Neurology, Departments of Medicine, Clinical Research, Biomedicine and Biomedical Engineering, University Hospital Basel, Basel, Switzerland.
Helsinki MS Center/The Finnish MS Society, Helsinki, Finland.
J Neurol Neurosurg Psychiatry. 2015 Nov;86(11):1202-7. doi: 10.1136/jnnp-2014-310024. Epub 2015 Sep 15.
An exploratory study of the relationship between cumulative exposure to subcutaneous (sc) interferon (IFN) β-1a treatment and other possible prognostic factors with long-term clinical outcomes in relapsing-remitting multiple sclerosis (RRMS).
Patients in the original PRISMS study were invited to a single follow-up visit 15 years after initial randomisation (PRISMS-15). Outcomes over 15 years were compared in the lowest and highest quartile of the cumulative sc IFN β-1a dose groups, and according to total time receiving sc IFN β-1a as a continuous variable per 5 years of treatment. Potential prognostic factors for outcomes were analysed.
Of 560 patients randomised in PRISMS, 291 returned for PRISMS-15 and 290 (51.8%) were analysed. Higher cumulative dose exposure and longer treatment time appeared to be associated with better outcomes on: annualised relapse rate, number of relapses, time to Expanded Disability Status Scale (EDSS) progression, change in EDSS, proportions of patients with EDSS ≥ 4 or ≥ 6, ≤ 5 relapses and EDSS <4 or <6, and time to conversion to secondary-progressive MS (SPMS). Higher dose exposure was associated with lower proportions of patients with EDSS progression and conversion to SPMS, and longer time on treatment with lower risk of first relapse. Change in EDSS from baseline to 24 months was a strong predictor of evaluated clinical outcomes over 15 years.
These findings suggest that higher cumulative exposure to sc IFN β-1a may be associated with better clinical outcomes, and early change in EDSS score may have prognostic value, over many years, in RRMS.
探索累积皮下(sc)干扰素(IFN)β-1a 治疗暴露量与其他可能的预后因素与复发性缓解型多发性硬化症(RRMS)长期临床结局之间的关系。
原 PRISMS 研究中的患者在初始随机分组后 15 年被邀请参加单次随访(PRISMS-15)。在累积 sc IFN β-1a 剂量最低和最高四分位数组中比较了 15 年内的结局,并根据每 5 年治疗时间的 sc IFN β-1a 总接受时间作为连续变量进行比较。分析了结局的潜在预后因素。
在 PRISMS 中随机分配的 560 名患者中,有 291 名患者返回参加 PRISMS-15,其中 290 名(51.8%)进行了分析。较高的累积剂量暴露和较长的治疗时间似乎与以下方面的更好结局相关:年复发率、复发次数、扩展残疾状态量表(EDSS)进展时间、EDSS 变化、EDSS≥4 或≥6的患者比例、≤5 次复发和 EDSS<4 或<6,以及向继发进展型多发性硬化症(SPMS)的转换时间。较高的剂量暴露与 EDSS 进展和向 SPMS 转化的患者比例较低,以及治疗时间较长的患者复发风险较低相关。从基线到 24 个月的 EDSS 变化是评估 RRMS 15 年内临床结局的有力预测因素。
这些发现表明,较高的累积 sc IFN β-1a 暴露量可能与更好的临床结局相关,并且 EDSS 评分的早期变化可能具有多年预后价值。