Department of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Ambulanzpartner Soziotechnologie APST GmbH, Berlin, Germany.
Eur J Neurol. 2021 Aug;28(8):2582-2595. doi: 10.1111/ene.14902. Epub 2021 Jun 16.
This was an investigation of treatment expectations and of the perception of therapy in adult patients with 5q-associated spinal muscular atrophy (5q-SMA) receiving nusinersen.
A prospective, non-interventional observational study of nusinersen treatment in adult 5q-SMA patients was conducted at nine SMA centers in Germany. The functional status, treatment expectations and perceived outcomes were assessed using the Amyotrophic Lateral Sclerosis Functional Rating Scale-extended (ALS-FRS-ex), the Measure Yourself Medical Outcome Profile (MYMOP2), the Treatment Satisfaction Questionnaire for Medication (TSQM-9) and the Net Promoter Score (NPS).
In all, 151 patients were included with a median age of 36 years (15-69 years). SMA type 3 (n = 90, 59.6%) prevailed, followed by type 2 (33.8%) and type 1 (6.6%). In SMA types 1-3, median ALS-FRS-ex scores were 25, 33 and 46 (of 60 scale points), respectively. MYMOP2 identified distinct treatment expectations: head verticalization (n = 13), bulbar function (n = 16), arm function (n = 65), respiration (n = 15), trunk function (n = 34), leg function (n = 76) and generalized symptoms (n = 77). Median symptom severity decreased during nusinersen treatment (median observational period 6.1 months, 0.5-16 months) from 3.7 to 3.3 MYMOP2 score points (p < 0.001). The convenience of drug administration was critical (49.7 of 100 TSQM-9 points, SD 22); however, the overall treatment satisfaction was high (74.3, SD 18) and the recommendation rating very positive (NPS +66).
Nusinersen was administered across a broad range of ages, disease durations and motor function deficits. Treatment expectations were highly differentiated and related to SMA type and functional status. Patient-reported outcomes demonstrated a positive perception of nusinersen therapy in adult patients with 5q-SMA.
本研究旨在调查接受nusinersen 治疗的 5q 相关脊髓性肌萎缩症(5q-SMA)成年患者的治疗期望和治疗感知。
在德国的 9 个 SMA 中心进行了一项前瞻性、非干预性的 nusinersen 治疗成年 5q-SMA 患者的观察性研究。使用肌萎缩侧索硬化功能评定量表扩展版(ALS-FRS-ex)、衡量自身医疗结果概况量表 2 版(MYMOP2)、药物治疗满意度问卷(TSQM-9)和净推荐值(NPS)评估患者的功能状态、治疗期望和感知结果。
共纳入 151 例患者,中位年龄 36 岁(15-69 岁)。SMA 类型 3(n=90,59.6%)最为常见,其次是类型 2(n=33,33.8%)和类型 1(n=6,6.6%)。在 SMA 类型 1-3 中,ALS-FRS-ex 评分的中位数分别为 25、33 和 46(满分 60 分)。MYMOP2 确定了不同的治疗期望:头部直立(n=13)、延髓功能(n=16)、上肢功能(n=65)、呼吸功能(n=15)、躯干功能(n=34)、下肢功能(n=76)和全身症状(n=77)。在接受 nusinersen 治疗期间(中位观察期 6.1 个月,0.5-16 个月),中位症状严重程度从 3.7 分降至 3.3 分(MYMOP2 评分,p<0.001)。药物给药的便利性至关重要(TSQM-9 得分为 49.7 分,标准差为 22);然而,总体治疗满意度较高(74.3,标准差为 18),推荐评分非常积极(NPS+66)。
nusinersen 在广泛的年龄、疾病持续时间和运动功能缺陷范围内使用。治疗期望高度分化,与 SMA 类型和功能状态相关。患者报告的结局显示,接受 nusinersen 治疗的 5q-SMA 成年患者对治疗有积极的感知。