Center for Experimental Neurotherapeutics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Division of Neurology, Nemours Children's Hospital, Orlando, FL, USA.
J Neuromuscul Dis. 2023;10(3):389-404. doi: 10.3233/JND-221560.
Spinal muscular atrophy (SMA) is a neuromuscular disorder arising from biallelic non-functional survival motor neuron 1 (SMN1) genes with variable copies of partially functional SMN2 gene. Intrathecal onasemnogene abeparvovec administration, at fixed, low doses, may enable treatment of heavier patients ineligible for weight-based intravenous dosing.
STRONG (NCT03381729) assessed the safety/tolerability and efficacy of intrathecal onasemnogene abeparvovec for sitting, nonambulatory SMA patients.
Sitting, nonambulatory SMA patients (biallelic SMN1 loss, three SMN2 copies, aged 6-<60 months) received a single dose of intrathecal onasemnogene abeparvovec. Patients were enrolled sequentially into one of three (low, medium, and high) dose cohorts and stratified into two groups by age at dosing: younger (6-<24 months) and older (24-<60 months). Primary endpoints included safety/tolerability, independent standing ≥3 seconds (younger group), and change in Hammersmith Functional Motor Scale Expanded (HFMSE) from baseline (older group) compared with historic controls.
Thirty-two patients were enrolled and completed the study (medium dose, n = 25). All patients had one or more treatment-emergent adverse events, with one serious and related to treatment (transaminase elevations). No deaths were reported. One of 13 patients (7.7%) in the younger group treated with the medium dose achieved independent standing. At Month 12 for the older group receiving the medium dose, change from baseline in HFMSE was significantly improved compared with the SMA historic control population (P < 0.01).
Intrathecal onasemnogene abeparvovec was safe and well-tolerated. Older patients treated with the medium dose demonstrated increases in HFMSE score greater than commonly observed in natural history.
脊髓性肌萎缩症(SMA)是一种由双等位基因无功能存活运动神经元 1(SMN1)基因引起的神经肌肉疾病,其具有部分功能的 SMN2 基因的可变拷贝数。鞘内注射onasemnogene abeparvovec 以固定的低剂量给药,可能使不符合基于体重静脉给药条件的更重患者得到治疗。
STRONG(NCT03381729)评估了鞘内注射onasemnogene abeparvovec 治疗不能坐立、不能行走的 SMA 患者的安全性/耐受性和疗效。
不能坐立、不能行走的 SMA 患者(双等位基因 SMN1 缺失,SMN2 基因有三个拷贝,年龄为 6-<60 个月)接受了一次鞘内注射 onasemnogene abeparvovec。患者按顺序被纳入三个剂量队列之一(低、中、高),并按给药时的年龄分为两组:年龄较小(6-<24 个月)和年龄较大(24-<60 个月)。主要终点包括安全性/耐受性、年轻组独立站立≥3 秒,以及年长组基线至治疗后 12 个月时的改良 Hammersmith 功能运动量表(HFMSE)评分变化,与历史对照相比。
共 32 例患者入组并完成了研究(中剂量组,n = 25)。所有患者均出现 1 次或多次治疗相关不良事件,1 例严重且与治疗相关(转氨酶升高)。无死亡报告。中剂量组中 13 例患者中有 1 例(7.7%)达到了独立站立。中剂量组年长组在治疗后 12 个月时,与 SMA 历史对照组相比,HFMSE 评分的基线变化显著改善(P < 0.01)。
鞘内注射 onasemnogene abeparvovec 安全且耐受良好。接受中剂量治疗的年长患者 HFMSE 评分的增加大于自然史中通常观察到的水平。