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Effects of nusinersen after one year of treatment in 123 children with SMA type 1 or 2: a French real-life observational study.123 例 SMA 1 型或 2 型患儿治疗 1 年后接受 nusinersen 的疗效:一项法国真实世界观察性研究。
Orphanet J Rare Dis. 2020 Jun 12;15(1):148. doi: 10.1186/s13023-020-01414-8.
2
Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study.Nusinersen 治疗成人 5q 型脊髓性肌萎缩症的非干预性、多中心、观察性队列研究。
Lancet Neurol. 2020 Apr;19(4):317-325. doi: 10.1016/S1474-4422(20)30037-5. Epub 2020 Mar 18.
3
244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10-12, 2019, Hoofdorp, The Netherlands.第244届ENMC国际研讨会:脊髓性肌萎缩症的新生儿筛查,2019年5月10日至12日,荷兰霍夫多普
Neuromuscul Disord. 2020 Jan;30(1):93-103. doi: 10.1016/j.nmd.2019.11.002. Epub 2019 Nov 9.
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Sitting in patients with spinal muscular atrophy type 1 treated with nusinersen.接受 nusinersen 治疗的 1 型脊髓性肌萎缩症患者。
Dev Med Child Neurol. 2020 Mar;62(3):310-314. doi: 10.1111/dmcn.14412. Epub 2019 Dec 4.
5
Nusinersen for older patients with spinal muscular atrophy: A real-world clinical setting experience.依库珠单抗治疗晚期脊髓性肌萎缩症患者的真实世界临床经验
Muscle Nerve. 2020 Feb;61(2):222-226. doi: 10.1002/mus.26769. Epub 2019 Dec 13.
6
Advances in Treatment of Spinal Muscular Atrophy - New Phenotypes, New Challenges, New Implications for Care.脊髓性肌萎缩症治疗进展——新表型、新挑战、新护理意义。
J Neuromuscul Dis. 2020;7(1):1-13. doi: 10.3233/JND-190424.
7
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study.在脊髓性肌萎缩症的前症状期对婴儿期开始用 nusinersen:2 期 NURTURE 研究的中期疗效和安全性结果。
Neuromuscul Disord. 2019 Nov;29(11):842-856. doi: 10.1016/j.nmd.2019.09.007. Epub 2019 Sep 12.
8
Evaluation of quantitative signal detection in EudraVigilance for orphan drugs: possible risk of false negatives.评估欧洲药品警戒系统(EudraVigilance)中罕见病药物的定量信号检测:假阴性的潜在风险。
Ther Adv Drug Saf. 2019 Oct 21;10:2042098619882819. doi: 10.1177/2042098619882819. eCollection 2019.
9
Clinical Evidence Supporting Early Treatment Of Patients With Spinal Muscular Atrophy: Current Perspectives.支持脊髓性肌萎缩症患者早期治疗的临床证据:当前观点
Ther Clin Risk Manag. 2019 Oct 2;15:1153-1161. doi: 10.2147/TCRM.S172291. eCollection 2019.
10
One Year of Newborn Screening for SMA - Results of a German Pilot Project.脊髓性肌萎缩症新生儿筛查的一年:德国试点项目的结果。
J Neuromuscul Dis. 2019;6(4):503-515. doi: 10.3233/JND-190428.

欧洲关于脊髓性肌萎缩症基因替代治疗的特别共识声明。

European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophy.

机构信息

Department of Neuropediatrics, University Hospital Bonn, Bonn, Germany.

Pediatric Neurology Clinic, "Prof. Dr. Al. Obregia" Hospital, Bucharest, Faculty of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.

出版信息

Eur J Paediatr Neurol. 2020 Sep;28:38-43. doi: 10.1016/j.ejpn.2020.07.001. Epub 2020 Jul 9.

DOI:10.1016/j.ejpn.2020.07.001
PMID:32763124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7347351/
Abstract

Spinal muscular atrophy (SMA) used to be one of the most common genetic causes of infant mortality. New disease modifying treatments have changed the disease trajectories and most impressive results are seen if treatment is initiated in the presymptomatic phase of the disease. Very recently, the European Medicine Agency approved Onasemnogene abeparvovec (Zolgensma®) for the treatment of patients with SMA with up to three copies of the SMN2 gene or the clinical presentation of SMA type 1. While this broad indication provides new opportunities, it also triggers discussions on the appropriate selection of patients in the context of limited available evidence. To aid the rational use of Onasemnogene abeparvovec for the treatment of SMA, a group of European neuromuscular experts presents in this paper eleven consensus statements covering qualification, patient selection, safety considerations and long-term monitoring.

摘要

脊髓性肌萎缩症(SMA)曾是导致婴儿死亡的最常见遗传病因之一。新型疾病修正治疗改变了疾病进程,如果在疾病的无症状前期启动治疗,可获得最显著的效果。最近,欧洲药品管理局批准onasemnogene abeparvovec(Zolgensma®)用于治疗携带多达三个 SMN2 基因拷贝或 SMA 类型 1 临床表现的 SMA 患者。虽然这一广泛的适应证提供了新的机会,但也引发了在有限的现有证据背景下,对患者选择的恰当性进行讨论。为了合理使用 Onasemnogene abeparvovec 治疗 SMA,一组欧洲神经肌肉专家在本文中提出了十一项共识声明,涵盖了资格、患者选择、安全性考虑因素和长期监测。