Switching therapies: safety profile of Onasemnogene abeparvovec-xioi in a SMA1 patient previously treated with Risdiplam.

Q3 Medicine
Acta Myologica Pub Date : 2022-09-30 eCollection Date: 2022-01-01 DOI:10.36185/2532-1900-077
Michele Tosi, Michela Catteruccia, Claudio Cherchi, Irene Mizzoni, Adele D'Amico
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引用次数: 5

Abstract

Three disease-modifying drugs (Nusinersen, Risdiplam and Onasemnogene abeparvovec) have been approved for SMA type I. Onasemnogene abeparvovec (GRT) can be administered in naïve patients or patients who are already being treated with Nusinersen or Risdiplam. Safety data on GRT in naïve patients or previously treated Nusinersen have been extensively described whereas any case of switch therapy from Risdiplam to GRT has been reported yet. We report on a SMA type I patient treated with Risdiplam by 2 months and switched to GRT at 5 months. She manifested the more common and awaited side effects that resolved in 3 months. The follow-up after 9 months from GRT infusion showed normal blood count, renal and cardiac function. She had great improvement in motor outcome, and no respiratory and bulbar problems as well as normal neurocognitive profile. This case suggests that the GRT may be safe also in patients previously treated with Risdiplam.

转换疗法:Onasemnogene abparvovec -xioi在先前接受Risdiplam治疗的SMA1患者中的安全性
三种疾病改善药物(Nusinersen, Risdiplam和Onasemnogene abparvovec)已被批准用于i型SMA。Onasemnogene abparvovec (GRT)可用于naïve患者或已经接受Nusinersen或Risdiplam治疗的患者。naïve患者或先前接受过Nusinersen治疗的GRT的安全性数据已被广泛描述,而从Risdiplam转换治疗到GRT的任何病例尚未报道。我们报告了一名1型SMA患者,在接受Risdiplam治疗2个月后,在5个月时改用GRT。她表现出更常见和等待的副作用,并在3个月后消退。GRT输注9个月后随访,血球计数、肾功能、心功能正常。她的运动预后有很大改善,没有呼吸和球的问题以及正常的神经认知特征。该病例提示,GRT对于先前接受过利斯地普兰治疗的患者可能也是安全的。
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
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
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