Geissler K
Klinische Abteilung für Hämatologie und Hämostaseologie, Allgemeines Krankenhaus-Innere Medizin I, Wien, Osterreich.
Wien Klin Wochenschr. 2000 Oct 13;112(19):829-34.
Thrombocytopenia induced by disease and/or chemotherapy is one of the major complications in the treatment of patients with hemato-oncological malignancies. The discovery of Mpl ligand, a hematopoietic growth factor that stimulates megakaryopoiesis and thrombopoiesis lineage-specifically both in vitro and in preclinical models, is an important step in the development of new treatment concepts for patients with thrombocytopenia. Two recombinant forms of Mpl ligand, recombinant human thrombopoietin (rHuTPO) and pegylated recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF), are currently being tested in clinical trials. Development of these thrombopoietins has recently been constrained due to the observation of anti-thrombopoietin antibodies in some patients following thrombopoietin treatment. However, clinical trials performed so far provide significant insight into the therapeutic potential of these molecules. TPO/MGDF stimulates thrombopoiesis in cancer patients before chemotherapy and reduces the duration and sometimes the degree of thrombocytopenia following myelosuppressive chemotherapy. Despite marked thrombocytosis in some of these patients an increased risk for thromboembolic complications was not observed. Although administration of TPO/MGDF has provided some clinical benefit after autologous bone marrow transplantation, such effects have not been found in the settings of peripheral blood stem cell transplantation and aplasiogenic AML chemotherapy. The potential role of Mpl ligand in other indications such as thrombocytopenia in liver disease, plateletpheresis and stem cell expansion remains to be determined. Recent efforts in the development of thrombopoietins focus on the generation of molecules with maintained thrombopoietic activity which are not immunogenic.
疾病和/或化疗引起的血小板减少症是血液肿瘤恶性肿瘤患者治疗中的主要并发症之一。Mpl配体的发现是治疗血小板减少症患者新治疗理念发展中的重要一步,Mpl配体是一种造血生长因子,在体外和临床前模型中均能特异性刺激巨核细胞生成和血小板生成。两种重组形式的Mpl配体,即重组人血小板生成素(rHuTPO)和聚乙二醇化重组人巨核细胞生长和发育因子(PEG-rHuMGDF),目前正在临床试验中进行测试。由于在一些患者接受血小板生成素治疗后观察到抗血小板生成素抗体,这些血小板生成素的开发最近受到了限制。然而,迄今为止进行的临床试验为这些分子的治疗潜力提供了重要的见解。TPO/MGDF在化疗前刺激癌症患者的血小板生成,并缩短骨髓抑制化疗后血小板减少的持续时间,有时还能减轻其程度。尽管其中一些患者出现明显的血小板增多症,但未观察到血栓栓塞并发症风险增加。虽然TPO/MGDF在自体骨髓移植后提供了一些临床益处,但在外周血干细胞移植和再生障碍性AML化疗的情况下尚未发现此类效果。Mpl配体在其他适应症中的潜在作用,如肝病中的血小板减少症、血小板单采和干细胞扩增,仍有待确定。血小板生成素开发的近期努力集中在生成具有维持血小板生成活性且无免疫原性的分子。