Unit of Clinical Epidemiology and Center for the Study of Myelofibrosis, IRCCS Policlinico S. Matteo Foundation, Viale Golgi 19, 27100 Pavia, Italy.
Expert Rev Hematol. 2012 Jun;5(3):313-24. doi: 10.1586/ehm.12.17.
Conventional drugs for myelofibrosis are driven by clinical needs, primarily anemia and splenomegaly. With these therapies, stem cell transplantation remains the only potentially curative approach. The discovery that mutations affecting JAK2 or MPL lead to activation of the intracellular JAK-STAT signaling pathway, and that other mutations (TET2, EZH2, ASXL1, IDH1 and IDH2) interfere with the normal machinery of epigenetics, has prompted to the development of therapies targeted at controling the major disease mechanisms. JAK2 ATP competitive inhibitors (ruxolitinib, lestaurtinib, SAR302503, SB1518 and CYT387) or drugs that indirectly inhibit the JAK-STAT pathway (everolimus) have documented major effects on splenomegaly and its constitutional symptoms. Epigenetic drugs (demethylating agents and histone deacetylase inhibitors) have displayed only minor effects on the disease symptoms. Relenting disease progression remains an unmet clinical need.
针对骨髓纤维化的传统药物主要是基于临床需求,即贫血和脾肿大。这些疗法中,干细胞移植仍然是唯一潜在的治愈方法。已经发现,影响 JAK2 或 MPL 的突变会导致细胞内 JAK-STAT 信号通路的激活,而其他突变(TET2、EZH2、ASXL1、IDH1 和 IDH2)会干扰正常的表观遗传机制,这促使人们开发靶向控制主要疾病机制的治疗方法。JAK2 ATP 竞争性抑制剂(ruxolitinib、lestaurtinib、SAR302503、SB1518 和 CYT387)或间接抑制 JAK-STAT 通路的药物(everolimus)已被证明对脾肿大及其全身症状有显著影响。表观遗传药物(去甲基化剂和组蛋白去乙酰化酶抑制剂)对疾病症状仅有轻微影响。缓解疾病进展仍然是一个未满足的临床需求。