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本文引用的文献

1
Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele.依伐卡托与泰比卡托和艾克卡托三联复方药物治疗携带单个 F508del 突变的囊性纤维化
N Engl J Med. 2019 Nov 7;381(19):1809-1819. doi: 10.1056/NEJMoa1908639. Epub 2019 Oct 31.
2
Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial.在纯合子 F508del 突变的囊性纤维化患者中,elexacaftor 加 tezacaftor 加 ivacaftor 联合治疗方案的疗效和安全性:一项双盲、随机、3 期临床试验。
Lancet. 2019 Nov 23;394(10212):1940-1948. doi: 10.1016/S0140-6736(19)32597-8. Epub 2019 Oct 31.
3
Cystic fibrosis transmembrane conductance regulator modulators: precision medicine in cystic fibrosis.囊性纤维化跨膜电导调节因子调节剂:囊性纤维化的精准医学。
Curr Opin Pediatr. 2018 Jun;30(3):372-377. doi: 10.1097/MOP.0000000000000627.
4
Cystic Fibrosis Foundation Pulmonary Guidelines. Use of Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy in Patients with Cystic Fibrosis.囊性纤维化基金会肺部指南。囊性纤维化跨膜电导调节剂治疗在囊性纤维化患者中的应用。
Ann Am Thorac Soc. 2018 Mar;15(3):271-280. doi: 10.1513/AnnalsATS.201707-539OT.
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Cystic fibrosis.囊性纤维化。
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依列卡福妥-替扎卡福妥-依伐卡托:首个三联组合型囊性纤维化跨膜传导调节因子调控疗法

Elexacaftor-Tezacaftor-Ivacaftor: The First Triple-Combination Cystic Fibrosis Transmembrane Conductance Regulator Modulating Therapy.

作者信息

Ridley Kaden, Condren Michelle

出版信息

J Pediatr Pharmacol Ther. 2020;25(3):192-197. doi: 10.5863/1551-6776-25.3.192.

DOI:10.5863/1551-6776-25.3.192
PMID:32265602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7134581/
Abstract

Elexacaftor-tezacaftor-ivacaftor is a newly approved triple-combination cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapy that contains 2 correctors and a potentiator of the CFTR channel. Its labeled indication for use is for persons 12 years of age and older with at least 1 F508del mutation for the gene. This drug combination provides potential therapy to many patients who had previously been excluded from CFTR modulation therapy due to the nature of their genetic mutations. The efficacy demonstrated in clinical trials surpasses the currently available therapies related to lung function, quality of life, sweat chloride reduction, and reducing exacerbations. The most common adverse events seen in clinical trials included rash and headache, and laboratory monitoring is recommended to evaluate liver function. Continued evaluation of patient data is needed to confirm its long-term safety and efficacy. Elexacaftor-tezacaftor-ivacaftor is a monumental and encouraging therapy for cystic fibrosis; however, approximately 10% of the CF population are not candidates for this or any other CFTR modulation therapy.

摘要

依列卡福妥-替扎卡福妥-依伐卡福妥是一种新获批的三联组合疗法,用于调节囊性纤维化跨膜传导调节因子(CFTR),它包含2种CFTR通道校正剂和1种增效剂。其获批的适用人群为年龄在12岁及以上、至少携带1个该基因F508del突变的患者。这种药物组合为许多此前因基因突变类型而被排除在CFTR调节疗法之外的患者提供了潜在治疗方案。临床试验中所展示的疗效在肺功能、生活质量、汗液氯化物减少以及减少病情加重等方面超过了目前可用的疗法。临床试验中最常见的不良事件包括皮疹和头痛,建议进行实验室监测以评估肝功能。需要持续评估患者数据以确认其长期安全性和疗效。依列卡福妥-替扎卡福妥-依伐卡福妥对于囊性纤维化而言是一种具有里程碑意义且令人鼓舞的疗法;然而,约10%的囊性纤维化患者不适合这种或任何其他CFTR调节疗法。