期刊文献+

稳心颗粒配合右丙亚胺防治表柔比星心脏毒性的临床观察 被引量:9

Wenxinkeli combined with dexrazoxane in the prevention of epirubicin-induced cardiotoxicity
暂未订购
导出
摘要 目的:探讨稳心颗粒配合右丙亚胺对表柔比星所致心脏毒性的防治作用。方法:观察116例应用含表柔比星方案化疗的患者,以心电图的变化作为观察指标。先单独化疗4个周期,然后将已出现心电图异常者归入稳心颗粒配合右丙亚胺化疗组,心电图正常者分为单独化疗组与稳心颗粒配合右丙亚胺联合化疗组继续化疗2个周期,观察心电图变化。结果:单独化疗4个周期过程中,心电图异常发生率分别为24.1%(28/116)。继续化疗2个周期,单独化疗组心电图异常发生率分别为40.4%(21/52),稳心颗粒配合右丙亚胺化疗组心电图异常发生率为19.2%(10/52),(P<0.05),差异有统计学意义;稳心颗粒配合右丙亚胺治疗组有17.9%(5/28)患者异常心电图转为正常,有28.6%(8/28)患者异常心电图保持稳定,其余53.6%患者心脏损害加重。结论:稳心颗粒配合右丙亚胺对表柔比星所致心脏毒性的发生有一定的防治作用,使更多病人延长表阿霉素的治疗,并且对已经形成的心脏损害有一定的修复作用。 Objective:To investigate the protective effects of Wenxinkeli with dexrazoxane on epirubicin cardiotoxicity.Methods:After four cycles of chemotherapyalone,116 patients were classified as a chemotherapy group and the Wenxinkeli with dexrazoxane combined with chemotherapygroup to observe the ECG changes after 2 cycles.Results:After four-cycles of chemotherapy alone,ECG abnormal incidence was 24.1%(28/116).To proceed two cycles of chemotherapy,the incidence of ECG abnormalities was 40.4%(21/52)in chemotherapy alone group and 19.2%(10/52)in the Wenxinkeli with dexrazoxane combined group.The difference was significant(P0.05).In Wenxinkeli with dexrazoxane treatment group,there was 17.9%(5/28)patients whose ECG charged from abnormal to normal,and 28.6%(8/28)remained stable.The heart damage of remaining 53.6%patients increased.Conclusion:Wenxinkeli combined with dexrazoxane not only has cardiao-protective activtyagainst cardio-toxicity induced and enable more patients to extend the treatment of epirubicin by epirubicin but also has some therapeutic effect.
作者 赵文娟 赵伟 Zhao Wenjuan;Zhao Wei(Emergency Department Southern Medical University,Hengyang Central Hospital Hunan Hengyang 421001 China;Department ofMedical Oncology,First Affiliated Hospital of China Medical University,Liaoning Shenyang 110001,China)
出处 《现代肿瘤医学》 CAS 2013年第7期1623-1625,共3页 Journal of Modern Oncology
关键词 右丙亚胺 表柔比星 心脏毒性 dexrazoxane epirubicin cardiac toxicity
  • 相关文献

