Noseworthy J H, O'Brien P, Erickson B J, Lee D, Sneve D, Ebers G C, Rice G P, Auty A, Hader W J, Kirk A, Duquette P, Carter J, Francis G, Metz L, Shuster E
Mayo Clinic/Mayo Foundation, Rochester, MN 55905, USA.
Neurology. 1998 Nov;51(5):1342-52. doi: 10.1212/wnl.51.5.1342.
To determine whether sulfasalazine is better than placebo in slowing disability progression in MS.
In this randomized, double-blind, placebo-controlled phase III trial, 199 patients with active relapsing-remitting (n = 151) or progressive (n = 48) MS were evaluated at 3-month intervals for a minimum of 3 years (94% completed 3 years of follow-up; mean follow-up, 3.7 years). MRI studies were performed at 6-month intervals on a subset of 89 patients.
Sulfasalazine failed to slow or prevent disability progression as measured by the primary outcome (confirmed worsening of the Expanded Disability Status Scale [EDSS] score by at least 1.0 point on two consecutive 3-month visits). Sulfasalazine influenced favorably a number of secondary outcomes during the first 18 months of the trial (e.g., annualized relapse rate, proportion of relapse-free patients; progressive subgroup only: rate of EDSS progression at 1 and 2 years, median time to EDSS progression) but these positive findings were not sustained into the second half of the trial.
Sulfasalazine does not prevent EDSS score progression in the subset of MS patients studied by this protocol. Treatments may improve relapse-related outcomes in MS, at least temporarily, without providing sustained slowing of EDSS progression. Phase III MS trials should be of sufficient length to determine a meaningful impact on disease course.
确定柳氮磺胺吡啶在延缓多发性硬化症(MS)患者残疾进展方面是否优于安慰剂。
在这项随机、双盲、安慰剂对照的III期试验中,每3个月对199例复发缓解型(n = 151)或进展型(n = 48)MS患者进行评估,为期至少3年(94%完成3年随访;平均随访3.7年)。对89例患者亚组每6个月进行一次MRI检查。
以主要结局指标(连续两次3个月访视时确认扩展残疾状态量表[EDSS]评分恶化至少1.0分)衡量,柳氮磺胺吡啶未能延缓或预防残疾进展。在试验的前18个月,柳氮磺胺吡啶对一些次要结局有有利影响(如年化复发率、无复发患者比例;仅进展型亚组:1年和2年时EDSS进展率、EDSS进展的中位时间),但这些阳性结果在试验后半段未持续。
在本方案研究的MS患者亚组中,柳氮磺胺吡啶不能预防EDSS评分进展。治疗可能至少暂时改善MS中与复发相关的结局,而不会持续延缓EDSS进展。III期MS试验应有足够长的时间来确定对疾病进程的有意义影响。