Hematology Project Foundation, Affiliated to the Department of Haematology, S. Bortolo Hospital, Vicenza, Italy.
Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
J Thromb Haemost. 2018 Sep;16(9):1700-1710. doi: 10.1111/jth.14217. Epub 2018 Jul 27.
Hereditary thrombocytopenias (HTPs) constitute a heterogeneous group of diseases characterized by a reduction in platelet count and a potential bleeding risk. As a result of advances in diagnostic methods, HTPs are increasingly being identified, and appear to be less rare than previously thought. Most HTPs do not have effective treatments, except for platelet transfusion when bleeding occurs and in preparation for procedures associated with a risk of bleeding. Preliminary clinical evidence suggests that thrombopoietin receptor agonists (TPO-RAs) with an established use in the treatment of certain acquired thrombocytopenias are well tolerated and provide clinical benefits in patients with some forms of HTP. These drugs may therefore be considered for the treatment of HTPs in clinical practice. However, caution and close monitoring are recommended, owing to the absence of long-term safety data and the potential risks posed by prolonged bone marrow stimulation in certain HTPs. In this review, we summarize the available clinical data on TPO-RAs in the treatment of HTPs, and discuss their use in patients with these disorders. We believe that TPO-RAs will play a major role in the treatment of HTPs, particularly myosin heavy chain 9-related disease, Wiskott-Aldrich syndrome, X-linked thrombocytopenia, and thrombocytopenia caused by THPO mutations.
遗传性血小板减少症(HTPs)是一组异质性疾病,其特征为血小板计数减少和潜在的出血风险。由于诊断方法的进步,HTPs 的检出率越来越高,而且似乎比以前认为的要少见。大多数 HTPs 没有有效的治疗方法,除了出血时输注血小板和在与出血风险相关的操作前准备时输注血小板。初步临床证据表明,在治疗某些获得性血小板减少症方面具有既定用途的血小板生成素受体激动剂(TPO-RAs)在某些 HTP 患者中耐受性良好,并提供临床获益。因此,这些药物可能被考虑用于临床实践中的 HTP 治疗。然而,鉴于缺乏长期安全性数据以及某些 HTP 中长时间骨髓刺激带来的潜在风险,建议谨慎并密切监测。在这篇综述中,我们总结了 TPO-RAs 在治疗 HTPs 方面的现有临床数据,并讨论了其在这些疾病患者中的应用。我们认为 TPO-RAs 将在 HTPs 的治疗中发挥重要作用,特别是肌球蛋白重链 9 相关疾病、Wiskott-Aldrich 综合征、X 连锁血小板减少症和 THPO 突变引起的血小板减少症。