Department of Neurology, Strasbourg University Hospitals, 1 avenue Molière, Strasbourg 67200, France.
Department of Neurology, Strasbourg University Hospitals, 1 avenue Molière, Strasbourg 67200, France.
Mult Scler Relat Disord. 2023 Nov;79:104942. doi: 10.1016/j.msard.2023.104942. Epub 2023 Aug 13.
Pediatric forms of multiple sclerosis are more active than those in adults. Yet, the effectiveness of different therapeutic approaches is not well studied in this population. Our objective was to compare the effectiveness of the early use of high efficacy therapies (HETs) with the effectiveness of moderate efficacy therapies (METs) in children with MS.
This observational study included patients diagnosed with pediatric MS, at 4 hospital centers in France, during a 10-year period. METs included: interferon β-1a, glatiramer acetate, dimethyl fumarate, teriflunomide; HETs included: fingolimod, natalizumab, ocrelizumab, alemtuzumab. The primary endpoint was the occurrence of a new relapse, the secondary endpoint was EDSS worsening.
Sixty-four patients were included in the analysis (80% women; mean age 15.5 years, 81% treated with MET) with a median follow-up of 22.5 months. At baseline, 52 patients were on MET (interferon β-1a, glatiramer acetate, dimethyl fumarate, teriflunomide) and 12 patients were on HET (natalizumab, ocrelizumab). The cumulative probability of being relapse-free at 6.5 years was 23.3% on MET, vs 90.9% on HET (p = 0.013). The cumulative probability of no EDSS worsening did not differ between the 2 groups.
Patients starting with METs had much higher clinical disease activity than those starting early with HETs. Rapid initiation of more aggressive treatment may allow better disease control; however, the data on EDSS worsening are not conclusive.
儿科多发性硬化症比成人多发性硬化症更活跃。然而,在这一人群中,不同治疗方法的效果尚未得到很好的研究。我们的目的是比较早期使用高效治疗药物(HET)与中度疗效治疗药物(MET)在儿童多发性硬化症中的疗效。
本观察性研究纳入了在法国 4 家医院中心诊断为儿科多发性硬化症的患者,研究时间为 10 年。MET 包括:干扰素β-1a、那他珠单抗、醋酸格拉替雷、富马酸二甲酯、特立氟胺;HET 包括:芬戈莫德、那他珠单抗、奥瑞珠单抗、阿仑单抗。主要终点是新的复发,次要终点是 EDSS 恶化。
共纳入 64 例患者进行分析(80%为女性;平均年龄 15.5 岁,81%接受 MET 治疗),中位随访时间为 22.5 个月。基线时,52 例患者接受 MET(干扰素β-1a、醋酸格拉替雷、富马酸二甲酯、特立氟胺),12 例患者接受 HET(那他珠单抗、奥瑞珠单抗)。MET 组 6.5 年无复发的累积概率为 23.3%,HET 组为 90.9%(p=0.013)。两组间 EDSS 无恶化的累积概率无差异。
起始使用 MET 的患者临床疾病活动度明显高于起始使用 HET 的患者。早期使用更积极的治疗方法可能会更好地控制疾病;然而,EDSS 恶化的数据尚无定论。