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Clinical indications for thrombopoietin and thrombopoietin-receptor agonists

机译:血小板生成素和血小板生成素受体激动剂的临床适应症

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摘要

Thrombocytopenia is a common hematologic disorder. Stimulation of thrombopoiesis may reduce the risk for thrombocytopenia-induced bleeding, prevent severe thrombocytopenia, and reduce the need for platelet transfusion. The key cytokine is thrombopoietin (TPO). It regulates proliferation and maturation of megakaryocytes as well as platelet production. TPO is synthesized in the liver. Development of TPO from the laboratory into a therapeutic tool has turned out to be an unexpected challenge. Clinical trials on first-generation thrombopoietic growth factors were stopped in 2001. At present, second-generation thrombopoiesis-stimulating agents have only been approved as orphan drugs for third-line therapy of patients with chronic immune thrombocytopenia. Larger groups in need are patients with myelodysplastic syndrome, chemotherapy-induced thrombocytopenia, other forms of hereditary and acquired bone marrow failure, hepatitis C infections, or liver cirrhosis.
机译:血小板减少症是常见的血液病。刺激血小板生成可以减少血小板减少引起的出血的风险,防止严重的血小板减少,并减少血小板输注的需要。关键的细胞因子是血小板生成素(TPO)。它调节巨核细胞的增殖和成熟以及血小板的产生。 TPO在肝脏中合成。将TPO从实验室发展为治疗工具已成为意料之外的挑战。第一代血小板生成生长因子的临床试验于2001年停止。目前,第二代血小板生成刺激剂仅被批准作为孤儿药物用于慢性免疫性血小板减少症患者的三线治疗。需要治疗的人群较大,有骨髓增生异常综合症,化疗引起的血小板减少,其他形式的遗传性和获得性骨髓衰竭,丙型肝炎感染或肝硬化。

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