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聚乙二醇干扰素β-1a可减少复发缓解型多发性硬化症(RRMS)患者磁共振成像(MRI)病灶演变为黑洞:来自ADVANCE研究的事后分析

Peginterferon beta-1a reduces the evolution of MRI lesions to black holes in patients with RRMS: a post hoc analysis from the ADVANCE study.

作者信息

Arnold Douglas L, You Xiaojun, Castrillo-Viguera Carmen

机构信息

Montreal Neurological Institute, McGill University, Montreal, QC, Canada.

NeuroRx Research, Montreal, QC, Canada.

出版信息

J Neurol. 2017 Aug;264(8):1728-1734. doi: 10.1007/s00415-017-8544-6. Epub 2017 Jul 7.

Abstract

The presence of chronic black holes, i.e., chronic lesions that are hypointense on T1-weighted images and are indicative of more severe tissue injury, has been increasingly utilized as a surrogate marker of therapeutic outcome in multiple sclerosis. The ADVANCE study was a 2-year, double-blind, pivotal trial evaluating the safety and efficacy of subcutaneous peginterferon beta-1a 125 mcg in 1512 patients with relapsing-remitting multiple sclerosis (RRMS). This report describes the correlation of clinical outcomes with the evolution of acute lesions into chronic black holes in ADVANCE, and the efficacy of peginterferon beta-1a in reducing this evolution. Treatment with peginterferon beta-1a significantly reduced the mean number of new/enlarging T2-weighted (NET2) lesions (0.76 vs. 1.03 from week 24, p = 0.0037; 0.44 vs. 0.99 from week 48, p < 0.0001) and new gadolinium-enhancing (Gd+) lesions (0.15 vs. 0.32 from week 24, p < 0.0001; 0.09 vs. 0.19 from week 48) that evolved into chronic black holes by 2 years. Patients with NET2 or Gd+ lesions at 24 weeks that evolved into chronic black holes showed significantly worse clinical outcomes, including a greater proportion with 12-week (14.9 vs. 8.4%; p = 0.0167) and 24-week (12.3 vs. 7.0%; p = 0.0333) confirmed disability worsening and higher mean annualized relapse rate (0.62 vs. 0.43; p = 0.0118), compared with patients with lesions that did not evolve into black holes. The correlation was independent of treatment. Reduced risk of evolution of new lesions into chronic black holes with peginterferon beta-1a treatment suggests potential to reduce long-term disability in RRMS by preventing irreversible tissue damage.

摘要

慢性黑洞的存在,即T1加权图像上呈低信号且提示更严重组织损伤的慢性病变,已越来越多地被用作多发性硬化症治疗结果的替代标志物。ADVANCE研究是一项为期2年的双盲关键试验,评估皮下注射聚乙二醇化干扰素β-1a 125 mcg对1512例复发缓解型多发性硬化症(RRMS)患者的安全性和有效性。本报告描述了ADVANCE研究中临床结果与急性病变演变为慢性黑洞的相关性,以及聚乙二醇化干扰素β-1a在减少这种演变方面的疗效。聚乙二醇化干扰素β-1a治疗显著降低了新出现/扩大的T2加权(NET2)病变的平均数量(第24周时为0.76 vs. 1.03,p = 0.0037;第48周时为0.44 vs. 0.99,p < 0.0001)以及到2年时演变为慢性黑洞的新钆增强(Gd+)病变的数量(第24周时为0.15 vs. 0.32,p < 0.0001;第48周时为0.09 vs. 0.19)。在第24周时有NET2或Gd+病变且演变为慢性黑洞的患者,其临床结果明显更差,包括12周(14.9% vs. 8.4%;p = 0.0167)和24周(12.3% vs. 7.0%;p = 0.0333)确诊残疾恶化的比例更高,以及平均年化复发率更高(0.62 vs. 0.43;p = 0.0118),与病变未演变为黑洞的患者相比。这种相关性与治疗无关。聚乙二醇化干扰素β-1a治疗降低新病变演变为慢性黑洞的风险,提示有可能通过预防不可逆组织损伤来降低RRMS患者的长期残疾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92d4/5533848/17d2903ef54b/415_2017_8544_Fig1_HTML.jpg

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