期刊文献+

地西他滨联合减量HAD方案治疗复发难治性急性髓系白血病临床观察 被引量:11

Clinical observation of Decitabine combined with low-dose HAD regimen in treatment of relapsed or refractory acute myeloid leukemia
下载PDF
导出
摘要 目的观察地西他滨(DAC)联合减量HAD方案治疗复发难治性急性髓系白血病(AML)患者的疗效。方法回顾性分析该院16例复发难治性AML患者予以DAC 5 d联合减量HAD方案治疗的过程和转归。结果完全缓解(CR)10例(62.50%),部分缓解(PR)1例(6.25%),总有效率(ORR)为68.75%。总血液学不良反应发生率为100.00%,13例(81.25%)发生感染,3例(18.80%)发生败血症,4例(25.00%)发生轻度肝功能损害,未发生化疗相关死亡。结论 DAC联合减量HAD方案治疗复发难治性AML患者疗效较好。 [Objective ] To evaluate the efficacy and adverse reactions of Decitabine combined with low- dose HAD regimen on relapsed or refractory acute myeloid leukemia. [Methods] The clinical data of 16 diagnosed cases of relapsed or refractory acute myeloid leukemia who were treated with Decitabine combined with low-dose HAD regimen were collected and analyzed. [Resdts] Among the 16 patients, 10 (62.50%) achieved complete remission, 1 (6.25%) achieved partial remission, the total efficiency rate was 68.75%. Hematologic toxicity was 100.00%. The incidence rate of infection was 81.25% (13/16), and mild liver injury occurred in 4 eases (25.00%). Treatment-related death was not found. [Conclusion] Decitabine combined with low-dose HAD regimen can effectively treat relapsed or refractory acute myeloid leukemia.
出处 《中国现代医学杂志》 CAS 北大核心 2015年第32期75-77,共3页 China Journal of Modern Medicine
基金 荆州市医疗卫生科技计划项目(No:2014024)
关键词 急性髓系白血病 复发性/难治性 地西他滨 acute myeloid leukemia relapsed/refractory Decitabine
  • 相关文献

参考文献9

二级参考文献19

  • 1孟凡义,徐兵,杜欣,汪明春,朱康儿.氟达拉滨联合不同剂量阿糖胞苷治疗复发、难治性急性白血病86例分析[J].中华血液学杂志,2006,27(6):419-420. 被引量:14
  • 2李守娟,顾健.DNA拓扑异构酶和端粒酶与白血病多药耐药关系[J].中国实验血液学杂志,2007,15(1):207-210. 被引量:4
  • 3MOMPARLER R L. Pharmacology of 5-Aza-2'-deoxycyti- dine ( decitabine ) [ J ] . Semin Hematol, 2005, 42 (3) : 9-16.
  • 4JABBOUR E, ISSA J P, GARCIA-MANERO G, et al. Evolution of decitabine development: accomplishments, ongoing investigations, and future strategies. [ J ]. Canc- er, 2008, 112 (11): 2341-2351.
  • 5DUENAS-GONZALEZ A, CANDELARIA M, PEREZ- PLASCENCIA C, et al. Valproic acid as epigenetic cancer drug: preclinical, clinical and transcriptional effects on solid tumors [ J ]. Cancer Treat Rev, 2008, 34 (3) : 206-222.
  • 6POPOV B V, WATT S M, ROZANOV I U M, et al. A pocket pRb mutation induces the increase in its affinity to E2F4 coupled with activation of muscle differentiation [J]. Mol Biol, 2010, 44 (2): 321-325.
  • 7Harris NL, Jaffe ES, Diebold J, et al.World health organization classi fication of neoplastic diseases of the hematopoietic and lymphoid tis sue:report of the clinical advisory committee meeting-Airlie house Virginia, November 1997[J]. J Clin Oncology, 1999,17( 12 ):3835- 3849.
  • 8董玉玮,侯进慧,朱必才,等.表观遗传学的相关概念和研究进展[J].生命的化学,2005,22(1):1-3.
  • 9Jones PA,Baylin SB. The fundamental role of epigenetic events in cancer [J]. Nat Rev Genet,2002,3(6) :415-428.
  • 10Ltibbert M,Rtiter BH,Claus R,et al.A multieenter phase Ⅱ trial of decitabine as first-line treatment for older patients with acute myeloid leukemia judged unfit for induction chemotherapy [J].Hematologica, 2012,97(3 ) : 393-401.

共引文献189

同被引文献86

引证文献11

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部