期刊文献+

DA与MA方案诱导治疗急性髓系白血病的疗效分析 被引量:4

Therapeutic effect of DA regimen and MA regimen on the first treatment for acute myeloid leukemia
原文传递
导出
摘要 目的比较柔红霉素联合阿糖胞苷(DA方案)与米托蒽醌联合阿糖胞苷(MA方案)诱导治疗初发急性髓系白血病的临床疗效及不良反应。方法将2010年6月至2013年7月68例初诊为急性髓系白血病的患者,随机给予DA方案组(36例)或MA方案组(32例)诱导化疗1个疗程,比较DA方案组与MA方案组的完全缓解率、总有效率及不良反应发生率。结果DA方案组完全缓解(CR)18例(50%),部分缓解(PR)3例(8.3%),总有效率为58.3%(21/36)。MA方案组CR23例(71.2%),PR4例(12.5%),总有效率为84.4%(27/32),两组方案总有效率比较差异有统计学意义(P〈0.05)。MA方案组心脏毒性发生率低于DA方案组,骨髓抑制重于DA方案组。结论MA方案组的疗效优于DA方案组。 Objective To compare the safety and side effects of daunorubicin + cytosine arabinoside( DA regimen) and mitoxantrone + cytosine arabinoside ( MA regimen) for the first diagnosed acute myeloid leukemia(AML) patients. Methods Sixty-eight patients with acute myeloid leukemia from June 2010 to July 2013 were randomly divided into two groups, including 36 cases with DA regimen and 32 cases with MA regimen. The complete response rate, overall response rate, side effect rate were compared separately. Results In the DA group and the MA group, the rate of complete response, partial re- sponse, and overall response was 50% (18/36) vs. 71.2% (23/32), 8.3% (3/36) vs. 12.5% (4/32), 58.3% (21/36) vs. 84. 4% (27/32) respectively. There were significant differences between the two groups in the overall response rates ( P 〈 0. 05 ) . The cardiotoxicity incidence of MA group was lower than that of DA group, while bone marrow suppression was heavier than that of DA group. Conclusions MA regimen is superior to DA regimen.
作者 李春霞
出处 《中国实用医刊》 2014年第6期67-69,共3页 Chinese Journal of Practical Medicine
关键词 急性髓系白血病 米托蒽醌 柔红霉素 阿糖胞苷 Acute myeloid leukemia Mitoxantrone Daunorubicin Cytosine arabinoside
  • 相关文献

参考文献13

二级参考文献63

共引文献320

同被引文献41

  • 1高文斌,于克达,王丽双,王蕾,尹良伟.表阿霉素大剂量持续静滴对心脏毒性反应的观察[J].药物不良反应杂志,2005,7(1):15-17. 被引量:4
  • 2刘陶文.蒽环类药对心脏的毒性反应及其保护措施[J].癌变·畸变·突变,2006,18(2):156-158. 被引量:3
  • 3李莉霞,唐跃年.阿糖胞苷抗白血病药理作用及耐药机制研究进展[J].中国药房,2006,17(19):1506-1507. 被引量:6
  • 4范冬梅,高瀛岱,杨铭,邵晓枫,王金宏,纪庆,许元富,熊冬生,杨纯正.阿糖胞苷上调耐药白血病细胞共刺激分子表达及其分子机制研究[J].中华微生物学和免疫学杂志,2007,27(9):815-818. 被引量:3
  • 5张之男,沈悌.血液病诊断及疗效标准[M].第3版.北京:科学出版社,2008:106-134.
  • 6Lowenberg B, Ossenkoppele G J, van Putten W, et al.High- dose daunorubicin in older patients with acute myeloid leukemia[J]. N Engl J Med, 2009, 361 ( 13 ) : 1235-1248.
  • 7Kolitz JE, George SL, Dodge RK, et al.Dose escalation studies ofcytarabine, daunorubicin, and etoposide with and without multidrugresistance modulation with PSC-833 in untreated adults with acute my-eloid leukemia younger than 60 years : final induction results of Cancerand Leukemia Group B Study 9621[J].J Clin Oncol, 2004,22 ( 21 ) : 429-430.
  • 8Bozoglan H, Ergene U, Yoleri L, et al.Use of cytarabine and ida-rubicin in a newly diagnosed AML patient with a severe wound[J].Transfus Apher Sci, 2011,45 ( 1 ) : 17-20.
  • 9Simfiek, st6rba, Popelovi O, et al. Anthracycline-induced cardiotoxicity: Overiew of studies examining the roles of oxidative stress and free cellular iron[J].Pharmacol Rep, 2009,61(1 ) : 154.
  • 10Kim SY, Kim S J, Kim B J, et al. Doxorubicin induced re- active oxygeny species generation and intracellular Caz + increanse are reciprocally modulated in rat cardiomyo- cytes[J]. Exp Mol Med, 2006,38 (5) : 535.

引证文献4

二级引证文献17

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