Goodman A D, Rossman H, Bar-Or A, Miller A, Miller D H, Schmierer K, Lublin F, Khan O, Bormann N M, Yang M, Panzara M A, Sandrock A W
Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Neurology. 2009 Mar 3;72(9):806-12. doi: 10.1212/01.wnl.0000343880.13764.69.
To evaluate the safety and tolerability of natalizumab when added to glatiramer acetate (GA) in patients with relapsing multiple sclerosis. The primary outcome assessed whether this combination would increase the rate of development of new active lesions on cranial MRI scans vs GA alone.
This phase 2, randomized, double-blind, placebo-controlled study included patients aged 19 to 55 years who were treated with GA for at least 1 year before randomization and experienced at least one relapse during the previous year. Patients received IV natalizumab 300 mg (n = 55) or placebo (n = 55) once every 4 weeks plus GA 20 mg subcutaneously once daily for < or = 20 weeks.
The mean rate of development of new active lesions was 0.03 with combination therapy vs 0.11 with GA alone (p = 0.031). Combination therapy resulted in lower mean numbers of new gadolinium-enhancing lesions (0.6 vs 2.3 for GA alone, p = 0.020) and new/newly enlarging T2-hyperintense lesions (0.5 vs 1.3, p = 0.029). The incidence of infection and infusion reactions was similar in both groups; no hypersensitivity reactions were observed. One serious adverse event occurred with combination therapy (elective hip surgery). With the exception of an increase in anti-natalizumab antibodies with combination therapy, laboratory data were consistent with previous clinical studies of natalizumab alone.
The combination of natalizumab and glatiramer acetate seemed safe and well tolerated during 6 months of therapy.
评估在复发型多发性硬化症患者中,将那他珠单抗添加到醋酸格拉替雷(GA)治疗方案中的安全性和耐受性。主要结局指标是评估这种联合治疗与单独使用GA相比,是否会增加头颅磁共振成像(MRI)扫描上新发活动性病灶的发生率。
这项2期随机双盲安慰剂对照研究纳入了年龄在19至55岁之间的患者,这些患者在随机分组前接受GA治疗至少1年,且在前一年至少经历过一次复发。患者每4周接受一次静脉注射那他珠单抗300mg(n = 55)或安慰剂(n = 55),同时每天皮下注射GA 20mg,持续≤20周。
联合治疗组新发活动性病灶的平均发生率为0.03,而单独使用GA组为0.11(p = 0.031)。联合治疗导致新钆增强病灶的平均数量更低(单独使用GA组为2.3,联合治疗组为0.6,p = 0.020)以及新的/新增大的T2高信号病灶数量更低(单独使用GA组为1.3,联合治疗组为0.5,p = 0.029)。两组感染和输液反应的发生率相似;未观察到过敏反应。联合治疗发生了1例严重不良事件(择期髋关节手术)。除联合治疗组抗那他珠单抗抗体增加外,实验室数据与之前单独使用那他珠单抗的临床研究一致。
在6个月的治疗期间,那他珠单抗与醋酸格拉替雷联合使用似乎安全且耐受性良好。