Recent advances in therapies for primary myelofibrosis.

Faculty reviews Pub Date : 2023-09-26 eCollection Date: 2023-01-01 DOI:10.12703/r/12-23
William Vainchenker, Nasrine Yahmi, Violaine Havelange, Caroline Marty, Isabelle Plo, Stefan N Constantinescu
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Abstract

Primary myelofibrosis (PMF), polycythemia vera (PV) and essential thrombocythemia (ET) form the classical BCR-ABL1-negative myeloproliferative neoplasms (MPNs) that are driven by a constitutive activation of JAK2 signaling. PMF as well as secondary MF (post-ET and post-PV MF) are the most aggressive MPNs. Presently, there is no curative treatment, except allogenic hematopoietic stem cell transplantation. JAK inhibitors, essentially ruxolitinib, are the therapy of reference for intermediate and high-risk MF. However, presently the current JAK inhibitors behave mainly as anti-inflammatory drugs, improving general symptoms and spleen size without major impact on disease progression. A better understanding of the genetics of MF, the biology of its leukemic stem cells (LSCs), the mechanisms of fibrosis and of cytopenia and the role of inflammatory cytokines has led to new approaches with the development of numerous therapeutic agents that target epigenetic regulation, telomerase, apoptosis, cell cycle, cytokines and signaling. Furthermore, the use of a new less toxic form of interferon-α has been revived, as it is presently one of the only molecules that targets the mutated clone. These new approaches have different aims: (a) to provide alternative therapy to JAK inhibition; (b) to correct cytopenia; and (c) to inhibit fibrosis development. However, the main important goal is to find new disease modifier treatments, which will profoundly modify the progression of the disease without major toxicity. Presently the most promising approaches consist of the inhibition of telomerase and the combination of JAK2 inhibitors (ruxolitinib) with either a BCL2/BCL-xL or BET inhibitor. Yet, the most straightforward future approaches can be considered to be the development of and/or selective inhibition of JAK2V617F and the targeting MPL and calreticulin mutants by immunotherapy. It can be expected that the therapy of MF will be significantly improved in the coming years.

Abstract Image

Abstract Image

原发性骨髓纤维化治疗的最新进展。
原发性骨髓纤维化(PMF)、真性红细胞增多症(PV)和原发性血小板增多症(ET)形成了经典的BCR-ABL1阴性骨髓增生性肿瘤(MPNs),其由JAK2信号的组成性激活驱动。PMF和二次MF(ET后和PV后MF)是最具攻击性的MPN。目前,除了同种异体造血干细胞移植外,没有任何治疗方法。JAK抑制剂,本质上是ruxolitinib,是中高风险MF的参考治疗方法。然而,目前的JAK抑制剂主要作为抗炎药,改善一般症状和脾脏大小,对疾病进展没有重大影响。对MF的遗传学、其白血病干细胞(LSCs)的生物学、纤维化和细胞减少的机制以及炎性细胞因子的作用有了更好的了解,开发了许多靶向表观遗传调控、端粒酶、细胞凋亡、细胞周期、细胞因子和信号传导的治疗剂,从而开辟了新的途径。此外,一种毒性较小的新型干扰素-α的使用已经恢复,因为它是目前唯一靶向突变克隆的分子之一。这些新方法有不同的目的:(a)提供JAK抑制的替代疗法;(b) 纠正细胞减少;和(c)抑制纤维化的发展。然而,主要的重要目标是找到新的疾病调节剂治疗方法,这将在没有重大毒性的情况下深刻改变疾病的进展。目前最有前景的方法包括抑制端粒酶和JAK2抑制剂(ruxolitinib)与BCL2/BCL-xL或BET抑制剂的组合。然而,未来最直接的方法可以被认为是通过免疫疗法开发和/或选择性抑制JAK2V617F以及靶向MPL和钙网织蛋白突变体。可以预期,MF的治疗将在未来几年得到显著改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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