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新发现的前沿性囊性纤维化三联组合疗法:一项系统评价

Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review.

作者信息

Dawood Sarah N, Rabih Ahmad M, Niaj Ahmad, Raman Aishwarya, Uprety Manish, Calero Maria Jose, Villanueva Maria Resah B, Joshaghani Narges, Villa Nicole, Badla Omar, Goit Raman, Saddik Samia E, Mohammed Lubna

机构信息

Pediatrics, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

出版信息

Cureus. 2022 Sep 20;14(9):e29359. doi: 10.7759/cureus.29359. eCollection 2022 Sep.

Abstract

A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacaftor-ivacaftor (Trikafta) has been recently discovered. Its approval by the Food and Drug Administration (FDA) in 2019 has expanded the target therapy group to individuals aged twelve and up with at least one Phe508del (phenylalanine 508 deletion) mutation in the CFTR gene. This systematic review aims to assess this combination therapy's safety and efficacy. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines, an in-depth search was performed. The search was done by utilizing databases such as PubMed Central (PMC), Google Scholar, and Science Direct for articles related to this topic. Studies published in the last five years in the English language were chosen preliminarily. Further eligibility criteria and quality assessment tools were employed to assess the risk of bias and finalize ten articles to be used in this review. The chosen articles constituted four randomized control trials (RCTs), four systematic reviews, and two narrative reviews. The last date for data collection was April 24, 2022. Based on the findings of this review, we concluded that by combining three CFTR modulators, this therapy had outperformed all the currently available medications in terms of improving pulmonary function, reducing exacerbations, and enhancing the quality of life of CF patients. In clinical trials, headache and rash were the most common side effects, and laboratory testing to assess liver function is suggested. Long-term safety and effectiveness must be confirmed by the continued review of real-life patient data. Studies done on triple therapy thus far have been promising. Unfortunately, a small proportion of the CF population remains ineligible for any form of CFTR modulator therapy owing to their type of genetic mutation, and this provides ground for further research in this field.

摘要

最近发现了一种用于调节囊性纤维化(CF)跨膜传导调节因子(CFTR)基因的三联疗法,即依列卡福妥-替扎卡福妥-依伐卡托(Trikafta)。2019年美国食品药品监督管理局(FDA)对其的批准,将靶向治疗群体扩大到了年龄在12岁及以上、CFTR基因中至少有一个Phe508del(苯丙氨酸508缺失)突变的个体。本系统评价旨在评估这种联合疗法的安全性和有效性。按照系统评价和Meta分析的首选报告项目(PRISMA)2020指南,进行了深入检索。检索通过利用诸如PubMed Central(PMC)、谷歌学术和科学Direct等数据库来查找与该主题相关的文章。初步选择了过去五年以英文发表的研究。采用进一步的纳入标准和质量评估工具来评估偏倚风险,并最终确定十篇文章用于本评价。所选文章包括四项随机对照试验(RCT)、四项系统评价和两项叙述性评价。数据收集的截止日期为2022年4月24日。基于本评价的结果,我们得出结论,通过联合三种CFTR调节剂,这种疗法在改善肺功能、减少病情加重以及提高CF患者的生活质量方面优于所有目前可用的药物。在临床试验中,头痛和皮疹是最常见的副作用,建议进行评估肝功能的实验室检查。长期安全性和有效性必须通过对真实患者数据的持续评价来确认。迄今为止对三联疗法的研究很有前景。不幸的是,由于基因突变类型,一小部分CF患者仍然没有资格接受任何形式的CFTR调节剂治疗,这为该领域的进一步研究提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d23/9583755/6d3cda3416d5/cureus-0014-00000029359-i01.jpg

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