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莫达非尼与匹托利生治疗发作性睡病的比较:一种非劣效性荟萃分析方法。

Comparison of modafinil and pitolisant in narcolepsy: a non-inferiority meta-analytical approach.

作者信息

Lehert Philippe, Szoeke Cassandra

机构信息

Faculty of Economics, University of Louvain, Mons, Belgium.

Faculty of Medicine, University of Melbourne, Melbourne, Victoria, Australia.

出版信息

Drugs Context. 2020 Jul 8;9. doi: 10.7573/dic.2020-6-2. eCollection 2020.

Abstract

AIM

To assess the non-inferiority of pitolisant, a new compound for the relief of excessive daytime sleepiness (EDS) and cataplexy in narcolepsy, compared with modafinil.

METHODS

Randomized controlled trials (RCTs) in narcolepsy were searched systematically. Network meta-analysis (NMA) compared the efficacy and safety of pitolisant and modafinil. The main endpoints are Epworth Sleepiness Scale (ESS), Maintenance of Wakefulness Test (MWT), the number of cataplexies, and overall safety.

RESULTS

Of 312 articles after removing duplicates, 10 RCTs were eligible for NMA. For ESS, a non-significant superior beneficial decrease (-0.69, [-2.18, 0.79]) showed non-inferiority of pitolisant (non-inferiority margin [NIM]=1, =0.015). An MWT beneficial increase (2.12 minutes [-0.95, 5.19]; =0.18) showed non-inferiority of pitolisant (NIM=-1). For cataplexy, the mean beneficial effect of pitolisant was significant, providing evidence of pitolisant superiority in addition to non-inferiority. The risk ratio (RR) of treatment-suspected adverse events for pitolisant/modafinil was 0.86 [0.44, 1.24] favoring pitolisant, confirming non-inferiority considering a safety margin of RR=1.25 (tolerance of 25%).

CONCLUSIONS

Pitolisant is non-inferior to modafinil in relieving EDS, but superior to modafinil in reducing cataplexy, outranking modafinil in narcolepsy type-1 patients. Despite a slight superiority of pitolisant in EDS relief, both drugs perform equally in narcolepsy type-2 patients.

摘要

目的

评估新型化合物匹莫林用于缓解发作性睡病患者日间过度嗜睡(EDS)和猝倒的效果不劣于莫达非尼。

方法

系统检索发作性睡病的随机对照试验(RCT)。网状Meta分析(NMA)比较匹莫林和莫达非尼的疗效和安全性。主要终点为埃普沃思嗜睡量表(ESS)、清醒维持试验(MWT)、猝倒发作次数和总体安全性。

结果

去除重复文献后,312篇文章中有10项RCT符合NMA纳入标准。对于ESS,匹莫林显示出非劣效性,有益下降不显著(-0.69,[-2.18, 0.79])(非劣效界值[NIM]=1,P=0.015)。MWT有益增加(2.12分钟[-0.95, 5.19];P=0.18)表明匹莫林非劣效(NIM=-1)。对于猝倒,匹莫林的平均有益效果显著,除了非劣效性外还证明了其优越性。匹莫林/莫达非尼治疗疑似不良事件的风险比(RR)为0.86 [0.44, 1.24],支持匹莫林,考虑到RR=1.25的安全边际(25%的耐受性),证实了非劣效性。

结论

匹莫林在缓解EDS方面不劣于莫达非尼,但在减少猝倒方面优于莫达非尼,在1型发作性睡病患者中优于莫达非尼。尽管匹莫林在缓解EDS方面略有优势,但两种药物在2型发作性睡病患者中的表现相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e047/7357684/7942c350ecfe/dic-2020-6-2-g001.jpg

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