Hematology and Oncology Center, Hospital Israelita Albert Einstein, Avenida Albert Einstein, 627/701, Building A, Sao Paulo, SP 05651-901, Brazil.
Hematol Oncol Clin North Am. 2012 Oct;26(5):1083-99. doi: 10.1016/j.hoc.2012.07.008. Epub 2012 Aug 21.
The development of JAK2 inhibitors followed the discovery of activating mutation of JAK2 (JAK2V617F) in patients with classic Philadelphia-negative myeloproliferative neoplasms (Ph-negative MPN). It is now known that mutations activating the JAK-STAT pathway are ubiquitous in Ph-negative MPN, and that the deregulated JAK-STAT pathway plays a central role in the pathogenesis of these disorders. JAK2 inhibitors thus are effective in patients both with and without the JAK2V617F mutation. This article reviews the rationale for using JAK2 inhibitors in Ph-negative MPN, and the results of more recent clinical trials with these drugs.
JAK2 抑制剂的发展是在经典费城染色体阴性骨髓增殖性肿瘤(Ph 阴性 MPN)患者中发现 JAK2 激活突变(JAK2V617F)之后出现的。现在已知,激活 JAK-STAT 通路的突变在 Ph 阴性 MPN 中普遍存在,而失调的 JAK-STAT 通路在这些疾病的发病机制中起着核心作用。因此,JAK2 抑制剂对有和没有 JAK2V617F 突变的患者都有效。本文综述了在 Ph 阴性 MPN 中使用 JAK2 抑制剂的原理,以及这些药物最近临床试验的结果。