Butler Oisín, Heeg Simone, Holl Katsiaryna, Frenz Ann-Kathrin, Wicklein Eva-Maria, Rametta Mark, Yeo Sandy
Medical Affairs and Pharmacovigilance, Pharmaceuticals, RWE Strategy & Outcomes Data Generation, Bayer AG, Building P300, 13342, Berlin, Germany.
Research and Development, Bayer AG, Berlin, Germany.
Drugs Real World Outcomes. 2021 Sep;8(3):359-367. doi: 10.1007/s40801-021-00248-5. Epub 2021 Apr 29.
Both interferon beta-1b (IFN-β-1b) and interferon beta-1a (IFN-β-1a) are immunomodulators that require regular subcutaneous self-administration by patients with multiple sclerosis (MS). However, no electronic autoinjector is available for IFN-β-1a in the US.
This retrospective cohort study investigated adherence to two subcutaneous disease-modifying therapies, IFN-β-1b and IFN-β-1a, during two periods (before and after the introduction of the BETACONNECT autoinjector for IFN-β-1b).
Data were evaluated from the MarketScan database for adults in the US with an MS diagnosis and a medical claim for subcutaneous IFN-β-1b or IFN-β-1a, either before (October 2013-September 2015) or after the introduction of BETACONNECT (October 2016-September 2018). Patient populations were propensity-score matched by demographic and clinical characteristics. Persistence was recorded, and adherence was evaluated by medication possession ratio (MPR).
The study included 196 IFN-β-1b and 365 IFN-β-1a people with MS (PwMS) (pre-BETACONNECT period), and 126 IFN-β-1b and 223 IFN-β-1a PwMS (post-BETACONNECT period). In the pre-BETACONNECT period, the proportion with at least 80% MPR was higher for IFN-β-1a (90%) than for IFN-β-1b (83%), but in the post-BETACONNECT period the proportion with ≥ 80% MPR was higher for IFN-β-1b (92%) than for IFN-β-1a (86%). In the pre-BETACONNECT period, median persistence (in days) was higher for IFN-β-1a (199) than for IFN-β-1b (152), while in post-BETACONNECT period persistence was higher for IFN-β-1b (327) than for IFN-β-1a (229).
Following the introduction of BETACONNECT, this exploratory study suggested that PwMS taking IFN-β-1b were more adherent compared with those taking IFN-β-1a, with higher persistence, and more than 90% reached 80% MPR, a threshold commonly used to define good adherence.
干扰素β-1b(IFN-β-1b)和干扰素β-1a(IFN-β-1a)均为免疫调节剂,多发性硬化症(MS)患者需要定期自行皮下注射。然而,在美国,尚无用于IFN-β-1a的电子自动注射器。
这项回顾性队列研究调查了在两个时期(IFN-β-1b的BETACONNECT自动注射器推出之前和之后)两种皮下疾病改善疗法IFN-β-1b和IFN-β-1a的依从性。
数据来自美国MarketScan数据库中诊断为MS且有皮下注射IFN-β-1b或IFN-β-1a医疗索赔的成年人,数据收集时间为BETACONNECT推出之前(2013年10月至2015年9月)或之后(2016年10月至2018年9月)。根据人口统计学和临床特征对患者群体进行倾向评分匹配。记录持续用药情况,并通过药物持有率(MPR)评估依从性。
该研究纳入了196例使用IFN-β-1b的MS患者(PwMS)和365例使用IFN-β-1a的PwMS(BETACONNECT推出前时期),以及126例使用IFN-β-1b的PwMS和223例使用IFN-β-1a的PwMS(BETACONNECT推出后时期)。在BETACONNECT推出前时期,MPR至少为80%的IFN-β-1a使用者比例(90%)高于IFN-β-1b使用者(83%),但在BETACONNECT推出后时期,MPR≥80%的IFN-β-1b使用者比例(92%)高于IFN-β-1a使用者(86%)。在BETACONNECT推出前时期,IFN-β-1a的中位持续用药天数(199天)高于IFN-β-1b(152天),而在BETACONNECT推出后时期,IFN-β-1b的持续用药天数(327天)高于IFN-β-1a(229天)。
在引入BETACONNECT之后,这项探索性研究表明,与使用IFN-β-1a的PwMS相比,使用IFN-β-1b的PwMS依从性更高,持续用药时间更长,超过90%的人达到了80%的MPR,这是常用于定义良好依从性的阈值。