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CFTR 校正剂和增强剂联合治疗 F508del-CFTR 纯合突变囊性纤维化患者的疗效和安全性:系统评价和荟萃分析。

Efficacy and Safety of CFTR Corrector and Potentiator Combination Therapy in Patients with Cystic Fibrosis for the F508del-CFTR Homozygous Mutation: A Systematic Review and Meta-analysis.

机构信息

Department of Respiratory and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, China.

Department of Respiratory Medicine, Chengdu Second People's Hospital, Chengdu, China.

出版信息

Adv Ther. 2019 Feb;36(2):451-461. doi: 10.1007/s12325-018-0860-4. Epub 2018 Dec 15.

Abstract

INTRODUCTION

Cystic fibrosis (CF) is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. The combination of a cystic fibrosis transmembrane conductance regulator (CFTR) corrector and potentiator has provided a benefit by decreasing sweat chloride concentration in CF for the F508del-CFTR homozygous mutation, but it remains controversial in lung function, nutritional status, clinical score and safety.

METHODS

The authors performed a systematic review and meta-analysis of randomized controlled trials (RCTs) to evaluate the efficacy and safety of combination therapy on lung function, nutritional status, clinical score and safety in CF for the F508del-CFTR homozygous mutation. Web of Science, Cochrane Central Register of Controlled Trials, Medline, and Embase were searched. The registered PROSPERO number was CRD42018085875.

RESULTS

Five RCTs, including a total of 1637 participants with the F508del-CFTR homozygous mutation who accepted CFTR corrector and potentiator combination therapy along with basic treatment were enrolled in this analysis. Primary analysis revealed that combination therapy improved the percent of predicted FEV (ppFEV) (MD 2.38, 1.62-3.15, P < 0.00001), Cystic Fibrosis Questionnaire-Revised (CFQ-R) respiratory domain score (MD 2.59, 0.96-4.22, P = 0.002) and body-mass index (BMI) (MD 0.21, 0.03-0.39, P = 0.02). In the secondary analysis, combination therapy had no impact on the number of participants reporting adverse events (OR 0.88, 0.58-1.33, P = 0.53), but increased the proportion of discontinued treatments due to adverse events (OR 2.71, 1.3-5.63, P = 0.008).

CONCLUSIONS

CFTR corrector and potentiator combination therapy effectively improves lung function, nutritional status and clinical score in CF patients with the F508del-CFTR homozygous mutation, and has an acceptable safety profile.

摘要

简介

囊性纤维化(CF)是一种进行性遗传疾病,会导致肺部持续感染,并随着时间的推移逐渐削弱呼吸能力。囊性纤维化跨膜电导调节因子(CFTR)校正剂和增强剂的联合使用,降低了 F508del-CFTR 纯合突变的 CF 患者的汗液氯化物浓度,这一发现具有重要意义,但在肺功能、营养状况、临床评分和安全性方面仍存在争议。

方法

作者对随机对照试验(RCT)进行了系统回顾和荟萃分析,以评估 CFTR 校正剂和增强剂联合治疗对 F508del-CFTR 纯合突变 CF 患者肺功能、营养状况、临床评分和安全性的疗效和安全性。检索了 Web of Science、Cochrane 中央对照试验注册库、Medline 和 Embase。已注册的 PROSPERO 编号为 CRD42018085875。

结果

共纳入了 5 项 RCT,总计 1637 名接受 CFTR 校正剂和增强剂联合治疗及基础治疗的 F508del-CFTR 纯合突变患者。主要分析结果显示,联合治疗组可改善预测的第 1 秒用力呼气量(FEV1)占预计值的百分比(MD 2.38,1.62-3.15,P<0.00001)、囊性纤维化问卷修订版(CFQ-R)呼吸域评分(MD 2.59,0.96-4.22,P=0.002)和体重指数(BMI)(MD 0.21,0.03-0.39,P=0.02)。在次要分析中,联合治疗组报告不良反应的参与者比例无显著差异(OR 0.88,0.58-1.33,P=0.53),但因不良反应而停止治疗的比例更高(OR 2.71,1.3-5.63,P=0.008)。

结论

CFTR 校正剂和增强剂联合治疗可有效改善 F508del-CFTR 纯合突变 CF 患者的肺功能、营养状况和临床评分,且具有可接受的安全性。

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