尼罗替尼
帕纳替尼
医学
达沙替尼
伊马替尼
不利影响
髓系白血病
甲磺酸伊马替尼
内科学
酪氨酸激酶
心脏病学
肿瘤科
受体
作者
Peter Valent,Emir Hadzijusufovic,Gerit‐Holger Schernthaner,Dominik Wolf,Delphine Réa,Philipp le Coutre
出处
期刊:Blood
[American Society of Hematology]
日期:2015-02-05
卷期号:125 (6): 901-906
被引量:249
标识
DOI:10.1182/blood-2014-09-594432
摘要
Abstract Vascular safety is an emerging issue in patients with chronic myeloid leukemia (CML) treated with tyrosine kinase inhibitors (TKIs). Whereas imatinib exhibits a well-documented and favorable long-term safety profile without obvious accumulation of vascular events, several types of vascular adverse events (VAEs) have been described in patients receiving second- or third-generation BCR/ABL1 TKIs. Such VAEs include pulmonary hypertension in patients treated with dasatinib, peripheral arterial occlusive disease and other arterial disorders in patients receiving nilotinib, and venous and arterial vascular occlusive events during ponatinib. Although each TKI interacts with a unique profile of molecular targets and has been associated with a unique pattern of adverse events, the mechanisms of drug-induced vasculopathy are not well understood. Here, recent data and concepts around VAEs in TKI-treated patients with CML are discussed, with special reference to potential mechanisms, event management, and strategies aimed at avoiding occurrence of such events in long-term treated patients.
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