首页> 外文期刊>Advances in therapy. >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
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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

机译:CFTR校正器和增强剂组合治疗患者F508DEL-CFTR纯合突变患者的疗效和安全性:系统评价和荟萃分析

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IntroductionCystic 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.MethodsThe 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.ResultsFive 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 FEV1 (ppFEV(1)) (MD 2.38, 1.62-3.15, P0.00001), 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).ConclusionsCFTR 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.
机译:引入纤维化(CF)是一种渐进的遗传疾病,导致持续的肺部感染,并限制随着时间的推移呼吸的能力。囊性纤维化跨膜电导调节剂(CFTR)校正器和电压器的组合通过降低CF中的汗液氯化物浓度为F508DEL-CFTR纯合突变,但它在肺功能,营养状况,临床评分和安全性中仍存在争议。作者对随机对照试验(RCT)进行了系统评价和荟萃分析,以评估CF对F508DEL-CFTR纯合突变的CF肺功能,营养状况,临床评分和安全性的疗效和安全性。搜查了科学网,Cochrane中央登记术,监控试验,MEDLINE和EMBASE。注册的Prospero号码是CRD42018085875.Resultsfive RCT,包括接受CFTR校正器和高压剂组合治疗的F508del-CFTR纯合突变的总共1637名参与者以及基本治疗的突变。初步分析表明,联合治疗改善了预测的FEV1(PPFEV(1))的百分比(MD 2.38,1.62-3.15,P <0.00001),囊性纤维化问卷调查(CFQ-R)呼吸结构域评分(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)。在二次分析中,联合治疗对参与者的数量没有影响报告不良事件(或0.88,0.58-1.33,p = 0.53),但由于不良事件(或2.71,1.3-5.63, P = 0.008).Conclusionscftr校正器和高压蛋白组合治疗有效提高CF患者肺功能,营养状况和临床评分,患有F508DEL-CFTR纯合突变,具有可接受的安全性。

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