鲁索利替尼治疗骨髓纤维化患者的细胞减少和感染的现实世界管理

EJHaem Pub Date : 2025-03-21 DOI:10.1002/jha2.70007
Liesl A. Butler, Cecily Forsyth, Claire Harrison, Andrew C. Perkins
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引用次数: 0

摘要

Ruxolitinib是首个被批准用于治疗原发性和继发性骨髓纤维化的JAK2抑制剂。目前,它在世界范围内被用作晚期疾病(中-2和高风险)的一线治疗,对真性红细胞增多症(PV)和原发性血小板增多症(ET)有效,但在许多国家没有为这一适应症提供资金。Ruxolitinib在症状控制、脾脏缩小和延长生存期方面已被证明有益处;然而,它很少引起等位基因负担的实质性减少,也从不提供治愈方法。此外,经常会遇到副作用和剂量问题,需要仔细管理以优化其治疗效果。方法和结果在这篇基于病例的综述中,我们使用了7个信息丰富的常见临床场景来讨论细胞减少和感染问题的适当调查和管理。结论:我们基于15年使用ruxolitinib和其他JAK抑制剂治疗骨髓纤维化的经验提出建议。我们讨论了什么时候应该考虑异体造血干细胞移植(AHSCT),以及目前可用的一些替代JAK抑制剂和当AHSCT不可行时的试验选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real World Management of Cytopenias and Infections in Patients With Myelofibrosis Treated With Ruxolitinib

Introduction

Ruxolitinib was the first JAK2 inhibitor approved for the treatment of primary and secondary myelofibrosis. It is currently used worldwide as first-line therapy for advanced disease (intermediate-2 and high-risk) and is effective in polycythaemia vera (PV) and essential thrombocythaemia (ET), but not funded for this indication in many countries. Ruxolitinib has proven benefits with respect to symptom control, reduction in spleen size and prolongation of survival; however, it rarely induces a substantial reduction in allele burden and never provides a cure. Moreover, there are frequently encountered adverse effects and dosing issues that require careful management to optimise its therapeutic benefit.

Methods and Results

In this case-based review, we use seven informative common clinical scenarios to discuss appropriate investigation and management of cytopenias and infection issues.

Conclusions

We make recommendations based on 15 years of experience in using ruxolitinib and other JAK inhibitors for the treatment of myelofibrosis. We discuss when allogeneic haematopoietic stem cell transplantation (AHSCT) should be considered and some of the currently available alternative JAK inhibitors and trial options when AHSCT is not an option.

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