Butler Liesl A, Forsyth Cecily, Harrison Claire, Perkins Andrew C
Monash University Melbourne Victoria Australia.
Alfred Health Melbourne Victoria Australia.
EJHaem. 2025 Mar 21;6(2):e70007. doi: 10.1002/jha2.70007. eCollection 2025 Apr.
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.
In this case-based review, we use seven informative common clinical scenarios to discuss appropriate investigation and management of cytopenias and infection issues.
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.
鲁索替尼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。目前在全球范围内,它被用作晚期疾病(中级2和高危)的一线治疗药物,对真性红细胞增多症(PV)和原发性血小板增多症(ET)有效,但在许多国家未被批准用于该适应症。鲁索替尼在症状控制、脾脏缩小和生存期延长方面已被证明具有益处;然而,它很少能使等位基因负担大幅降低,也无法治愈疾病。此外,经常会出现不良反应和给药问题,需要仔细管理以优化其治疗效果。
在本基于病例的综述中,我们使用七个信息丰富的常见临床场景来讨论血细胞减少症和感染问题的适当检查与管理。
我们根据使用鲁索替尼和其他JAK抑制剂治疗骨髓纤维化15年的经验提出建议。我们讨论了何时应考虑进行异基因造血干细胞移植(AHSCT),以及当AHSCT不可行时一些目前可用的替代JAK抑制剂和试验选择。