Janus激酶抑制剂治疗骨髓增殖性肿瘤:心血管安全性荟萃分析

IF 1.2 EJHaem Pub Date : 2025-02-12 DOI:10.1002/jha2.70000
Roberta Dunn, Edouard Long, Laura Li Gagnon, Claire Harrison, Yunfan Yang, Jennifer O'Sullivan
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引用次数: 0

摘要

背景Janus激酶抑制剂(JAKis)是骨髓增生性肿瘤(mpn)治疗中不可或缺的一个方面。JAKis的部分临床益处可能是由于血栓形成的减少,血栓形成是mpn的潜在威胁生命的并发症。然而,有证据表明JAKis继发的心血管不良反应。我们对JAKis治疗mpn的心血管安全性进行了首次荟萃分析。方法本研究按照系统评价和荟萃分析首选报告项目(PRISMA)进行。系统检索比较JAKi治疗与对照组的研究。报告高血压、主要不良心血管事件(MACE)和血栓栓塞事件的研究被纳入荟萃分析,使用随机效应模型进行初级分析,固定效应模型用于进行任何亚组分析。结果23篇文献符合纳入标准,包括9项临床试验和1项回顾性分析。结果共纳入2198例患者(JAKi n = 1145, Control n = 1053)。在报告血栓栓塞事件的研究中(n = 9),合并分析显示JAKi组血栓栓塞事件发生率显著降低(发病率比(IRR): 0.52, 95% CI: 0.28-0.98, p = 0.04)。这主要是由鲁索利替尼治疗骨髓纤维化(MF)和真性红细胞增多症(PV)的研究推动的,当对这些试验进行亚组分析(n = 7)时,发现JAKi治疗的血栓栓塞事件减少更为显著(IRR: 0.41, 95%CI: 0.26-0.64, p <;0.001)。JAKi组与对照组在MACE和高血压方面无显著差异。本荟萃分析表明,JAKi治疗MPN与血栓栓塞事件风险降低相关;主要是由鲁索利替尼在PV和MF中的研究推动的。需要进一步的前瞻性临床试验来证实这些发现,并确定其他JAKis和其他类型mpn的心血管特征。
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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Treatment of Myeloproliferative Neoplasms With Janus Kinase Inhibitors: A Meta-Analysis of Cardiovascular Safety

Background

Janus kinase inhibitors (JAKis) are an integral aspect of the management of myeloproliferative neoplasms (MPNs). Part of the clinical benefit derived from JAKis may be due to reductions in thrombosis, a potentially life-threatening complication of MPNs. However, evidence has emerged of adverse cardiovascular effects secondary to JAKis. We conducted a first-of-a-kind meta-analysis of the cardiovascular safety of JAKis in the treatment of MPNs.

Methods

This study was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA). Systematic searches for studies comparing JAKi treatment to a control group were conducted. Studies reporting hypertension, major adverse cardiovascular events (MACE) and thromboembolic events were included in a meta-analysis using a random-effects model for the primary analysis, and fixed-effects model for any subgroup analyses performed.

Results

A total of 23 publications, consisting of nine clinical trials and one retrospective analysis, met the inclusion criteria. This resulted in a pooled population of 2198 patients (JAKi n = 1145, Control n = 1053). In studies reporting thromboembolic events (n = 9), pooled analysis revealed a significantly lower rate of thromboembolic events in the JAKi group (incidence rate ratio (IRR): 0.52, 95% CI: 0.28–0.98, p = 0.04). This was primarily driven by ruxolitinib studies in myelofibrosis (MF) and polycythemia vera (PV) as when a subgroup analysis of these trials was performed (n = 7), an even more significant reduction in thromboembolic events with JAKi treatment was found (IRR: 0.41, 95%CI: 0.26–0.64, p < 0.001). There was no significant difference in MACE or hypertension between JAKi and control groups.

Conclusion

This meta-analysis suggests that JAKi treatment of MPN was associated with a reduced risk of thromboembolic events; primarily driven by studies of ruxolitinib in PV and MF. Further prospective clinical trials are warranted to confirm these findings and characterise the cardiovascular profile of other JAKis and other types of MPNs.

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