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Eltrombopag: a review of its use in the treatment of thrombocytopenia in patients with chronic hepatitis C.

机译:Eltrombopag:其在慢性丙型肝炎患者血小板减少症治疗中的应用综述。

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摘要

Eltrombopag (Revolade(?); Promacta(?)) is an orally bioavailable, small-molecule, thrombopoietin receptor agonist that selectively binds to thrombopoietin receptors on megakaryocyte precursors and megakaryocytes leading to increased platelet production. It is approved in a number of countries for the treatment of thrombocytopenia, including adult patients with chronic hepatitis C virus (HCV) infection to allow for the initiation and maintenance of peginterferon-based therapy, which is the focus of this review. In two, well-designed, randomized controlled trials in adults with chronic HCV infection and thrombocytopenia (ENABLE-1 and ENABLE-2), eltrombopag increased platelet counts to sufficient levels to allow for the initiation of peginterferon-based antiviral therapy in 95 % of patients whose baseline platelet counts would have made them ineligible or marginal candidates for peginterferon therapy. Moreover, a significantly higher proportion of eltrombopag recipients than placebo recipients achieved a sustained virological response (primary endpoint) 24 weeks after the completion of antiviral therapy. Of note, the additional benefit over placebo was relatively small (<10 %). Compared with placebo, eltrombopag was associated with fewer patients discontinuing antiviral therapy early and a numerically greater proportion of patients not requiring antiviral dose reduction. Oral eltrombopag had an acceptable tolerability profile; however, there is an increased risk of adverse events, including potentially fatal hepatic decompensation and thromboembolic events. Eltrombopag provides a new treatment option for thrombocytopenia in patients with chronic HCV infection to allow for optimal antiviral therapy.
机译:Eltrombopag(Revolade(?); Promacta(?))是一种口服生物利用的小分子血小板生成素受体激动剂,可选择性地与巨核细胞前体和巨核细胞上的血小板生成素受体结合,从而导致血小板生成增加。它已在许多国家/地区被批准用于治疗血小板减少症,包括患有慢性丙型肝炎病毒(HCV)感染的成年患者,以便开始和维持基于聚乙二醇干扰素的治疗,这是本综述的重点。在两项针对成人慢性HCV感染和血小板减少症(ENABLE-1和ENABLE-2)的精心设计的随机对照试验中,eltrombopag将血小板计数增加至足够水平,以允许在95%的患者中启动基于聚乙二醇干扰素的抗病毒治疗基线血小板计数使他们不适合或处于边缘人群接受聚乙二醇干扰素治疗的患者。此外,在完成抗病毒治疗后24周内,Eltrombopag接受者的比例显着高于安慰剂接受者,达到了持续的病毒学应答(主要终点)。值得注意的是,与安慰剂相比,其他益处相对较小(<10%)。与安慰剂相比,eltrombopag与较少的患者早期中止抗病毒治疗相关,并且不需要抗病毒药物减量的患者比例更高。口服Eltrombopag具有可接受的耐受性。但是,不良事件的风险增加,包括潜在的致命性肝失代偿和血栓栓塞事件。 Eltrombopag为慢性HCV感染患者的血小板减少症提供了新的治疗选择,以实现最佳的抗病毒治疗。

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