Ontaneda Daniel, Mowry Ellen M, Newsome Scott D, Naismith Robert T, Nicholas Jacqueline, Fisher Elizabeth, de Moor Carl, Bohn Justin, Ho Pei-Ran, Sandrock Al, Rudick Richard, Williams James R
Mellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, USA.
Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Mult Scler Relat Disord. 2022 Dec;68:104216. doi: 10.1016/j.msard.2022.104216. Epub 2022 Oct 3.
The impact of early versus later high-efficacy disease-modifying therapy (DMT) in patients with multiple sclerosis (MS) is uncertain. This study reported the association of early versus later natalizumab treatment with real-world clinical outcomes in MS patients.
The study included 661 participants diagnosed with MS in 1994 or later from 7 US centers participating in the MS Partners Advancing Technology for Health Solutions (MS PATHS) network. Time to natalizumab treatment between diagnosis and first infusion (TTNT) was determined from the Tysabri Outreach: Unified Commitment to Health (TOUCH) registry. Clinical outcomes were defined using neuroperformance tests included in the Multiple Sclerosis Performance Test. Associations were tested using TTNT as a categorical and continuous variable. Linear mixed models addressed within-subject and within-site clustering.
TTNT varied from 0.1 to 19.8 years (median [interquartile range] 4.2 [1.8, 9.0] years). A significant association between later natalizumab use and worse outcomes was demonstrated for walking speed (p < 0.001), processing speed (p < 0.001), manual dexterity (p < 0.001), brain atrophy (p = 0.001), and T2 lesion volume (p = 0.02). Covariate-adjusted modelling of a sensitivity population diagnosed with MS in 2006 or later (n = 424) demonstrated significant associations between longer TTNT and worse walking speed (p < 0.05), processing speed (p < 0.001), and manual dexterity (p < 0.001).
Later initiation of natalizumab was associated with worse clinical and radiologic imaging outcomes. Thus, high-efficacy DMT may have greater benefit when started earlier in MS patients. These results provide a rationale for randomized controlled trials to further assess the impact of early highly-effective DMT use versus later escalation of therapy.
早期与晚期高效疾病修正治疗(DMT)对多发性硬化症(MS)患者的影响尚不确定。本研究报告了早期与晚期那他珠单抗治疗与MS患者实际临床结局之间的关联。
该研究纳入了1994年或之后在美国7个参与MS伙伴推进健康解决方案技术(MS PATHS)网络的中心被诊断为MS的661名参与者。从那他珠单抗拓展计划:健康统一承诺(TOUCH)登记处确定从诊断到首次输注那他珠单抗的时间(TTNT)。临床结局使用多发性硬化症性能测试中包含的神经功能测试来定义。使用TTNT作为分类变量和连续变量来检验关联。线性混合模型处理个体内和站点内的聚类。
TTNT从0.1年至19.8年不等(中位数[四分位间距]4.2[1.8, 9.0]年)。晚期使用那他珠单抗与步行速度(p < 0.001)、处理速度(p < 0.001)、手部灵活性(p < 0.001)、脑萎缩(p = 0.001)和T2病变体积(p = 0.02)较差的结局之间存在显著关联。对2006年或之后被诊断为MS的敏感性人群(n = 424)进行协变量调整建模显示,较长的TTNT与较差的步行速度(p < 0.05)、处理速度(p < 0.001)和手部灵活性(p < 0.001)之间存在显著关联。
那他珠单抗的较晚起始与较差的临床和影像学结局相关。因此,高效DMT在MS患者中更早开始使用可能具有更大益处。这些结果为随机对照试验提供了理论依据,以进一步评估早期使用高效DMT与晚期升级治疗的影响。