NEJM:Jakavi(ruxolitinib)治疗急性移植物抗宿主病,优于现有更佳疗法

2020-04-23 Allan MedSci原创

今天发表于《新英格兰医学杂志》的III期REACH2研究表明,与现有最佳药物相比,Jakavi(ruxolitinib)改善了激素抵抗性急性移植物抗宿主病(GvHD)患者的一系列疗效指标。

今天发表于《新英格兰医学杂志》的III期REACH2研究表明,与现有最佳药物相比,Jakavi(ruxolitinib)改善了激素抵抗性急性移植物抗宿主病(GvHD)患者的一系列疗效指标。REACH2是第一个达到主要终点的急性GvHD的III期研究。REACH2试验的详细数据将在8月30日至9月2日在西班牙马德里举行的欧洲血液和骨髓移植学会(EBMT)年度会议上介绍。

相比于现有最佳药物,接受Jakavi治疗的患者在第28天具有更高的总缓解率(ORR)(62%比39%,p<0.001);接受Jakavi治疗的患者在8周时的ORR显著更高(40%比22%,p<0.001)。此外,Jakavi的FFS比现有最佳药物更长(5.0个月比1.0个月)。

该研究的主要领导者说:“急性移植物抗宿主病患者面临着生命威胁和有限的治疗选择,特别是对于激素抵抗性患者。来自REACH2的数据表明,Jakavi优于当前最佳药物。这些证据表明,在这种难以治疗的情况下,靶向JAK途径可以成为一种有效的策略”。

 

原始出处:

https://www.firstwordpharma.com/node/1717840?tsid=4

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    2020-05-05 xuyong535
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    2020-04-25 wincls
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    2020-04-23 旺医

    顶刊就是顶刊,谢谢梅斯带来这么高水平的研究报道,我们科里同事经常看梅斯,分享梅斯上的信息

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Ann Hematol:急性移植物抗宿主病增加骨髓增生异常综合征患者移植相关血栓性微血管病预测模型的风险和准确性

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NEJM:老药新用——西格列汀可降低造血干细胞移植后急性移植物抗宿主病风险

急性移植物抗宿主病(GVHD)是异基因造血干细胞移植(HSCT)后的常见并发症,导致患者不良预后风险增加。 GVHD的标准预防方案,包括钙调神经磷酸酶抑制剂与甲氨蝶呤或西罗莫司。统计发现在HLA匹配的