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Drugs. 2021 Jun;81(8):935-943. doi: 10.1007/s40265-021-01524-y. Epub 2021 May 10.
Fostamatinib (Tavalisse; Tavlesse) is the first spleen tyrosine kinase (Syk) inhibitor approved for the treatment of chronic immune thrombocytopenia (ITP) in adult patients who have had an insufficient response to previous treatment. By inhibiting Syk activation in macrophages, fostamatinib blocks autoantibody-mediated platelet phagocytosis. In the placebo-controlled phase III FIT1 and FIT2 trials, 24 weeks of oral fostamatinib therapy increased platelet count in previously treated adults with ITP. A significantly higher proportion of patients achieved stable response with fostamatinib than with placebo in FIT1, but not in FIT2; however, pooled analyses of the two studies showed that fostamatinib produced significantly higher stable and overall response rates than placebo. Interim findings from the ongoing FIT3 open-label extension study suggested that the efficacy of fostamatinib was maintained with long-term treatment (up to 62 months; median duration 6 months), including in patients receiving fostamatinib as second- or later-line treatment. Fostamatinib had a generally manageable tolerability profile in all three FIT studies, with no serious safety risks. Fostamatinib therefore provides an alternative treatment option for chronic ITP in adult patients with an insufficient response to previous treatment.
福他替尼(Tavalisse;Tavlesse)是首个获批用于治疗对既往治疗反应不足的成人慢性免疫性血小板减少症(ITP)的脾酪氨酸激酶(Syk)抑制剂。通过抑制巨噬细胞中 Syk 的激活,福他替尼阻断了自身抗体介导的血小板吞噬作用。在安慰剂对照的 III 期 FIT1 和 FIT2 试验中,24 周的口服福他替尼治疗可增加既往治疗过的 ITP 成人的血小板计数。与安慰剂相比,FIT1 中接受福他替尼治疗的患者达到稳定应答的比例显著更高,但在 FIT2 中则不然;然而,两项研究的汇总分析显示,福他替尼产生的稳定应答和总体应答率显著高于安慰剂。正在进行的开放标签扩展研究 FIT3 的中期结果表明,福他替尼的疗效在长期治疗(最长 62 个月;中位治疗时间为 6 个月)中得以维持,包括接受福他替尼作为二线或更后线治疗的患者。在所有三项 FIT 研究中,福他替尼的耐受性总体上良好,无严重安全风险。因此,福他替尼为对既往治疗反应不足的成人慢性 ITP 提供了一种替代治疗选择。