Cocco Eleonora, Sardu Claudia, Spinicci Gabriella, Musu Luigina, Massa Rita, Frau Jessica, Lorefice Lorena, Fenu Giuseppe, Coghe Giancarlo, Massole Serenella, Maioli Maria Antonietta, Piras Rachele, Melis Marta, Porcu Gianluca, Mamusa Elena, Carboni Nicola, Contu Paolo, Marrosu Maria Giovanna
Multiple Sclerosis Center, ASL 8, Cagliari/ University of Cagliari, Italy.
University of Cagliari, Italy.
Mult Scler. 2015 Apr;21(4):433-41. doi: 10.1177/1352458514546788. Epub 2014 Sep 25.
A critical aspect of multiple sclerosis (MS) treatments is understanding the effect of disease-modifying drugs (DMDs) on the long-term risk of disability and whether the effect is related to disability at start of treatment.
We performed an observational study on 3060 MS patients. The effect of therapy on progression to Expanded Disability Status Scale (EDSS) 3.0 and 6.0 from onset was analysed in treated vs untreated (UTP) patients using Cox regression analysis adjusted for propensity score and immortal time bias.
Compared to UTP, the risks of EDSS 3.0 were 94% and 73% lower in immunomodulant (IMTP-) and immunosuppressant (ISTP-) treated patients, respectively, while the risk of EDSS 6.0 was 86% lower in IMTP. The risk of EDSS 6.0 was, respectively, 91% and 75% lower in 1275 IMTP before and 114 after EDSS 3.0 than in 539 UTP; the risk was higher in IMTP starting therapy after EDSS 3.0 than before (HR = 4.42).
DMDs delayed long-term disability in MS patients treated either in the early or, to a lesser extent, in the later phase of the disease. Thus, the window of therapeutic opportunity is relatively extended, assuming that early is better than late treatment, but late is better than never.
多发性硬化症(MS)治疗的一个关键方面是了解疾病修饰药物(DMDs)对长期残疾风险的影响,以及这种影响是否与治疗开始时的残疾状况相关。
我们对3060例MS患者进行了一项观察性研究。使用倾向评分和不朽时间偏倚调整后的Cox回归分析,分析了治疗组与未治疗组(UTP)患者从发病到扩展残疾状态量表(EDSS)达到3.0和6.0的进展情况。
与UTP相比,免疫调节剂(IMTP)治疗组和免疫抑制剂(ISTP)治疗组患者达到EDSS 3.0的风险分别降低了94%和73%,而IMTP治疗组达到EDSS 6.0的风险降低了86%。1275例在EDSS 3.0之前接受IMTP治疗的患者和114例在EDSS 3.0之后接受IMTP治疗的患者达到EDSS 6.0的风险分别比539例UTP患者低91%和75%;在EDSS 3.0之后开始治疗的IMTP患者的风险高于之前(风险比=4.42)。
DMDs延缓了MS患者在疾病早期或(程度较轻的)晚期接受治疗时的长期残疾。因此,假设早期治疗优于晚期治疗,但晚期治疗总比不治疗好,那么治疗机会窗口相对延长。