期刊文献+

地西他滨联合预激方案和传统治疗方案治疗老年MDS/MPD转化的急性髓系白血病的疗效和安全性的比较研究 被引量:26

Comparison analysis of decitabine combined with priming regimen and traditionally therapeutic regimens in treating elderly transformed acute myeloid leukemia
原文传递
导出
摘要 目的:对地西他滨联合预激方案和传统治疗方案治疗老年骨髓增生异常综合征(MDS)或骨髓增殖性疾病(MPD)转化的急性髓系白血病(AML)的有效性和安全性进行比较研究。方法:回顾性分析28例MDS/MPD转化的老年AML患者的临床资料,分别应用地西他滨联合预激方案11例和传统治疗方案17例(其中"3+7"标准方案8例、CAG方案6例及支持治疗3例),比较分析2组患者的临床疗效及不良反应。结果:地西他滨联合预激组中完全缓解(CR)7例(63.6%),未缓解(NR)4例(36.4%),总有效率(ORR)为63.6%;传统治疗组中CR 4例(23.5%),分别为"3+7"标准方案2例、CAG方案2例,NR 13例(76.5%),ORR为23.5%。地西他滨联合预激组的有效率明显高于传统治疗组,差异有统计学意义(P<0.05)。2组患者治疗前骨髓原始细胞数对于缓解与否无差异(P>0.05)。2组患者出现的不良反应主要是骨髓抑制、肺部感染、恶心呕吐、肝功能损害和心力衰竭,经过输血和抗感染等支持治疗均可以耐受,2组不良反应发生率比较差异无统计学意义(P>0.05)。随访至2013年9月,地西他滨联合预激组和传统治疗组的中位生存分别是15个月和2个月,差异有统计学意义(P<0.05)。结论:地西他滨联合预激方案治疗老年转化性AML患者的临床疗效显著,不良反应可以耐受,可作为老年转化性AML的首选方案。 Objective:To compare the clinical efficacy and safety between decitabine combined with priming regiment and traditionally therapeutic regiments in treating elderly MDS/MPD-transformed acute myeloid leukemia(AML).Method:A total of 28elderly AML patients with antecedent hematologic disorders(MDS/MPD)were en-rolled.Eleven patients received decitabine combined with priming regimen and other 17patients received tradition-ally therapeutic regiments(including 8patients with "3+7" regiment,6cases with CAG regiment and 3cases with supportive care).We analyzed the difference of clinical outcomes and adverse reactions among the two groups.Re- sult:In decitabine treatment group,7patients achieved complete remission(CR)and 4cases had no response(NR),with a total remission rate(ORR)of 63.6%;while in traditional therapy group,ORR was only 23.5%(4 cases achieved CR),including 2patients with "3+7" regimen and 2with CAG regimen.The ORR of decitabine group was significantly higher than that of traditional therapy group(P0.05).Compared with those in non-CR patients,the marrow blast counts in CR patients had no significant difference in both decitabine treatment group and traditional therapy group(P0.05).Adverse events in the two groups were similarly,mainly myelosuppres- sion,pulmonary infection,nausea,vomiting,liver injuryand heart failure could be well tolerated after managements(P〈0.05).Followed-up to September 2013,the median overall survival of decitabine group and traditional therapy group was 15and 2months respectively(P〉0.05).Conclusion:Decitabine combined with priming regimen is ef- fective and well tolerated in elderly transformed AML.
出处 《临床血液学杂志》 CAS 2014年第1期15-18,共4页 Journal of Clinical Hematology
基金 国家自然科学基金(No:81101793)
关键词 地西他滨 转化性 白血病 髓系 急性 老年 decitabine transformed acute myeloid leukemia elderly patients
作者简介 通信作者:王黎,E-mail:wl_wangdong@126.com
  • 相关文献

