CHU of Caen, Avenue de la Côte de Nacre, Caen 14033, France.
Strasbourg University, 4 Rue Kirschleger, Strasbourg 67000, France.
Mult Scler Relat Disord. 2018 Oct;25:276-281. doi: 10.1016/j.msard.2018.08.004. Epub 2018 Aug 6.
Despite a recent interest in Real World Data, such studies are scarce in multiple sclerosis (MS) disease. The objective was to describe the patients, disease progression and use of DMDs in France and compare clinical effectiveness of first-line injectable DMDs.
We conducted a retrospective multicenter study in France, using data collected by 11 expert centers with the EDMUS software.
Overall, 15,039 French MS patients were followed for a mean of 11.5 years. Mean age at start of disease was 32 years and 74% were women. After the disease onset, median time to reach EDSS 3 was 11 years and 51.8% of patients were relapse-free 2 years after the disease's onset. The mean delay between onset of disease and initiation of treatment was 5.7 ± 6.9 years. Over time, it decreased from 8.8 ± 7.8 to 0.7 ± 0.7 years for initiation of treatment before 2000 vs. after 2010, respectively. Two years after the initiation of treatment, the persistence rate of injectable disease modifying drugs (DMDs) was 60.7%. The effectiveness of these drugs were quite similar.
This study brings new insight on the natural history of MS and the use and effectiveness of injectable DMDs in this condition.
尽管最近对真实世界数据(Real World Data)产生了兴趣,但在多发性硬化症(MS)领域,此类研究仍然很少。本研究旨在描述法国患者的特征、疾病进展情况和 DMD 的使用情况,并比较一线注射用 DMD 的临床疗效。
我们在法国开展了一项回顾性多中心研究,使用由 11 个专家中心使用 EDMUS 软件收集的数据。
总体而言,15039 名法国 MS 患者的平均随访时间为 11.5 年。发病时的平均年龄为 32 岁,74%为女性。发病后,中位时间达到 EDSS3 为 11 年,51.8%的患者在发病后 2 年内无复发。疾病开始到开始治疗的平均延迟为 5.7±6.9 年。随着时间的推移,从 2000 年之前的 8.8±7.8 年降至 2010 年后的 0.7±0.7 年。治疗开始后 2 年内,注射用疾病修饰药物(DMD)的持续使用率为 60.7%。这些药物的疗效相当相似。
本研究为 MS 的自然病史以及在这种情况下使用和有效性提供了新的见解。