原发性血小板增多症/真性红细胞增多症的新治疗策略。

IF 2.3 Q2 HEMATOLOGY Blood Research Pub Date : 2023-04-30 DOI:10.5045/br.2023.2023013
Seug Yun Yoon, Jong-Ho Won
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引用次数: 1

摘要

骨髓增生性肿瘤(mpn)是造血干细胞的克隆性疾病;这些包括真性红细胞增多症(PV)、原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)。mpn是炎症性癌症,其中恶性克隆产生细胞因子,维持炎症驱动在一个自我延续的恶性循环。mpn的病程遵循生物学连续体,即从早期癌症阶段(ET/PV)到晚期骨髓纤维化以及即将发生的白血病转化。mpn相关症状,如疲劳、全身无力和瘙痒,是由炎症细胞因子引起的。炎症因子也会加重MPN患者的血栓形成和出血。直到最近,ET和PV治疗的主要目的是通过预防血栓形成来提高生存率。然而,最近有几种药物被证明有能力改变疾病的进程;大多数患者的症状可望得到缓解。此外,人们对低风险PV和ET患者的积极治疗越来越感兴趣。本文将重点介绍ET/PV治疗策略以及临床开发的新治疗方案。
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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Novel therapeutic strategies for essential thrombocythemia/polycythemia vera.

Myeloproliferative neoplasms (MPNs) are clonal disorders of hematopoietic stem cells; these include polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). MPNs are inflammatory cancers, wherein the malignant clone generates cytokines that sustain the inflammatory drive in a self-perpetuating vicious cycle. The course of MPNs follows a biological continuum, that is, from early cancer stages (ET/PV) to advanced myelofibrosis as well as impending leukemic transformation. MPN-related symptoms, e.g., fatigue, general weakness, and itching, are caused by inflammatory cytokines. Thrombosis and bleeding are also exacerbated by inflammatory cytokines in patients with MPN. Until recently, the primary objective of ET and PV therapy was to increase survival rates by preventing thrombosis. However, several medications have recently demonstrated the ability to modify the course of the disease; symptom relief is expected for most patients. In addition, there is increasing interest in the active treatment of patients at low risk with PV and ET. This review focuses on the ET/PV treatment strategies as well as novel treatment options for clinical development.

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来源期刊
Blood Research
Blood Research HEMATOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
64
期刊最新文献
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