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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.

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。

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