1st Department of Neurology, School of Medicine, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
School of Medicine, University Campus, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.
Neurotherapeutics. 2022 Mar;19(2):464-475. doi: 10.1007/s13311-022-01200-3. Epub 2022 Feb 17.
Evidence for nusinersen administration in adult 5q spinal muscular atrophy (5q-SMA) patients is scarce and based on real-world observational data. The present systematic review and meta-analysis aimed to explore the efficacy and safety of nusinersen in patients older than 12 years of age with 5q-SMA. We searched MEDLINE, EMBASE, the Cochrane Library, and grey literature through April 2021. Cross-sectional studies, case reports, review articles, and studies with follow-up less than 6 months were excluded. We included 12 records (seven case-series, five cohorts) representing 11 population cohorts and enrolling 428 SMA patients. We observed statistically significant improvements on motor function Hammersmith Functional Motor Scale Expanded (HFMSE) and Revised Upper Limb Module (RULM) scores at the longest follow-up assessments [SMD = 0.17(95% CI 0.01-0.33), SMD = 0.22(95% CI 0.06-0.38), respectively]. HFMSE and RULM significant improvements were also detected at the subgroup analysis during 10 and 14 months. HFMSE and RULM amelioration occurred earlier in patients with SMA type 3 or 4 during short-term analysis (≤ 6 months). 6-min walk tests (6MWT) and pulmonary function tests did not change. Minimal clinically important differences in HFMSE and RULM were observed in 43.3% (95% CI 34.5-52.3) and 38.9% (95% CI 27.7-50.7), respectively. Severe adverse events were reported in 2% (95% CI 0-5.8). Treatment withdrawal rate was 3% (95% CI 0.5-6.6). Despite the low quality of evidence and the unmet need for randomized data to establish the safety and efficacy of nusinersen in adults, our meta-analysis confirms that nusinersen is a valuable treatment option for older patients with longer-disease duration.Trial registration: PROSPERO database CRD42020223109.
在成人 5q 型脊髓性肌萎缩症(5q-SMA)患者中使用 nusinersen 的证据很少,并且基于真实世界的观察性数据。本系统评价和荟萃分析旨在探讨 nusinersen 在 12 岁以上 5q-SMA 患者中的疗效和安全性。我们通过 2021 年 4 月在 MEDLINE、EMBASE、Cochrane 图书馆和灰色文献中进行了搜索。排除了横断面研究、病例报告、综述文章以及随访时间少于 6 个月的研究。我们纳入了 12 项记录(7 项病例系列、5 项队列),代表 11 个人群队列,共纳入 428 例 SMA 患者。我们观察到最长随访评估时运动功能的显著改善,包括 Hammersmith 功能性运动量表扩展版(HFMSE)和修订后的上肢模块(RULM)评分[SMD=0.17(95%CI 0.01-0.33),SMD=0.22(95%CI 0.06-0.38)]。在 10 个月和 14 个月的亚组分析中也检测到 HFMSE 和 RULM 的显著改善。在短期分析(≤6 个月)中,SMA 类型 3 或 4 的患者更早出现 HFMSE 和 RULM 的改善。6 分钟步行试验(6MWT)和肺功能测试没有变化。HFMSE 和 RULM 的最小临床重要差异分别为 43.3%(95%CI 34.5-52.3)和 38.9%(95%CI 27.7-50.7)。报告了 2%(95%CI 0-5.8)的严重不良事件。治疗停药率为 3%(95%CI 0.5-6.6)。尽管证据质量较低,并且需要随机数据来确定 nusinersen 在成人中的安全性和疗效,但我们的荟萃分析证实,nusinersen 是一种有价值的治疗选择,适用于疾病持续时间较长的老年患者。试验注册:PROSPERO 数据库 CRD42020223109。