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骨髓增殖性肿瘤的突破

Breakthroughs in myeloproliferative neoplasms.

作者信息

Santos Fabio P S, Verstovsek Srdan

机构信息

Hematology and Stem Cell Transplantation, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.

出版信息

Hematology. 2012 Apr;17 Suppl 1:S55-8. doi: 10.1179/102453312X13336169155574.

Abstract

The discovery of the JAK2V617F mutation ushered the field of Philadelphia-negative myeloproliferative neoplasms (MPNs) into the era of targeted therapy. Currently, there are several JAK2 inhibitors in clinical trials for patients with MPNs, particularly for patients with myelofibrosis (MF). These drugs act by blocking the proliferation of neoplastic cells by disrupting the JAK2-STAT signaling and by abrogating inflammatory cytokine signaling which is dependent on JAK kinases. Therapy with JAK2 inhibitors can improve splenomegaly and debilitating constitutional symptoms in great majority of MF patients, improving greatly their quality of life. Long-term follow-up will reveal whether these drugs can also prolong survival by better controlling signs and symptoms of the MF. There are other compounds in clinical trials for MPNs, including the new immunomodulatory drug pomalidomide, and inhibitor of mammalian target of Rapamycin everolimus. In this article, we briefly review the latest therapeutic advances in the field of Philadelphia-negative MPNs.

摘要

JAK2V617F 突变的发现,将费城染色体阴性骨髓增殖性肿瘤(MPNs)领域带入了靶向治疗时代。目前,有几种 JAK2 抑制剂正处于针对 MPN 患者的临床试验中,特别是针对骨髓纤维化(MF)患者。这些药物通过破坏 JAK2-STAT 信号传导以及废除依赖 JAK 激酶的炎性细胞因子信号传导来阻断肿瘤细胞的增殖。使用 JAK2 抑制剂进行治疗可改善绝大多数 MF 患者的脾肿大和使人衰弱的全身症状,极大地提高他们的生活质量。长期随访将揭示这些药物是否也能通过更好地控制 MF 的体征和症状来延长生存期。还有其他化合物正处于针对 MPNs 的临床试验中,包括新型免疫调节药物泊马度胺以及雷帕霉素哺乳动物靶点抑制剂依维莫司。在本文中,我们简要回顾费城染色体阴性 MPNs 领域的最新治疗进展。

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