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X-连锁肌小管肌病基因替代临床试验的起始自然史、入组研究。

INCEPTUS Natural History, Run-in Study for Gene Replacement Clinical Trial in X-Linked Myotubular Myopathy.

机构信息

Hospital for Sick Children, Toronto, Canada.

Dr. v. Haunersches Kinderspital, Klinikum der Universität München, Munich, Germany.

出版信息

J Neuromuscul Dis. 2022;9(4):503-516. doi: 10.3233/JND-210781.

DOI:10.3233/JND-210781
PMID:35694931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9398079/
Abstract

BACKGROUND

X-linked myotubular myopathy (XLMTM) is a life-threatening congenital myopathy that, in most cases, is characterized by profound muscle weakness, respiratory failure, need for mechanical ventilation and gastrostomy feeding, and early death.

OBJECTIVE

We aimed to characterize the neuromuscular, respiratory, and extramuscular burden of XLMTM in a prospective, longitudinal study.

METHODS

Thirty-four participants < 4 years old with XLMTM and receiving ventilator support enrolled in INCEPTUS, a prospective, multicenter, non-interventional study. Disease-related adverse events, respiratory and motor function, feeding, secretions, and quality of life were assessed.

RESULTS

During median (range) follow-up of 13.0 (0.5, 32.9) months, there were 3 deaths (aspiration pneumonia; cardiopulmonary failure; hepatic hemorrhage with peliosis) and 61 serious disease-related events in 20 (59%) participants, mostly respiratory (52 events, 18 participants). Most participants (80%) required permanent invasive ventilation (>16 hours/day); 20% required non-invasive support (6-16 hours/day). Median age at tracheostomy was 3.5 months (95% CI: 2.5, 9.0). Thirty-three participants (97%) required gastrostomy. Thirty-one (91%) participants had histories of hepatic disease and/or prospectively experienced related adverse events or laboratory or imaging abnormalities. CHOP INTEND scores ranged from 19-52 (mean: 35.1). Seven participants (21%) could sit unsupported for≥30 seconds (one later lost this ability); none could pull to stand or walk with or without support. These parameters remained static over time across the INCEPTUS cohort.

CONCLUSIONS

INCEPTUS confirmed high medical impact, static respiratory, motor and feeding difficulties, and early death in boys with XLMTM. Hepatobiliary disease was identified as an under-recognized comorbidity. There are currently no approved disease-modifying treatments.

摘要

背景

X 连锁肌小管肌病(XLMTM)是一种危及生命的先天性肌病,大多数情况下其特征是严重的肌肉无力、呼吸衰竭、需要机械通气和胃造口喂养,以及早期死亡。

目的

我们旨在通过前瞻性纵向研究,对 XLMTM 的神经肌肉、呼吸和肌肉外负担进行特征描述。

方法

34 名年龄<4 岁且接受呼吸机支持的 XLMTM 参与者纳入 INCEPTUS 前瞻性、多中心、非干预性研究。评估疾病相关不良事件、呼吸和运动功能、喂养、分泌物和生活质量。

结果

在中位数(范围)13.0(0.5,32.9)个月的随访期间,20 名(59%)参与者中有 3 人死亡(吸入性肺炎;心肺衰竭;肝出血伴肝血窦增生)和 61 例严重疾病相关事件,主要是呼吸系统(52 例,18 名参与者)。大多数参与者(80%)需要永久性有创通气(>16 小时/天);20%需要无创支持(6-16 小时/天)。中位数气管造口术年龄为 3.5 个月(95%CI:2.5,9.0)。33 名(97%)参与者需要胃造口。31 名(91%)参与者有肝脏疾病史和/或前瞻性地经历过相关不良事件或实验室或影像学异常。CHOP INTEND 评分为 19-52(平均:35.1)。7 名(21%)参与者可以无支撑坐 30 秒以上(其中 1 名后来失去了这种能力);无人可以独立站立或行走。这些参数在 INCEPTUS 队列中随时间保持静态。

结论

INCEPTUS 证实了 XLMTM 男孩的高医疗影响、静态呼吸、运动和喂养困难以及早期死亡。肝胆疾病被确定为一种未被充分认识的合并症。目前尚无批准的疾病修饰治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/9398079/609911aacb18/jnd-9-jnd210781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/9398079/a82ebc4ae438/jnd-9-jnd210781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/9398079/609911aacb18/jnd-9-jnd210781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/9398079/a82ebc4ae438/jnd-9-jnd210781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1d/9398079/609911aacb18/jnd-9-jnd210781-g002.jpg

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本文引用的文献

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Hepatobiliary disease in XLMTM: a common comorbidity with potential impact on treatment strategies.XLMTM 相关肝胆疾病:一种常见的合并症,可能对治疗策略产生影响。
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High-throughput transcriptome analyses from ASPIRO, a phase 1/2/3 study of gene replacement therapy for X-linked myotubular myopathy.ASPIRO 研究的高通量转录组分析,这是一项针对 X 连锁肌小管肌病基因替代治疗的 1/2/3 期研究。
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