[新的二线治疗免疫性血小板减少症]。

Hisashi Kato
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引用次数: 0

摘要

免疫性血小板减少症(ITP)是一种血小板减少性疾病,其中抗血小板抗体加速血小板破坏和损害血小板产生。治疗包括一线类固醇,如果患者对类固醇无反应或不耐受,随后进行二线治疗。血小板生成素受体激动剂、利妥昔单抗和脾切除术是主要的二线治疗方案。然而,Syk抑制剂fostamatinib和FcRn抑制剂efgartigimod这两种有望通过一种新的作用机制改善血小板计数的新药,最近在日本也被列为二线治疗选择。许多新的ITP治疗药物,如BTK抑制剂、BAFF受体抑制剂和抗cd38抗体药物也在开发中。希望这些具有不同疗效的新型治疗方案能够在未来改善ITP的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Novel second-line treatments for immune thrombocytopenia].

Immune thrombocytopenia (ITP) is a thrombocytopenic disorder in which anti-platelet antibodies accelerate platelet destruction and impair platelet production. Treatment consists of first-line steroids, followed by second-line therapy if the patient is unresponsive or intolerant to steroids. Thrombopoietin receptor agonists, rituximab, and splenectomy have been the main second-line options. However, the Syk inhibitor fostamatinib and the FcRn inhibitor efgartigimod, two novel agents that are expected to improve platelet counts through a new mechanism of action, have recently been added as second-line treatment options in Japan as well. Many new therapeutic agents for ITP such as BTK inhibitors, BAFF receptor inhibitors, and anti-CD38 antibody agents are also under development. It is hoped that these novel treatment options with different effects will improve the management of ITP in the future.

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