University of Miami Hemophilia Treatment Center , Miami , FL , USA.
CSL Behring , King of Prussia , PA , USA.
J Med Econ. 2019 Oct;22(10):1014-1021. doi: 10.1080/13696998.2019.1620246. Epub 2019 Jun 5.
Prophylaxis with standard-acting recombinant factor IX (rFIX) in hemophilia B patients requires frequent injections. Extended half-life (EHL) products allow for prolonged dosing intervals, and so reduce this treatment burden. Three technologies are employed to extend the half-life of FIX; glycopegylation, Fc-fusion, and albumin fusion. rIX-FP is a novel albumin fusion protein, which allows for a prolonged dosing interval of up to 14 days. A systematic review and indirect statistical comparison was performed to evaluate the efficacy of both EHL and standard-acting rFIX products compared with rIX-FP in Phase III trials for prophylaxis in adult hemophilia B patients. A systematic search was conducted in both EMBASE and PubMed to identify Phase III trials of prophylactic rFIX treatment in previously treated hemophilia B patients aged ≥12 years (FIX ≤2%). Annualized bleeding rate (ABR), spontaneous ABR (AsBR), and joint ABR (AjBR) data were extracted from each study. A -test was performed using the mean of each parameter, and the mean difference in outcome between studies was calculated. Seven articles investigating six rFIX products were identified. Median ABR, AsBR, and AjBR ranged from 0-3.0, 0-1.0, and 0-1.1 (means = 0.8-4.26, 0.13-2.6, and 0.34-2.85), respectively. rIX-FP achieved the lowest median and mean values in all three parameters. -tests showed that mean ABR was significantly lower for rIX-FP 7-day prophylaxis compared with the majority of standard-acting and other EHL rFIX products. The low number of appropriate trials available for comparison limits the quantity of data available for comparison, and restricts the use of methods of adjustment for variance in study design or patient characteristics. However, these limitations are shared with similar analyses published in this field. This indirect comparison of Phase III trials indicates that rIX-FP efficacy compares favorably vs other rFIX products for prophylaxis in hemophilia B.
在乙型血友病患者中,使用标准作用的重组因子 IX(rFIX)进行预防治疗需要频繁注射。半衰期延长(EHL)产品可以延长给药间隔,从而减轻这种治疗负担。有三种技术可用于延长 FIX 的半衰期:糖基化、Fc 融合和白蛋白融合。rIX-FP 是一种新型的白蛋白融合蛋白,可将给药间隔延长至长达 14 天。进行了系统评价和间接统计比较,以评估 EHL 和标准作用的 rFIX 产品与 rIX-FP 在 III 期临床试验中预防治疗成年乙型血友病患者的疗效。在 EMBASE 和 PubMed 中进行了系统搜索,以确定之前接受过治疗的年龄≥12 岁(FIX≤2%)的乙型血友病患者中预防性 rFIX 治疗的 III 期试验。从每项研究中提取年化出血率(ABR)、自发性 ABR(AsBR)和关节 ABR(AjBR)数据。使用每个参数的平均值进行 t 检验,并计算研究之间结果的平均值差异。确定了 7 篇调查 6 种 rFIX 产品的文章。中位数 ABR、AsBR 和 AjBR 的范围为 0-3.0、0-1.0 和 0-1.1(平均值=0.8-4.26、0.13-2.6 和 0.34-2.85)。rIX-FP 在所有三个参数中均实现了最低的中位数和平均值。t 检验表明,与大多数标准作用和其他 EHL rFIX 产品相比,rIX-FP 7 天预防治疗的平均 ABR 显著降低。可用于比较的适当试验数量有限,限制了可供比较的数据量,并限制了使用调整研究设计或患者特征方差的方法。然而,这些限制与该领域发表的类似分析共享。这些 III 期试验的间接比较表明,rIX-FP 的疗效与其他 rFIX 产品相比,在乙型血友病的预防治疗方面具有优势。