Johns Hopkins University, Towson, MD 21204, USA.
Am J Ther. 2010 Jan-Feb;17(1):68-74. doi: 10.1097/MJT.0b013e318199d6b7.
Thrombocytopenia, a decreased platelet count, is a common clinical feature that may be caused by decreased platelet production or accelerated platelet removal. Accelerated platelet removal may result from various immunologic mechanisms, excessive consumption, or sequestration of platelets in the spleen. Thrombocytopenia can range from a transient, isolated finding to a severe, life-threatening condition. Eltrombopag (SB497115) is a novel, orally bioavailable, small-molecule thrombopoetin receptor agonist that induces differentiation and proliferation of megakaryocytes. Preclinical testing on healthy volunteers shows high drug bioavailability and efficacy in raising platelet counts. The 10-day treatment with eltrombopag increased platelet count up to 1.5 times. The drug is usually tolerated well and serious adverse events and discontinuation are rare. There is an unmet need for this agent, and probably eltrombopag is indeed the "drug of choice" for some limited categories of patients; however, its long-term safety profile is unknown. To evaluate the potential drug development, careful analysis of thrombocytopenia morbidity and prevalence of the applicable for treatment with eltrombopag clinical scenarios is highly warranted. Lack of vascular outcome data with regard to potential excessive activity of these next-generation novel platelets may result in increased thrombotic risks and cause worsened cardiovascular and stroke outcomes may be the major obstacle to the success of this promising agent.
血小板减少症,即血小板计数降低,是一种常见的临床特征,可能由血小板生成减少或血小板清除加速引起。血小板清除加速可能由各种免疫机制、过度消耗或血小板在脾脏中的隔离引起。血小板减少症的范围可以从短暂的孤立性发现到严重的危及生命的状况。艾曲波帕(SB497115)是一种新型、口服生物利用度的小分子血小板生成素受体激动剂,可诱导巨核细胞的分化和增殖。在健康志愿者中的临床前测试表明,该药具有较高的药物生物利用度和升高血小板计数的疗效。艾曲波帕的 10 天治疗可将血小板计数提高至 1.5 倍。该药通常耐受性良好,严重不良事件和停药均少见。该药具有未满足的需求,对于某些有限类别的患者,可能确实是“首选药物”;但是,其长期安全性未知。为了评估该药物的潜在开发,对适用于艾曲波帕治疗的血小板减少症发病和流行率进行仔细分析是非常必要的。由于这些新一代新型血小板可能存在过度活跃,而缺乏血管结局数据,可能会导致血栓形成风险增加,从而导致心血管和中风结局恶化,这可能是该有前途的药物成功的主要障碍。