Hupperts Raymond, Ghazi-Visser Lizette, Martins Silva Ana, Arvanitis Michalis, Kuusisto Hanna, Marhardt Kurt, Vlaikidis Nikolaos
Orbis Medical Centre, Sittard-Geleen, Maastricht University Medical Centre, the Netherlands.
Merck BV Schiphol-Rijk, the Netherlands.
Clin Ther. 2014 Dec 1;36(12):1946-1957. doi: 10.1016/j.clinthera.2014.04.002. Epub 2014 May 5.
Adverse reactions, particularly injection site reactions (ISRs), are common reasons for nonadherence to injectable multiple sclerosis (MS) treatments. Adherence to MS treatment is important to ensure good treatment outcomes.
The aim of this study was to assess the local tolerability of subcutaneous (SC) serum-free interferon (IFN) β-1a in patients with relapsing MS over 1 year in a real-life, international setting. The study also assessed safety, disease activity, and adherence.
This was a prospective, international, multicenter, observational study of 251 patients with relapsing-remitting MS treated with SC serum-free IFN β-1a 44 μg or 22 μg 3 times weekly for 12 months or until early discontinuation. The primary end point was the proportion of patients with ISRs. Secondary end points included proportion of patients with adverse events (AEs); annualized relapse rate (ARR); proportion of patients remaining relapse-free; and adherence to treatment.
During the observation period, 27.5% (69 of 251) of patients experienced nonserious ISRs, which was consistent with the incidence reported in clinical studies. Five patients discontinued treatment and 2 patients suspended treatment because of ISRs. Mean age was 35.8 years; patients were predominantly white (94.8%), and two thirds (66.1%) were female. The overall incidence of AEs was 63.7% (160 of 251), and overall safety and tolerability were assessed as excellent, very good, or good in >85% of patients. More than 70% of patients remained relapse-free, and the mean ARR was 0.4. More than 90% of patients had very good or good adherence to treatment; a significantly greater proportion of these were relapse-free at 12 months compared with those with fair or poor adherence (77.6% vs 50.0%; P = 0.0107), and their ARR was significantly lower (0.3 vs 0.9; P = 0.0055). Patients with fair or poor adherence had 4.6 times higher odds of experiencing a relapse than those with very good or good adherence.
The incidence of ISRs and the overall safety profile in this observational study, in an international population in a real-life setting, confirm the good local tolerability of SC serum-free IFN β-1a reported in clinical studies. The association between good adherence and a lower ARR underlines the importance of good adherence. The good local and general tolerability of SC IFN β-1a may help ensure a high level of adherence, which is associated with better clinical outcomes. ClinicalTrials.gov identifier: NCT01080027.
不良反应,尤其是注射部位反应(ISR),是导致不坚持注射用多发性硬化症(MS)治疗的常见原因。坚持MS治疗对于确保良好的治疗效果很重要。
本研究的目的是在现实生活中的国际环境下,评估皮下注射(SC)无血清干扰素(IFN)β-1a在复发型MS患者中1年的局部耐受性。该研究还评估了安全性、疾病活动度和依从性。
这是一项前瞻性、国际性、多中心的观察性研究,对251例复发缓解型MS患者进行治疗,患者接受每周3次皮下注射44μg或22μg无血清IFNβ-1a,持续12个月或直至提前停药。主要终点是发生ISR的患者比例。次要终点包括发生不良事件(AE)的患者比例、年化复发率(ARR)、无复发患者比例以及治疗依从性。
在观察期内,27.5%(251例中的69例)的患者出现非严重ISR,这与临床研究报告的发生率一致。5例患者因ISR停药,2例患者因ISR暂停治疗。平均年龄为35.8岁;患者主要为白人(94.8%),三分之二(66.1%)为女性。AE的总体发生率为63.7%(251例中的160例),超过85%的患者总体安全性和耐受性被评估为优秀、非常好或良好。超过70%的患者无复发,平均ARR为0.4。超过90%的患者对治疗的依从性非常好或良好;与依从性一般或较差的患者相比,这些患者在12个月时无复发的比例显著更高(77.6%对50.0%;P = 0.0107),且他们的ARR显著更低(0.3对0.9;P = 0.0055)。依从性一般或较差的患者复发的几率是依从性非常好或良好患者的4.6倍。
在现实生活环境中的国际人群中进行的这项观察性研究中,ISR的发生率和总体安全性概况证实了临床研究中报告的SC无血清IFNβ-1a良好的局部耐受性。良好的依从性与较低的ARR之间的关联强调了良好依从性的重要性。SC IFNβ-1a良好的局部和总体耐受性可能有助于确保高水平的依从性,这与更好的临床结果相关。ClinicalTrials.gov标识符:NCT01080027。