参考文献10

  • 1PEYRADE F, GASTAUD L, RE D, et al. Treatmentdecisions for elderly patients with haematological ma- lignancies= a dilemma [J]. Lancet Oncol, 2012, 13: e344--e352.
  • 2赵冰冰,朱正,许彭鹏,李军民,沈志祥,赵维莅,王黎.老年急性髓系白血病非遗传学预后因素分析[J].中华血液学杂志,2013,34(1):3-7. 被引量:20
  • 3KANTARJIAN H M, THOMAS X G, DMOSZYNS KA A, et al. Multicenter, randomized, open label, phase III trial of decitabine versus patient choice, with physician advice, of either supportive care or low-dose cytarabine for the treatment of older patients with newly diagnosed acute myeloid leukemia [J]. J Clin Oncol, 2012,30 : 2670 - 2677.
  • 4QIAN S X,ZHANG R,ZHU Y,et al. Decitabine,low- dose cytarabine and aclarubicin combination with granulocyte colony stimulating factor priming for the induction chemotherapy of older patients with myelo- dysplastic syndromes and acute myeloid leukemia[Ab- strct]. 2012 ASH.
  • 5O'DONNELL M R, ABBOUD C N, ALTMAN J K, et al. The NCCN clinical practice guidelines in oncology (NCCN Guidelines TM) Acute myeloid leukemia[EB/ OL]. (2012-05-25). http ://www. nccnorg/profession als/physician_gls/pdf/amlpdf.
  • 6王黎,沈志祥.老年急性髓系白血病的特点和治疗策略[J].中华血液学杂志,2013,34(1):76-79. 被引量:39
  • 7JIANG Y, DUNBAR A, GONDEK L P, et al. Aber- rant DNA methylation is a dominant mechanism in progression to AML[J]. Blood, 2009, 113: 1315- 1325.
  • 8赵佑山,杨瑞,顾树程,郭娟,张曦,吴凌云,李晓,常春康.骨髓增生异常综合征患者p73基因启动子区域异常甲基化的研究[J].中华血液学杂志,2012,33(10):847-851. 被引量:8
  • 9FERRARA F. Conventional chemotherapy or hypom- ethylating agents for older patients with acute myeloid leukaemia? [J]. Hematol Oncol,2013 Mar 20. doi: 10. 1002/hon. 2046. [Epub ahead of print].
  • 10BLUM W,GARZON R,KLISOVIC R B,et al. Clinical response and miR-29b predictive significance in older AML patients treated with a 10-day schedule of decit- abine[J]. Proc Natl Acad Sci U S A, 2010, 107: 7473--7478.

二级参考文献55

  • 1Tefferi A, Vardiman JW. Myelodysplastic syndromes. N Engl J Med, 2009,361 : 1872-1885.
  • 2Jiang Y, Dunbar A, Gondek LP, et al. Aberrant DNA methylation is a dominant mechanism in MDS progression to AML. Blood, 2009, 113:1315-1325.
  • 3Galm O, Wilop S, Reicheh J, et al. DNA methylation changes in multiple myeloma. Leukemia,2004, 18: 1687-1692.
  • 4Martinez-Delgado B, Melendez B, Cuadros M, et al. Frequent inactivation of the p73 gene by abnormal methylation or LOH in non-Hodgkin' s lymphomas. Int J Cancer, 2002, 102 : 15-19.
  • 5Siu LLP, Chan JKC, Wong KF, et al. Specific patterns of gene methylation in natural killer cell lymphomas: p73 is consistently involved. Am J Pathol, 2002, 160:59-66.
  • 6Valent P, Horny HP, Bennett JM, et al. Definitions and standards in the diagnosis and treatment of the myelodysplastic syndromes: consensus statements and report from a working conference. Leuk Res, 2007, 31:727-736.
  • 7Vardiman JW, Harris NL, Brunning RD. The World Health Organization (WHO) classification of the mye[oid neoplasms. Blood, 2002, 100: 2292-2302.
  • 8Greenberg P, Cox C, LeBeau MM, et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood, 1997, 89:2079.
  • 9Ekmekci CG, Gutierrez MI, Siraj AK, et al. Aberrant methylation of multiple tumor suppressor genes in acute myeloid leukemia. Am J Hematol, 2004, 77:233-240.
  • 10Dominguez G, Garcia JM, Pena C, et al. Delta TAp73 upregulation correlates with poor prognosis in human tumors: putative in vivo network involving p73 isoforms, p53, and E2F-1. J Clin Oncol, 2006, 24: 805-815.

共引文献61

同被引文献168

引证文献26

二级引证文献164

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