.27个月,两组比较差异均有统计学意义(P < 0.05)。主要不良反应为血液学毒性,其中GDP方案Ⅲ~Ⅳ度血液学毒性发生率57.14%,CHOP方案Ⅲ~Ⅳ度血液学毒性为33.33%。  结论  GDP方案治疗外周T细胞淋巴瘤疗效优于传统CHOP方案,虽然血液学毒性稍重,仍值得临床推广,并有望成为PTCL治疗的一线方案。

     

  • 表  1  GDP组与CHOP组病例资料  例

    Table  1.   Clinical data of the GDP and CHOP patients

    表  2  GDP组与CHOP组治疗PTCL临床疗效分析  例(%)

    Table  2.   Clinical effects of the GDP and the CHOP regimens on the PTCL patients

    表  3  GDP组与CHOP组治疗PTCL远期疗效分析  月

    Table  3.   Long-term efficacy of the GDP and the CHOP treatments for PTCL

    表  4  GDP组与CHOP组患者分期与疗效  例(%)

    Table  4.   Staging and curative effects among the patients in the GDP and the CHOP groups

    表  5  GDP组与CHOP组不良反应对比  例(%)

    Table  5.   Comparison of adverse effects between the GDP and the CHOP groups

  • [1] Straus DJ, Johnson JL, LaCasce AS, et al. Doxorubicin, vinblastine, and gemcitabine (CALGB 50203) for stage Ⅰ/Ⅱ nonbulky Hodgkinlymphoma: pretreatment prognostic factors and interim PET[J]. Blood, 2011, 117(20): 5314-5320. doi: 10.1182/blood-2010-10-314260
    [2] Piccaluga PP, Agostinelli C, Gazzola A, et al. Prognostic markers in peripheral T-cell lymphoma[J]. Curr Hematol Malig Rep, 2010, 5 (4): 222-228. doi: 10.1007/s11899-010-0062-x
    [3] Howman RA, Prince HM. New drug therapies in peripheral T-cell lymphoma[J]. Expert Rev Anticancer Ther, 2011, 11(3): 457-472. doi: 10.1586/era.11.4
    [4] Zelenetz AD, Abramson JS, Advani RH, et al. NCCN Clinical Practice Guidelines in Oncology: non-Hodgkin's lymphomas[J]. J Natl Compr Canc Netw, 2010, 8(3): 288-334. doi: 10.6004/jnccn.2010.0021
    [5] Kitagawa J, Hara T, Tsurumi H, et al. Serum-soluble interleukin-2 receptor (sIL-2R) is an extremely strong prognostic factor for patientswith peripheral T-cell lymphoma, unspecified (PTCL-U)[J]. J Cancer Res Clin Oncol, 2009, 135(1): 53-59. doi: 10.1007/s00432-008-0440-0
    [6] Foss FM, Zinzani PL, Vose JM, et al. Peripheral T-cell lymphoma [J]. Blood, 2011, 117(25): 6756-6767. doi: 10.1182/blood-2010-05-231548
    [7] Yi S, An G, Qi J, et al. The significance of bone marrow involvement in aggressive lymphomas: A retrospectivecomparison of clinical outcomes between peripheral T cell lymphoma and diffuse large B celllymphoma in China[J]. Acta Haematol, 2010, 124(4): 239-244. doi: 10.1159/000321544
    [8] Fujiwara SI, Yamashita Y, Nakamura N, et al. High-resolution analysis of chromosome copy number alterations in angioimmunoblastic T-celllymphoma and peripheral T-cell lymphoma, unspecified, with single nucleotide polymorphism-typing microarrays[J]. Leukemia, 2008, 22(10): 1891-1898. doi: 10.1038/leu.2008.191
    [9] 黄慧强, 彭玉龙, 林旭滨, 等. CHOP方案治疗106例外周T细胞淋巴瘤的临床长期随访结果分析[J]. 癌症, 2004, 23(11): 1443-1447. https://www.cnki.com.cn/Article/CJFDTOTAL-AIZH2004S1017.htm
    [10] Vose JM. The International PTCL Project. International peripheral T-cell lymphoma(PTCL) clinical and pathologic review project: poor outcome by prognostic indices and lack of efficacy with anthracyelines[J]. Blood, 2005. 106: 811. doi: 10.1182/blood.V106.11.811.811
    [11] Escalón MP, Liu NS, Yang Y, et al. Prognostic factors and treatment of patients with T-cell non-Hodgkin lymphoma: the M. D. Anderson Cancer Center experience[J]. Cancer, 2005, 103(10): 2091-2098. doi: 10.1002/cncr.20999
    [12] Zinzani PL, Venturini F, Stefoni V, et al. Gemcitabine as single agent in pretreated T-cell lymphoma patients: evaluation of the long-termoutcome[J]. Ann Oncol, 2010, 21(4): 860-863. doi: 10.1093/annonc/mdp508
    [13] Martínez-Delgado B, Cuadros M, Honrado E, et al. Differential expression of NF-kappaB pathway genes among peripheral T-cell lymphomas[J]. Leukemia, 2005, 19(12): 2254-2263. doi: 10.1038/sj.leu.2403960
    [14] 张明智, 邱亚娟, 李文才, 等. 6例皮下脂膜炎样T细胞淋巴瘤临床病理特征及治疗分析[J]. 中国肿瘤临床, 2011, 38(18): 1111-1113. doi: 10.3969/j.issn.1000-8179.2011.18.014
  • 加载中
表(5)
计量
  • 文章访问数:  29
  • HTML全文浏览量:  3
  • PDF下载量:  0
  • 被引次数: 0
出版历程
  • 收稿日期:  2012-01-20
  • 修回日期:  2012-04-23

目录

    /

    返回文章
    返回