Khamaysa Mohammed, Pradat Pierre-François
Laboratoire d'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, 75006 Paris, France.
Centre Référent SLA, Département de Neurologie, AP-HP, Hôpital Pitié-Salpêtrière, 75013 Paris, France.
J Pers Med. 2022 Sep 28;12(10):1601. doi: 10.3390/jpm12101601.
Amyotrophic lateral sclerosis (ALS) is an extremely heterogeneous disease of motor neurons that eventually leads to death. Despite impressive advances in understanding the genetic, molecular, and pathological mechanisms of the disease, the only drug approved to date by both the FDA and EMA is riluzole, with a modest effect on survival. In this opinion view paper, we will discuss how to address some challenges for drug development in ALS at the conceptual, technological, and methodological levels. In addition, socioeconomic and ethical issues related to the legitimate need of patients to benefit quickly from new treatments will also be addressed. In conclusion, this brief review takes a more optimistic view, given the recent approval of two new drugs in some countries and the development of targeted gene therapies.
肌萎缩侧索硬化症(ALS)是一种运动神经元的极其异质性疾病,最终会导致死亡。尽管在理解该疾病的遗传、分子和病理机制方面取得了令人瞩目的进展,但迄今为止,美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的唯一药物是利鲁唑,其对生存期的影响有限。在这篇观点论文中,我们将讨论如何在概念、技术和方法层面应对ALS药物研发中的一些挑战。此外,还将探讨与患者迫切需要从新疗法中获益相关的社会经济和伦理问题。总之,鉴于最近一些国家批准了两种新药以及靶向基因疗法的发展,这篇简短综述持更为乐观的观点。