参考文献20

  • 1Blowers E, Hall K. Managing adverse events in the use of bevaci- zumab and cheroot herapy [ J ]. Nurs,2009,18 (6) :351 - 356.
  • 2Jones AL, Barlow M, Barrett - Lee PJ. Management of cardiac health in trastuzumab -treated patients with breast cancer: upda- ted United Kingdom National Cancer Research Institute recom- mendations for monitoring [ J ]. Cancer,2009,100 ( 5 ) :684 - 692.
  • 3罗群,陈素芬,蒲小燕,余萍.恶性淋巴瘤阿霉素化疗的心电图分析[J].实用心电学杂志,2008,17(6):419-420. 被引量:9
  • 4Lipshultz SE, Rifai N, Dalton VM, et al. The effect of dexrazoxane on myocardial injury in doxombicin -treated children with acute lympho - blastic leukemia [ J ]. N Engl J Med, 2004,351 ( 2 ) : 145 - 153.
  • 5吕俊,丁念,朱家蔷,高霞.蒽环类药物心脏毒性及其预防的研究进展[J].中国医院药学杂志,2008,28(15):1302-1303. 被引量:19
  • 6Chakrabarti KB, Hopewell JW, Wilding D, et al. Modification of doxorubicin- induced cardiotoxicity: effect of essential fatty acids and ICRF - 187 (dexrazoxane) [ J ]. Eur J Cancer,2001,37 ( 11 ) : 1435 - 1442.
  • 7Sromova T, Strnadova V, Hrstkova H. Monitoring cardiotoxicity of anthracyclines in children and possibilities of its prevention [ J ]. Vnitr Lek,2002,48 (7) :649 - 656.
  • 8Simunek T, Klimtova I, Kaplanova J, et al. Rabbit model for in vivo study of anthracycline - induced heart failure and for the evaluation of protective agents [ J ]. Eur J Heart Fail,2004,6 (4) : 377 - 387.
  • 9Lebrecht D, Geist A, Ketelsen UP, et al. Dexrazoxane prevents doxorubicin - induced long - term cardiotoxicity and protects myo- cardial mitoehondria from genetic and functional lesions in rats [J]. Br J Pharmacol,2007,151 (6) :771 -778.
  • 10Plande J, Plate1 D, Tariosse L, et al. Experimental study of dexrazoxane - anthracycline combinations using the modal of iso- lated perfused rat heart [ J ]. Toxicol Lett,2006,161 ( 1 ) : 37 - 42.

二级参考文献36

共引文献43

同被引文献80

  • 1吴晓明,胡承章,李宁,朱继庆,吴艳芳.血清CK-MB与晚期肿瘤患者心功能的相关性及其对预后的判断[J].癌症,2005,24(4):506-508. 被引量:14
  • 2Sant M, AUemani C, Santaquilani M, et al. EUROCARE--4. Sur- vival of cancer patients diagnosed in 1995-1999. Restflts and com- mentary[J]. EurJ Cancer, 2009, 45(6):931-991.
  • 3Oeffmger KC, Mertens AC, Sklar CA, et al. Chronic health condi- tions in adult survivors of childhood cancer[J]. N EnglJ Med, 2006, 355 (15) :1572-1582.
  • 4Geiger S, Lange V, Suhl P, et al. Anticancer therapy induced cardio- toxicity: review of the literature[J]. Anticancer Drugs, 2010, 21(6): 578-590.
  • 5Jirkovsky E, Popelova O, Krivakova-Stankova P, et al. Chronic an- thracycline cardiotoxicity: molecular and functional analysis with fo- cus on nuclear factor erythroid 2-related factor 2 and mitochondri- al biogenesis pathways[J]. J Pharmacol Exp Ther, 2012, 343(2): 468-478.
  • 6Swain SM, Whaley FS, Ewer MS. Congestive heart failure in pa- tients treated with doxorubicin: a retrospective analysis of three tri- als[J]. Cancer, 2003, 97(11):2869-2879.
  • 7Zuppinger C, Timolati F, Suter TM. Pathophysiology and diagno- sis of cancer drug induced cardiomyopathy[J]. Cardiovasc Toxicol, 2007, 7(2):61-66.
  • 8Octavia Y, Tocchetti CG, Gabrielson KL, et al. Doxorubicin-in- duced cardiomyopathy: from molecular mechanisms to therapeutic strategies[J].J Mol Cell Cardiol, 2012, 52(6):1213-1225.
  • 9Sterba M, Popelova O, Vavrova A, et al. Oxidative stress, redox signaling, and metal chelation in anthracycline cardiotoxicity and pharmacological cardioprotection[J]. A Antioxid Redox Signal, 2013, 18(8) :899-929.
  • 10Gammella E, Maccarinelli F, Buratti P, et al. The role of iron in an- thracycline cardiotoxicity[J]. Front Pharmacol, 2014, 5 (25):1-6.

引证文献9

二级引证文献48

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