Floyd Justin D, Nguyen Duc T, Lobins Raymond L, Bashir Qaiser, Doll Donald C, Perry Michael C
University of Missouri-Columbia, Ellis Fischel Cancer Center, 115 Business Loop 70 W, Columbia, MO 65203, USA.
J Clin Oncol. 2005 Oct 20;23(30):7685-96. doi: 10.1200/JCO.2005.08.789.
Because cancer is a leading cause of mortality in the United States, the number of therapeutic modalities available for the treatment of neoplastic processes has increased. This has resulted in a large number of patients being exposed to a wide variety of cancer therapy. Historically, it has been well recognized that antineoplastic agents may have adverse effects on multiple organs and normal tissues. The most commonly associated toxicities occur in tissues composed of rapidly dividing cells and may spontaneously reverse with minimal long-term toxicity. However, the myocardium consists of cells that have limited regenerative capability, which may render the heart susceptible to permanent or transient adverse effects from chemotherapeutic agents. Such toxicity encompasses a heterogeneous group of disorders, ranging from relatively benign arrhythmias to potentially lethal conditions such as myocardial ischemia/infarction and cardiomyopathy. In some instances, the pathogenesis of these toxic effects has been elucidated, whereas in others the precise etiology remains unknown. We review herein the various syndromes of cardiac toxicity that are reported to be associated with antineoplastic agents and discuss their putative mechanisms and treatment.
由于癌症是美国主要的死亡原因之一,可用于治疗肿瘤过程的治疗方式数量有所增加。这导致大量患者接触到各种各样的癌症治疗方法。从历史上看,人们已经充分认识到抗肿瘤药物可能对多个器官和正常组织产生不良影响。最常见的相关毒性发生在由快速分裂细胞组成的组织中,并且可能在最小的长期毒性作用下自发逆转。然而,心肌由再生能力有限的细胞组成,这可能使心脏易受化疗药物的永久性或暂时性不良影响。这种毒性包括一系列异质性疾病,从相对良性的心律失常到潜在致命的病症,如心肌缺血/梗死和心肌病。在某些情况下,这些毒性作用的发病机制已经阐明,而在其他情况下,确切病因仍然未知。我们在此回顾据报道与抗肿瘤药物相关的各种心脏毒性综合征,并讨论其假定机制和治疗方法。