Addendum to the 2023 clinical practice guidelines for amyotrophic lateral sclerosis in Japan: approval and integration of novel disease-modifying therapies.

Q4 Medicine
Clinical Neurology Pub Date : 2026-02-25 Epub Date: 2026-01-20 DOI:10.5692/clinicalneurol.cn-002198
Hitoshi Warita, Makoto Urushitani, Naoki Atsuta, Yuishin Izumi, Osamu Kano, Toshio Shimizu, Yuki Nakayama, Yugo Narita, Hiroyuki Nodera, Takuji Fujita, Koichi Mizoguchi, Mitsuya Morita, Masashi Aoki
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Abstract

Amyotrophic lateral sclerosis (ALS) is an intractable motor neuron disease characterized by progressive degeneration of motor neurons with varying degrees of frontotemporal lobe dysfunction. This English summary of the addendum to the Japanese clinical practice guidelines for ALS outlines major recent advances in pharmacological therapy in Japan. Following the development of the 2023 guidelines, three additional medications-oral edaravone, high-dose intramuscular mecobalamin, and tofersen-have been introduced. Oral edaravone, with its ease of administration, demonstrates pharmacokinetics comparable to the intravenous formulation. High-dose mecobalamin reduces functional decline when initiated early in the disease course. Tofersen, an antisense oligonucleotide, is the first gene-targeted therapy approved in Japan for patients with copper/zinc superoxide dismutase gene-related ALS, highlighting the importance of genetic testing and counseling in all ALS cases. This addendum provides updated expert consensus recommendations for the use, dosing, and monitoring of these therapies, while emphasizing the need for thorough communication about the ethical and psychological dimensions of genetic testing. It also addresses practical considerations for combination therapy, noting that up to three or four anti-ALS agents are now available in Japan. The long-term safety and efficacy of these therapies, as well as their potential synergistic or additive effects, remain to be clarified through real-world data and prospective registries. The objectives of this addendum are twofold: to present these advances and recommendations in English to foster international collaboration, and to inform the global ALS community about the latest therapeutic strategies in Japan. In addition, ongoing efforts to harmonize clinical evaluation standards and promote international clinical trials are highlighted, with the goal of improving patient outcomes and advancing ALS research worldwide.

2023年日本肌萎缩侧索硬化症临床实践指南附录:新型疾病改善疗法的批准和整合
肌萎缩性侧索硬化症(ALS)是一种顽固性运动神经元疾病,其特征是运动神经元进行性变性并伴有不同程度的额颞叶功能障碍。日本ALS临床实践指南附录的英文摘要概述了日本最近在药物治疗方面的主要进展。随着2023年指南的制定,又引入了三种额外的药物——口服依达拉奉、大剂量肌肉注射甲钴胺素和托弗森。口服依达拉奉易于给药,其药代动力学与静脉制剂相当。高剂量甲钴胺在病程早期开始治疗可减少功能衰退。Tofersen是一种反义寡核苷酸,是日本批准的首个用于铜/锌超氧化物歧化酶基因相关ALS患者的基因靶向治疗药物,突出了基因检测和咨询在所有ALS病例中的重要性。本附录就这些疗法的使用、剂量和监测提供了最新的专家共识建议,同时强调需要就基因检测的伦理和心理层面进行彻底沟通。它还解决了联合治疗的实际考虑,注意到日本目前有多达三到四种抗als药物可用。这些疗法的长期安全性和有效性,以及它们潜在的协同或附加效应,仍有待通过现实世界的数据和前瞻性注册来澄清。本增编的目的有两个:以英文介绍这些进展和建议,以促进国际合作,并向全球ALS社区通报日本最新的治疗策略。此外,还强调了协调临床评估标准和促进国际临床试验的持续努力,以改善患者预后和推进全球ALS研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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