UCB Pharma, Brussels, Belgium.
Mid-Atlantic Epilepsy and Sleep Center, Bethesda, Maryland.
Epilepsia. 2020 Apr;61(4):595-609. doi: 10.1111/epi.16476. Epub 2020 Mar 22.
Head-to-head randomized controlled trials (RCTs) are the gold standard for assessing comparative treatment effects. In the absence of direct comparisons between all possible antiepileptic drugs (AEDs), however, clinical decision-making in focal (partial onset) epilepsy relies on alternative evidence borne from indirect comparisons including network meta-analyses (NMAs) and from real-world evidence (RWE) studies. We review NMAs and observational RWE studies comparing AEDs in the adjunctive setting to compare the robustness of these methods and to formulate recommendations for future evidence development.
A literature review identified NMAs and RWE studies comparing AEDs for the adjunctive treatment of focal seizures published between January 2008 and October 2018. NMAs were evaluated for robustness using a framework based on guidelines from the National Institute for Health and Care Excellence Decision Support Unit and the International Society for Pharmacoeconomics and Outcomes Research. RWE studies were evaluated using the GRACE checklist.
From a total of 1993 records, 11 NMAs and six RWE studies were eligible. Key limitations identified in the NMAs include nonsystematic selection of RCTs, unexplored heterogeneity between included RCTs in terms of study and patient characteristics, and selection of AEDs and AED doses or dosing strategies that are not reflective of clinical practice. The main limitations of RWE studies concern sample size, design, and analysis methods. Approximately 90% of comparisons between individual AEDs were nonsignificant in the NMAs. None of the RWE studies adjusted for baseline differences between comparator groups; therefore, they lack the validity to make comparative conclusions.
Current NMAs and RWE studies provide only nominal comparative evidence for AED treatments in focal epilepsy, and should be used with caution for decision-making due to their methodological limitations. To overcome these hurdles, adherence to methodological guidelines and concerted efforts to collect relevant outcome data in the real world are needed.
头对头随机对照试验(RCT)是评估比较治疗效果的金标准。然而,由于无法对所有可能的抗癫痫药物(AED)进行直接比较,因此在局灶性(部分发作)癫痫的临床决策中,依赖于间接比较的替代证据,包括网络荟萃分析(NMA)和真实世界证据(RWE)研究。我们回顾了比较辅助治疗局灶性发作时 AED 的 NMA 和观察性 RWE 研究,以比较这些方法的稳健性,并为未来的证据制定建议。
文献检索确定了 2008 年 1 月至 2018 年 10 月期间发表的比较辅助治疗局灶性癫痫时 AED 的 NMA 和 RWE 研究。使用基于英国国家卫生与保健优化研究所决策支持单位和国际药物经济学和结果研究学会指南的框架评估 NMA 的稳健性。使用 GRACE 清单评估 RWE 研究。
从总共 1993 条记录中,有 11 项 NMA 和 6 项 RWE 研究符合条件。在 NMA 中发现的关键局限性包括 RCT 的非系统性选择、纳入 RCT 在研究和患者特征方面未探索的异质性,以及选择的 AED 及其剂量或给药方案与临床实践不符。RWE 研究的主要局限性涉及样本量、设计和分析方法。在 NMA 中,大约 90%的个别 AED 比较无显著性差异。没有一项 RWE 研究调整了比较组之间的基线差异;因此,它们缺乏进行比较结论的有效性。
目前的 NMA 和 RWE 研究仅为局灶性癫痫的 AED 治疗提供了名义上的比较证据,由于其方法学局限性,在决策时应谨慎使用。为了克服这些障碍,需要遵守方法学指南并共同努力在现实世界中收集相关的结局数据。