Wu Yanyu, Sun Shawn X, Fan Tao
Global Evidence & Outcomes, Data Sciences Institute, Research and Development, Takeda Development Center Americas, Inc, Cambridge, MA, USA.
US Health Economics and Outcomes Research, Takeda Pharmaceuticals USA, Inc, Lexington, MA, USA.
J Blood Med. 2022 Sep 24;13:517-524. doi: 10.2147/JBM.S359510. eCollection 2022.
US patients with hemophilia A can receive prophylaxis with extended half-life recombinant factor VIII (rFVIII) products, including efmoroctocog alfa (fragment crystallizable fusion protein) and rurioctocog alfa pegol (antihemophilic factor [recombinant], PEGylated).
To evaluate dosing patterns and weekly consumption of extended half-life rFVIII products in the United States.
We performed a retrospective analysis using the US Specialty Pharmacy Database (2015-2018). Included patients had a diagnosis of hemophilia A, ≥2 consecutive monthly claims for efmoroctocog alfa or rurioctocog alfa pegol for prophylaxis, and weight data. Outcome measures included weekly dosing frequency and dispensed weekly dose.
The analysis included 774 patients (efmoroctocog alfa, 506; rurioctocog alfa pegol, 268). Mean (SD) age was 24.2 (15.8) and 26.3 (14.9) years for patients receiving efmoroctocog alfa and rurioctocog alfa pegol, respectively; mean (SD) weight was 68.4 (36.8) and 79.8 (37.7) kg, respectively. The most frequent efmoroctocog alfa regimen was twice weekly (45.7%), followed by every 4 days (20.6%), every 3 days (9.1%), and 3 times per week (7.5%). The most frequent rurioctocog alfa pegol regimen was twice weekly (72.4%), followed by 3 times per week (8.7%), every 4 days (7.6%), and every 3 days (5.5%). The proportion of efmoroctocog alfa twice-weekly dispensing records increased from 31.5% to 50.9%, and every 4 days dispensing records decreased from 31.3% to 14.5% (2015-2018). The proportion of rurioctocog alfa pegol dispensing records remained broadly stable (2016-2018). Overall, mean (SD; median) weekly prophylactic dose was 105.4 (77.9; 92.6) IU/kg with efmoroctocog alfa, and 96.8 (41.9; 90.9) IU/kg with rurioctocog alfa pegol.
In this database study, the most frequently observed dosing frequency was twice weekly for patients receiving efmoroctocog alfa or rurioctocog alfa pegol. The observed mean weekly consumption was slightly higher, and variation was greater, in patients receiving efmoroctocog alfa versus rurioctocog alfa pegol.
美国的甲型血友病患者可接受半衰期延长的重组凝血因子VIII(rFVIII)产品进行预防治疗,包括艾美赛珠单抗(可结晶片段融合蛋白)和聚乙二醇化重组凝血因子VIII(重组抗血友病因子,聚乙二醇化)。
评估美国半衰期延长的rFVIII产品的给药模式和每周用量。
我们使用美国专科药房数据库(2015 - 2018年)进行了一项回顾性分析。纳入的患者诊断为甲型血友病,有≥2次连续每月使用艾美赛珠单抗或聚乙二醇化重组凝血因子VIII进行预防治疗的记录,以及体重数据。观察指标包括每周给药频率和每周发放剂量。
分析纳入774例患者(艾美赛珠单抗组506例,聚乙二醇化重组凝血因子VIII组268例)。接受艾美赛珠单抗和聚乙二醇化重组凝血因子VIII治疗的患者的平均(标准差)年龄分别为24.2(15.8)岁和26.3(14.9)岁;平均(标准差)体重分别为68.4(36.8)千克和79.8(37.7)千克。艾美赛珠单抗最常用的给药方案是每周两次(45.7%),其次是每4天一次(20.6%)、每3天一次(9.1%)和每周3次(7.5%)。聚乙二醇化重组凝血因子VIII最常用的给药方案是每周两次(72.4%),其次是每周3次(8.7%)、每4天一次(7.6%)和每3天一次(5.5%)。艾美赛珠单抗每周两次发放记录的比例从31.5%增至50.9%,每4天发放记录的比例从31.3%降至14.5%(2015 - 2018年)。聚乙二醇化重组凝血因子VIII发放记录的比例保持大致稳定(2016 - 2018年)。总体而言,使用艾美赛珠单抗时每周预防剂量的平均(标准差;中位数)为105.4(77.9;92.6)IU/kg,使用聚乙二醇化重组凝血因子VIII时为96.8(41.9;90.9)IU/kg。
在这项数据库研究中,接受艾美赛珠单抗或聚乙二醇化重组凝血因子VIII治疗的患者最常观察到的给药频率是每周两次。接受艾美赛珠单抗治疗的患者观察到的平均每周用量略高,且变异更大。