University of California, 300 UCLA Medical Plaza B-200, Los Angeles, Los Angeles, California, USA.
PTC Therapeutics, Inc. 100 Corporate Court, South Plainfield, NJ, South Plainfield, New Jersey, USA.
Muscle Nerve. 2018 Nov;58(5):639-645. doi: 10.1002/mus.26191. Epub 2018 Sep 27.
ACT DMD was a 48-week trial of ataluren for nonsense mutation Duchenne muscular dystrophy (nmDMD). Patients received corticosteroids for ≥6 months at entry and stable regimens throughout study. This post hoc analysis compares efficacy and safety for deflazacort and prednisone/prednisolone in the placebo arm.
Patients received deflazacort (n = 53) or prednisone/prednisolone (n = 61). Endpoints included change from baseline in 6-minute walk distance (6MWD), timed function tests, estimated age at loss of ambulation (extrapolated from 6MWD).
Mean changes in 6MWD were -39.0 m (deflazacort; 95% confidence limit [CL], -68.85, -9.17) and -70.6 m (prednisone/prednisolone; 95% CL, -97.16, -44.02). Mean changes in 4-stair climb were 3.79 s (deflazacort; 95% CL, 1.54, 6.03) and 6.67 s (prednisone/prednisolone; 95% CL, 4.69, 8.64).
This analysis, limited by its post hoc nature, suggests greater preservation of 6MWD and 4-stair climb with deflazacort vs. prednisone/prednisolone. A head-to-head comparison will better define these differences. Muscle Nerve 58: 639-645, 2018.
ACT DMD 是一项为期 48 周的研究,旨在评估非义突变型杜氏肌营养不良症(nmDMD)患者中用衣拉格鲁治疗的效果。患者在入组时已接受至少 6 个月的皮质类固醇治疗,且在研究期间保持稳定的治疗方案。本事后分析比较了安慰剂组中地夫可特与泼尼松/强的松龙的疗效和安全性。
患者接受地夫可特(n=53)或泼尼松/强的松龙(n=61)治疗。主要终点包括从基线到 6 分钟步行距离(6MWD)、计时功能测试、预计丧失步行能力的年龄(从 6MWD 推断)的变化。
6MWD 的平均变化分别为-39.0m(地夫可特;95%置信区间[CL],-68.85,-9.17)和-70.6m(泼尼松/强的松龙;95% CL,-97.16,-44.02)。4 级爬梯的平均变化分别为 3.79s(地夫可特;95% CL,1.54,6.03)和 6.67s(泼尼松/强的松龙;95% CL,4.69,8.64)。
受事后分析性质的限制,本分析表明地夫可特与泼尼松/强的松龙相比,能更好地保持 6MWD 和 4 级爬梯。头对头比较将更好地定义这些差异。肌肉神经 58:639-645,2018 年。