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[化疗药物诱发的心力衰竭]

[Chemotherapeutics-induced heart failure].

作者信息

Paulides Marios, Wojnowski Leszek

机构信息

Late Effects Surveillance System Studienleitung, Kinder- und Jugendklinik, Universitätsklinikum Erlangen, Erlangen.

出版信息

Med Klin (Munich). 2007 Jul 15;102(7):574-8. doi: 10.1007/s00063-007-1071-y.

DOI:10.1007/s00063-007-1071-y
PMID:17634876
Abstract

BACKGROUND

Antineoplastic chemotherapy may induce acute or late side effects. Cytostatic-induced cardiomyopathy counts as one of the most dangerous side effects and has major implications for the use of anthracyclines. Since anthracyclines are widely employed and frequently indispensable cytostatics, it is important to elucidate the mechanisms and risk factors of the associated heart failure and develop preventive or interventional strategies.

RESULTS

Anthracycline-induced cardiomyopathy has been reported in up to 85% of treated patients. Known risk factors are younger age, advanced age, female gender, preexisting cardiac illness, cardiac irradiation, and other concomitant cardiotoxic medications. Proposed preventive strategies include the development of new anthracyclines, longer anthracycline infusion times, liposomal anthracycline formulations, the application of the iron chelator dexrazoxane, and identification of predisposing gene variants.

CONCLUSION

Most promising preventive strategies include longer infusion times, liposomal formulations, and the administration of the iron chelator dexrazoxane.

摘要

背景

抗肿瘤化疗可能会引发急性或晚期副作用。细胞毒性药物诱发的心肌病是最危险的副作用之一,对蒽环类药物的使用有重大影响。由于蒽环类药物是广泛应用且常常不可或缺的细胞毒性药物,阐明相关心力衰竭的机制和危险因素并制定预防或干预策略很重要。

结果

据报道,接受治疗的患者中高达85%出现蒽环类药物诱发的心肌病。已知的危险因素包括年龄较小、年龄较大、女性、原有心脏疾病、心脏放疗以及其他伴随的心脏毒性药物。提议的预防策略包括开发新的蒽环类药物、延长蒽环类药物输注时间、脂质体蒽环类药物制剂、应用铁螯合剂右丙亚胺以及识别易感基因变异。

结论

最有前景的预防策略包括延长输注时间、脂质体制剂以及给予铁螯合剂右丙亚胺。

相似文献

1
[Chemotherapeutics-induced heart failure].[化疗药物诱发的心力衰竭]
Med Klin (Munich). 2007 Jul 15;102(7):574-8. doi: 10.1007/s00063-007-1071-y.
2
Exposure to anthracyclines during childhood causes cardiac injury.儿童时期接触蒽环类药物会导致心脏损伤。
Semin Oncol. 2006 Jun;33(3 Suppl 8):S8-14. doi: 10.1053/j.seminoncol.2006.04.019.
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Br J Haematol. 2005 Dec;131(5):561-78. doi: 10.1111/j.1365-2141.2005.05759.x.
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Anthracycline-induced cardiomyopathy.蒽环类药物诱导的心肌病。
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Semin Oncol. 1998 Oct;25(5):525-37.
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Evaluating the role of dexrazoxane as a cardioprotectant in cancer patients receiving anthracyclines.评估右丙亚胺在接受蒽环类药物治疗的癌症患者中作为心脏保护剂的作用。
Cancer Treat Rev. 2004 Nov;30(7):643-50. doi: 10.1016/j.ctrv.2004.06.002.
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Pathophysiology and diagnosis of cancer drug induced cardiomyopathy.癌症药物性心肌病的病理生理学与诊断
Cardiovasc Toxicol. 2007;7(2):61-6. doi: 10.1007/s12012-007-0016-2.
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Cardiotoxic consequences of anthracycline-containing therapy in patients with breast cancer.含蒽环类药物治疗对乳腺癌患者的心脏毒性后果。
Semin Oncol. 2006 Jun;33(3 Suppl 8):S15-21. doi: 10.1053/j.seminoncol.2006.04.022.
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Pharmacologic prevention of anthracycline-induced cardiomyopathy.蒽环类药物诱导的心肌病的药物预防
Cardiol Rev. 2009 Sep-Oct;17(5):243-52. doi: 10.1097/CRD.0b013e3181b8e4c8.
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Genotyping the risk of anthracycline-induced cardiotoxicity.对蒽环类药物引起心脏毒性的风险进行基因分型。
Cardiovasc Toxicol. 2007;7(2):129-34. doi: 10.1007/s12012-007-0024-2.

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