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G551D 突变型囊性纤维化患者中伊伐卡托停药综合征。

Ivacaftor withdrawal syndrome in cystic fibrosis patients with the G551D mutation.

机构信息

Division of Pulmonary & Critical Care Medicine, Division of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, United States.

Division of Pulmonary & Critical Care Medicine, Division of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, United States.

出版信息

J Cyst Fibros. 2018 Mar;17(2):e13-e16. doi: 10.1016/j.jcf.2017.09.006. Epub 2017 Oct 24.

Abstract

Ivacaftor use can lead to dramatic health improvements in cystic fibrosis (CF) patients with gating mutations. Here, we report five instances of dramatic clinical decline following withdrawal of ivacaftor in three individuals with the G551D-CFTR mutation. In each case, the patient's lung function and symptoms rapidly deteriorated after cessation of treatment. Awareness of this phenomenon should inform both clinical practices as well as the design of future clinical trials of highly active CFTR modulators.

摘要

依伐卡托的使用可显著改善具有门控突变的囊性纤维化(CF)患者的健康状况。在这里,我们报告了三例 G551D-CFTR 突变患者停用依伐卡托后出现显著临床恶化的五个实例。在每种情况下,患者的肺功能和症状在停止治疗后迅速恶化。对这种现象的认识应既能为临床实践提供信息,也能为高活性 CFTR 调节剂的未来临床试验设计提供信息。

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