Basood May, Oster Howard S, Mittelman Moshe
Department of Medicine A, Tel Aviv Sourasky Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, ISRAEL.
Mediterr J Hematol Infect Dis. 2018 Jul 1;10(1):e2018046. doi: 10.4084/MJHID.2018.046. eCollection 2018.
The myelodysplastic syndromes (MDS) are a group of clonal bone marrow (BM) stem cell disorders, characterized by ineffective hematopoiesis, peripheral cytopenias, and hematologic cellular dysfunction, as well as potential transformation to acute leukemia. Thrombocytopenia is common in MDS and is associated with bleeding complications, occasionally life-threatening. Low platelet count (PLT), as well declining PLT also serves as a prognostic marker. Understanding thrombopoiesis led to the cloning of thrombopoietin, resulting in the development of platelet stimulating agents, thrombomimetics, romiplostim and eltrombopag. Both agents have been shown to increase PLT, decrease the need for platelet transfusions and reduce the number of bleeding episodes, with a reasonable tolerance. They are already approved for immune thrombocytopenia and thrombocytopenia related to liver disease. Romiplostim and eltrombopag have proven efficacy in lower- and higher-risk MDS with thrombocytopenia, as monotherapy, as well as a part of a combination, either with lenalidomide, and mainly combined with hypomethylating agents. However, safety concerns have been raised: while several trials have been completed with no evidence of disease progression, others have been early terminated due to an increased number of BM blasts and possible leukemic transformation in treated-patients. The jury is still out regarding this safety concern, although recent publications are more encouraging.
骨髓增生异常综合征(MDS)是一组克隆性骨髓干细胞疾病,其特征为造血无效、外周血细胞减少、血液学细胞功能障碍以及有转化为急性白血病的可能性。血小板减少在MDS中很常见,且与出血并发症相关,偶尔会危及生命。低血小板计数(PLT)以及不断下降的PLT也可作为一种预后标志物。对血小板生成的了解促使血小板生成素的克隆,从而推动了血小板刺激剂、血小板生成素模拟物、罗米司亭和艾曲泊帕的研发。这两种药物均已显示可增加PLT、减少血小板输注需求并减少出血事件数量,且耐受性良好。它们已被批准用于免疫性血小板减少症以及与肝病相关的血小板减少症。罗米司亭和艾曲泊帕已被证明在伴有血小板减少症的低危和高危MDS中作为单药治疗有效,也可作为联合治疗的一部分,与来那度胺联合使用,主要是与去甲基化药物联合使用。然而,也有人提出了安全性问题:虽然已经完成了多项试验,没有疾病进展的证据,但其他一些试验由于治疗患者的骨髓原始细胞数量增加和可能的白血病转化而提前终止。尽管最近的出版物更令人鼓舞,但关于这一安全性问题尚无定论。