Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy

Zhenshu Xu, S. Cang, Ting Yang, Delong Liu
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引用次数: 42

Abstract

Emerging evidence suggests that the three tyrosine kinase inhibitors currently approved for the treatment of patients with chronic myelogenous leukemia (CML) – imatinib, dasatinib, and nilotinib – have potential cardiotoxic effects. The mechanisms behind these events, and the relations between them, are largely unclear. For example, relative to dasatinib and nilotinib, severe congestive heart failure and left ventricular dysfunction are rare but prominent with imatinib treatment, particularly in patients receiving higher doses (>600 mg/day). In comparison with imatinib, prolongation of the QT interval is relatively common in patients treated with either dasatinib or nilotinib. In contrast to nilotinib, pericardial effusions are observed with both imatinib and dasatinib. It is suggested that these data, an evaluation of cardiac status, use of concomitant medications, and potential risk factors should be considered in the management of CML.
慢性粒细胞白血病治疗中酪氨酸激酶抑制剂的心脏毒性
新出现的证据表明,目前批准用于治疗慢性髓性白血病(CML)患者的三种酪氨酸激酶抑制剂——伊马替尼、达沙替尼和尼洛替尼——具有潜在的心脏毒性作用。这些事件背后的机制以及它们之间的关系在很大程度上尚不清楚。例如,相对于达沙替尼和尼洛替尼,严重的充血性心力衰竭和左心室功能障碍是罕见的,但伊马替尼治疗突出,特别是在接受更高剂量(> 600mg /天)的患者中。与伊马替尼相比,在接受达沙替尼或尼洛替尼治疗的患者中,QT间期延长相对常见。与尼洛替尼相反,伊马替尼和达沙替尼均可观察到心包积液。建议在CML的治疗中应考虑这些数据、心脏状态的评估、伴随药物的使用和潜在的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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