Kishnani Priya S, Corzo Deya, Leslie Nancy D, Gruskin Daniel, Van der Ploeg Ans, Clancy John P, Parini Rosella, Morin Gilles, Beck Michael, Bauer Mislen S, Jokic Mikael, Tsai Chen-En, Tsai Brian W H, Morgan Claire, O'Meara Tara, Richards Susan, Tsao Elisa C, Mandel Hanna
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710, USA.
Pediatr Res. 2009 Sep;66(3):329-35. doi: 10.1203/PDR.0b013e3181b24e94.
In a previous 52-wk trial, treatment with alglucosidase alpha markedly improved cardiomyopathy, ventilatory function, and overall survival among 18 children <7 mo old with infantile-onset Pompe disease. Sixteen of the 18 patients enrolled in an extension study, where they continued to receive alglucosidase alpha at either 20 mg/kg biweekly (n = 8) or 40 mg/kg biweekly (n = 8), for up to a total of 3 y. These children continued to exhibit the benefits of alglucosidase alpha at the age of 36 mo. Cox regression analyses showed that over the entire study period, alglucosidase alpha treatment reduced the risk of death by 95%, reduced the risk of invasive ventilation or death by 91%, and reduced the risk of any type of ventilation or death by 87%, compared with an untreated historical control group. Cardiomyopathy continued to improve and 11 patients learned and sustained substantial motor skills. No significant differences in either safety or efficacy parameters were observed between the 20 and 40 mg/kg biweekly doses. Overall, long-term alglucosidase alpha treatment markedly extended survival as well as ventilation-free survival and improved cardiomyopathy.
在之前一项为期52周的试验中,用阿糖苷酶α进行治疗显著改善了18名7个月以下婴儿型庞贝病患儿的心肌病、通气功能和总生存率。18名患者中有16名进入了一项扩展研究,他们继续接受阿糖苷酶α治疗,每两周一次,剂量为20mg/kg(n = 8)或40mg/kg(n = 8),总共持续3年。这些儿童在36个月大时继续表现出阿糖苷酶α治疗的益处。Cox回归分析显示,在整个研究期间,与未治疗的历史对照组相比,阿糖苷酶α治疗使死亡风险降低了95%,使有创通气或死亡风险降低了91%,使任何类型的通气或死亡风险降低了87%。心肌病持续改善,11名患者学会并维持了显著的运动技能。每两周20mg/kg和40mg/kg剂量之间在安全性或疗效参数方面均未观察到显著差异。总体而言,长期阿糖苷酶α治疗显著延长了生存期以及无通气生存期,并改善了心肌病。