期刊文献+

急性白血病患者化疗方案中应用力素对化疗药物急性心脏毒性的影响 被引量:2

Effect of calcium dibutyryladenosione cyclophosphate on chemotherapeutic toxicity in acute leukemia
下载PDF
导出
摘要 目的:观察急性白血病化疗患者应用力素(二丁酰环磷腺苷钙)对化疗药物急性心脏毒性的影响。方法:将初治急性白血病患者58例分成治疗组(n=28)和对照组(n=30)两组,治疗组在普通化疗方案的基础上加用力素治疗,对照组仅用普通化疗方案治疗,观察两组第二疗程化疗后心肌酶的变化、心力衰竭的发生情况、平均心率及心电图ST段的变化。结果:两组的心肌酶(磷酸肌酸激酶、乳酸脱氢酶及α羟丁酸脱氢酶)、平均心率、心电图ST段的下移的程度差异均有显著性(P<0.01或0.05);但两组的心力衰竭发生情况差异无显著性(P>0.05)。结论:力素能够减轻化疗药物对急性白血病化疗患者的急性心脏毒性。 Objective: To observe the effect of calcium dibutyryladenosine cyclophosphate (CDBAC) on chemotherapeutic toxicity in acute leukemia. Methods: Fifty-eight initial treatment patients with acute leukemia were divided into 2 groups: control group (n=30) treated with conventional chemotherapy regimen, and treatment group (n= 98) received chemotherapy and CDBAC. Myocardial enzyme, heart failure, average heart rate and ST segment were observed in two groups after two courses. Results: Except heart failure incidence, creatine phosphate kinase, lactate dehydrogenase and hydroxybutyrate dehydrogenase levels, average heart rate and ST segment descent were significantly lower in treatment group than that in control group (P〈0. 01~0.05). Conclusion: CDBAC alleviates acute heart toxicity in patients with acute leukemia during chemotherapy.
出处 《广东医学院学报》 2005年第4期382-383,共2页 Journal of Guangdong Medical College
关键词 力素 白血病 心脏 calcium dibutyrytadenosine cyctophosphate leukemia heart
  • 相关文献

参考文献7

二级参考文献14

共引文献155

同被引文献22

  • 1观美华,黄妙儿,刘鹏,钟灼,王飞,马永华,钟彩玲.柔红霉素对急性白血病患者心脏毒性的临床观察[J].中国热带医学,2006,6(4):666-667. 被引量:10
  • 2曹志红,祝焱,彭敏源.急性白血病LDH及HBDH测定的临床意义[J].实用预防医学,2007,14(2):489-490. 被引量:10
  • 3Raschi E, Vasina V, Ursino MG,et al. Anticancer drugs and cardiotoxicity:Insights and perspectives in the era of targeted therapy[ J ]. Pharmacol Ther,2010.125 (2) : 196- 218.
  • 4Giantris A,Abdurrahman L, Hinkle A, Assetin B, Lipshultz SE. Anthracycline- induced cardiotoxicity in children and young adults [J]. Crit Rev Oncol Hematol,1998,27(1):53-68.
  • 5Wouters KA, Kremer LC, Miller TL, Herman EH, Lipshuhz SE. Protecting against anthracycline- induced myocardial damage:a review of the most promising strategies [ J ]. Br J Haematol,2005,131 ( 5 ) : 561-578.
  • 6Hasinoff BB. Herman EH. Dexrazoxane :how it works in cardiac and tumor cells. Is it a prodrug or is it a drug[ J ] ? Cardiovasc Toxicol 2007,7(2):140-144.
  • 7Swain SM,Vici P. The current and future role of dexrazoxane as a cardioprotectant in anthracycline treatment:expert panel review [ J ]. J Cancer Res Clin Oncol,2004,130 ( 1 ) : 1 - 7.
  • 8Cardinale D,Colombo A, Sandri MT, et al. Prevention of high- dose chemotherapy - induced cardiotoxieity in high - risk patients by angiotensin - converting enzyme inhibition [ J ]. Circulation, 2006,114 ( 2 ) :2474- 2481.
  • 9Chen MH, Kerkel? R, Force T. Mechanisms of Cardiac Dysfunction Associated With Tyrosine Kinase Inhibitor Cancer Therapeutics [J]. Circulation,2008,118(1);84-95.
  • 10Seidman A ,Hudis C, Pierri MK, et al. Cardiac Dysfunction in the Trastuzumab Clinical Trials Experience [ J ]. J Clin Oncol, 2002, 20 (5) :1215-1221.

引证文献2

二级引证文献7

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