Serum neurofilament light-chain levels and long-term treatment outcomes in relapsing-remitting multiple sclerosis patients: A post hoc analysis of the randomized CombiRx trial

被引:4
作者
Cutter, Gary [1 ,2 ]
Rudick, Richard A. [3 ]
de Moor, Carl [4 ]
Singh, Carol M. [5 ]
Fisher, Elizabeth [6 ]
Koster, Thijs [7 ]
Lublin, Fred D. [8 ,9 ]
Wolinsky, Jerry S. [10 ]
McFarland, Henry [11 ]
Jacobson, Steven [12 ]
Naylor, Maria L. [7 ]
机构
[1] Univ Alabama Birmingham, Dept Biostat, 1665 Univ Blvd, Birmingham, AL 35233 USA
[2] Univ Alabama Birmingham, Sch Publ Hlth, Dept Biostat, Birmingham, AL USA
[3] Biogen Inc, Dept Neurol, Cambridge, MA USA
[4] Biogen Inc, Biostat, Cambridge, MA USA
[5] Biogen Inc, Biogen Digital Hlth, Cambridge, MA USA
[6] Biogen Inc, Value Based Med, Cambridge, MA USA
[7] Biogen Inc, Global Med, Cambridge, MA USA
[8] Corinne Goldsmith Dickinson Ctr Multiple Sclerosis, Dept Neurol, New York, NY USA
[9] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY USA
[10] Univ Texas Hlth Sci Ctr Houston UTHlth, McGovern Med Sch, Houston, TX USA
[11] Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA
[12] Natl Inst Neurol Disorders & Stroke, Viral Immunol Sect, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
Multiple sclerosis; biomarkers; treatment response; disease-modifying therapies; beta-interferon; glatiramer acetate; CEREBROSPINAL-FLUID; GLATIRAMER ACETATE; DISEASE-ACTIVITY; INTERFERON; BIOMARKERS;
D O I
10.1177/20552173231169463
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundCombiRx was a randomized, double-blind, placebo-controlled phase 3 trial in treatment-naive relapsing-remitting multiple sclerosis (RRMS) patients randomized to intramuscular interferon beta-1a (IM IFN beta-1a), glatiramer acetate (GA), or both therapies. ObjectiveThis analysis investigated changes in serum neurofilament light-chain (sNfL) levels in response to treatment and assessed baseline sNfL as a predictor of relapse. MethodsRRMS patients treated with IM IFN beta-1a 30 mu g weekly + placebo (n = 159), GA 20 mg/mL daily + placebo (n = 172), or IM IFN beta-1a + GA (n = 344) were included. A linear mixed model compared sNfL values over time. Cox regression models analyzed baseline sNfL and gadolinium-enhancing (Gd+) lesions as predictors of relapse. ResultsIn all treatment arms, the proportion of patients with sNfL >= 16 pg/mL decreased significantly from baseline to 6 months and was maintained at 36 months. A significantly higher percentage of patients with both baseline sNfL >= 16 pg/mL and >= 1 Gd+ lesion experienced relapses within 90 days compared to patients with sNfL ConclusionsNfL levels were reduced within 6 months and remained low at 36 months. Results suggest that the combination of lesion activity and sNfL was a stronger predictor of relapse than either factor alone.
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页数:9
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