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williamhill asia 带来这么高水平的研究报道,williamhill asia 科里同事经常看williamhill asia ,分享williamhill asia 上的信息

    0

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Itolizumab治疗急性移植物抗宿主病(aGVHD),已取得阳性中期数据

Equillium预计将在2021年上半年报告来自EQUATE试验的所有队列的主要数据。

Blood:替度鲁肽,急性移植物抗宿主病的新选择!

通过GLP-2治疗可以克服由于GVHD引起的L细胞、肠道干细胞和Paneth细胞缺乏;胃肠道内分泌细胞L细胞数量的降低与GVHD患者的预后较差有关。