Department of Neurology, Danish Multiple Sclerosis Center, Rigshospitalet, University of Copenhagen, Copenhagen.
Department of Neurology, The Danish Multiple Sclerosis Registry, Rigshospitalet, University of Copenhagen, Copenhagen.
Eur J Neurol. 2018 Oct;25(10):1262-e110. doi: 10.1111/ene.13692. Epub 2018 Jul 9.
To assess long-term treatment effectiveness of disease-modifying therapy (DMT) initiated early in disease course versus later treatment start.
We included all Danish patients with multiple sclerosis (MS) treated with DMT through two nationwide population-based MS registries. Patients were categorized as early treated if treatment started within 2 years after the first MS symptom (n = 2316) and later treated if treatment started between 2 and 8 years after clinical onset (n = 1479). We compared time from treatment start to progression to an Expanded Disability Status Scale (EDSS) score of 6 and mortality between cohorts as hazard ratio (HR) using a Cox proportional hazards model with adjustment for stabilized inverse probability of treatment weights. Several sensitivity analyses were conducted.
The median follow-up time of 3795 patients was 7.0 (range 0.6-19.5) years for the EDSS score of 6 outcome and 10.4 (range 1.2-20.1) years for the mortality outcome. Patients with later treatment start showed a 42% increased hazard rate of reaching an EDSS score of 6 compared with the early-treated patients [HR, 1.42; 95% confidence interval (CI), 1.18-1.70; P < 0.001]. When stratified by sex, the increased hazard among later-treated women persisted (HR, 1.53; 95% CI, 1.22-1.93; P < 0.001), whereas the HR was lower in men (1.25; 95% CI, 0.93-1.69; P = 0.15). Mortality was increased by 38% in later starters (HR, 1.38; 95% CI, 0.96-1.99; P = 0.08).
Patients who started treatment with DMT later reached an EDSS score of 6 more quickly compared with patients who started early and the delay showed a tendency to shorten time to death. Our results support the use of early treatment.
评估疾病修饰疗法(DMT)在疾病早期开始与晚期开始的长期治疗效果。
我们纳入了通过两个全国性多发性硬化症(MS)注册中心接受 DMT 治疗的所有丹麦 MS 患者。如果治疗开始于首次 MS 症状后 2 年内(n = 2316),则将患者归类为早期治疗;如果治疗开始于临床发病后 2 至 8 年内(n = 1479),则归类为晚期治疗。我们使用 Cox 比例风险模型比较了两个队列之间从治疗开始到扩展残疾状况量表(EDSS)评分达到 6 分的时间和死亡率,并使用稳定的逆概率治疗权重调整了风险比(HR)。进行了几项敏感性分析。
3795 名患者的中位随访时间为 EDSS 评分 6 分的结局为 7.0 年(范围 0.6-19.5),死亡率的结局为 10.4 年(范围 1.2-20.1)。与早期治疗患者相比,晚期治疗患者达到 EDSS 评分 6 分的风险率增加了 42%[HR,1.42;95%置信区间(CI),1.18-1.70;P < 0.001]。按性别分层时,晚期治疗女性的风险增加仍然持续(HR,1.53;95% CI,1.22-1.93;P < 0.001),而男性的 HR 较低(1.25;95% CI,0.93-1.69;P = 0.15)。晚期治疗患者的死亡率增加了 38%(HR,1.38;95% CI,0.96-1.99;P = 0.08)。
与早期开始治疗的患者相比,晚期开始 DMT 治疗的患者更快地达到 EDSS 评分 6 分,且这种延迟显示出缩短死亡时间的趋势。我们的结果支持早期治疗。