Medizinische Klinik mit Schwerpunkt Hämatologie, Onkologie und Tumorbiologie, Ambulantes Gesundheitszentrum, Charité Universitätsmedizin Berlin - Campus Virchow Klinikum, Berlin, Germany ; Deutsche Gesellschaft für Hämatologie und Medizinische Onkologie, Berlin, Germany.
Transfus Med Hemother. 2013 Oct;40(5):319-25. doi: 10.1159/000355006. Epub 2013 Sep 11.
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.
血小板减少症是一种常见的血液系统疾病。刺激血小板生成可能会降低血小板减少症引起出血的风险,预防严重的血小板减少症,并减少血小板输注的需求。关键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生成。TPO 在肝脏中合成。TPO 从实验室开发成为一种治疗工具的过程非常具有挑战性。第一代促血小板生成因子的临床试验于 2001 年停止。目前,第二代促血小板生成剂仅被批准为慢性免疫性血小板减少症三线治疗的孤儿药。更需要的人群是骨髓增生异常综合征患者、化疗引起的血小板减少症患者、其他形式的遗传性和获得性骨髓衰竭患者、丙型肝炎感染患者或肝硬化患者。