a Parexel International (Heron commercialization) , Chandigarh , UT , India.
b Parexel International , London , UK.
Curr Med Res Opin. 2018 Aug;34(8):1361-1371. doi: 10.1080/03007995.2017.1407303. Epub 2017 Nov 28.
To assess the comparative efficacy and safety of cladribine tablets versus alternative disease modifying treatments (DMTs) in patients with active relapsing-remitting multiple sclerosis (RRMS), and in a subgroup with high disease activity (HRA + DAT), using systematic literature review (SLR) and network meta-analysis (NMA).
MEDLINE, Embase, MEDLINE In-Process and CENTRAL databases were systematically searched to identify English-language publications of relevant studies of approved DMTs for RRMS. Searches were conducted from database inception to January 2017. Conference websites and trial registries were also searched. NMA considered the effects of DMTs on annualized relapse rate (ARR), confirmed disease progression (CDP), no evidence of disease activity (NEDA) and safety.
Of 10,825 articles retrieved and screened, 44 studies assessing 12 DMTs contributed to the NMA. In patients with active RRMS, cladribine tablets were associated with a significant 58% reduction in ARR versus placebo (p < .05); cladribine tablets were similar or significantly better than other DMT regimens and ranked fourth among DMTs, behind alemtuzumab, natalizumab and ocrelizumab. For CDP for 6 months and NEDA, improvements with cladribine tablets were significantly greater than those of placebo (p < .05), with no comparator DMT demonstrating significantly better results. Similar findings were reported in the HRA + DAT population. Overall adverse event risk for cladribine tablets did not differ significantly from that of placebo and most alternative DMTs.
In this first NMA to consider cladribine tablets, ocrelizumab and daclizumab for treatment of RRMS, cladribine tablets are a comparatively effective and safe alternative to other DMTs in both active RRMS and HRA + DAT populations.
通过系统文献回顾(SLR)和网络荟萃分析(NMA)评估克拉屈滨片与其他疾病修正治疗(DMT)在活动性复发缓解型多发性硬化症(RRMS)患者中的疗效和安全性差异,并在高疾病活动度(HRA+DAT)亚组中进行评估。
系统检索 MEDLINE、Embase、MEDLINE In-Process 和 CENTRAL 数据库,以识别 RRMS 已批准 DMT 的相关研究的英文文献。检索从数据库建立到 2017 年 1 月。还检索了会议网站和试验注册处。NMA 考虑了 DMT 对年化复发率(ARR)、确诊疾病进展(CDP)、无疾病活动证据(NEDA)和安全性的影响。
从检索和筛选的 10825 篇文章中,44 项评估 12 种 DMT 的研究纳入 NMA。在活动性 RRMS 患者中,与安慰剂相比,克拉屈滨片可显著降低 58%的 ARR(p<0.05);与其他 DMT 方案相比,克拉屈滨片相似或明显更好,在 DMT 中排名第四,仅次于阿仑单抗、那他珠单抗和奥瑞珠单抗。在 6 个月时 CDP 和 NEDA,克拉屈滨片的改善明显优于安慰剂(p<0.05),且没有一种比较的 DMT 显示出明显更好的结果。在 HRA+DAT 人群中也报告了类似的发现。克拉屈滨片的总体不良事件风险与安慰剂和大多数其他 DMT 无显著差异。
在首次考虑克拉屈滨片、奥瑞珠单抗和达利珠单抗治疗 RRMS 的 NMA 中,与其他 DMT 相比,克拉屈滨片在活动性 RRMS 和 HRA+DAT 人群中是一种相对有效的替代治疗方法。