抗癌药物的心血管毒性:成功的阴暗面

J. Tamargo
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摘要

在欧洲联盟,癌症是仅次于心血管疾病的第二大死因,占所有死亡人数的27%。抗癌药物(ACDs)具有较差的细胞选择性和狭窄的治疗范围,因此其血浆水平的微小增加会导致多种组织出现不良反应。fac可产生广泛的心血管不良反应(称为心脏毒性),增加发病率,甚至可导致一些癌症已被ACD治愈的患者死亡。心脏毒性的风险随着年龄的增长而增加,由于多达三分之二的癌症患者年龄超过65岁,因此随着年龄增长发病率增加的癌症、心血管疾病和cad诱导的心脏毒性将在这一人群中共存。CAFs引起的心脏毒性的诊断、预后、随访和治疗在日常临床实践中是一个挑战,这使得心脏病学家、肿瘤学家和血液学家之间的团队合作至关重要。欧洲心脏病学会最近的心脏肿瘤学指南代表了这种联合工作的第一次经验,以全面解决抗癌药物引起的心脏毒性。
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Cardiovascular toxicity of anticancer drugs: the dark side of success
Cancer represents the second cause of death in the European Union after cardiovascular diseases, accounting for 27% of all deaths. Anticancer drugs (ACDs) have poor cell selectivity and a narrow therapeutic margin, in such a way that small increases in their plasma levels lead to the appearance of adverse reactions in multiple tissues. The FACs can produce a wide range of adverse cardiovascular reactions (named cardiotoxicity) that increase morbidity and can even lead to death in some patients whose cancer has been cured by the ACD. The risk of cardiotoxicity increases with age, and since up to two-thirds of cancer patients are older than 65 years of age, cancer, cardiovascular diseases whose incidence increases with age and CAD-induced cardiotoxicity will coexist in this population. The diagnosis, prognosis, follow-up, and treatment of cardiotoxicity induced by CAFs represent a challenge in daily clinical practice that makes teamwork among cardiologists, oncologists, and hematologists essential. The recent guidelines on cardio-oncology of the European Society of Cardiology represents the first experience of this joint work to comprehensively address the cardiotoxicity due to anticancer drugs.
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