Baraliakos X, Brandt J, Listing J, Haibel H, Sörensen H, Rudwaleit M, Sieper J, Braun J
Rheumazentrum Ruhrgebiet, Herne, Ruhr-University Bochum, Bochum, Germany.
Arthritis Rheum. 2005 Dec 15;53(6):856-63. doi: 10.1002/art.21588.
To examine the long-term outcome of patients with active ankylosing spondylitis (AS) clinically and by magnetic resonance imaging (MRI) after continuous treatment with the tumor necrosis factor (TNF) receptor fusion protein etanercept over 2 years.
Overall, 26 patients with active AS were treated with etanercept 25 mg twice daily subcutaneously, twice weekly with no concomitant disease-modifying antirheumatic drugs (DMARDs) or steroids. The clinical response was assessed by standardized parameters. Inflammatory spinal lesions were quantified by the ASspiMRI-a rating gadolinium-enhanced (T1-weighted gadolinium diethylenetriaminepentaacetic acid) and STIR MRI sequences. The primary outcome was a Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) improvement > or =50% after 2 years of etanercept therapy compared with the baseline value of the study.
Overall, 21 (70%) of 30 patients completed year 2. In the intent-to-treat analysis, 54% of the patients showed a 50% improvement according to the BASDAI and a 40% improvement according to the Assessment in Ankylosing Spondylitis (ASAS) criteria. In the completer analysis, 9 (43%) of 21 patients were in partial remission according to ASAS criteria. Mean +/- SD BASDAI scores, which were elevated at baseline (6.3 +/- 1.6), remained low: 2.7 +/- 2.4 after 2 years compared with 2.6 +/- 2.2 at week 54. In accordance, all other clinical parameters showed sustained improvement during year 2. The majority of patients had no disease activity flares. MRI evaluation showed a 75% improvement of active spinal lesions, but minor spinal inflammation was still present in 64% of the patients after 2 years. There were 2 serious adverse events leading to discontinuation of etanercept.
The clinical efficacy and safety of etanercept in patients with active AS without simultaneous administration of DMARDs or steroids over 2 years of continuous treatment is confirmed. Spinal inflammation as depicted by MRI decreased significantly, but a few patients still had some spinal inflammation even after long-term anti-TNF therapy.
通过临床及磁共振成像(MRI)检查,评估肿瘤坏死因子(TNF)受体融合蛋白依那西普连续治疗2年以上的活动性强直性脊柱炎(AS)患者的长期疗效。
总共26例活动性AS患者接受皮下注射依那西普25mg,每日两次,每周两次,未同时使用改善病情抗风湿药(DMARDs)或类固醇。通过标准化参数评估临床反应。采用ASspiMRI-a评分钆增强(T1加权钆二乙三胺五乙酸)和短T1反转恢复(STIR)MRI序列对脊柱炎性病变进行量化。主要结局是与研究基线值相比,依那西普治疗2年后巴斯强直性脊柱炎疾病活动指数(BASDAI)改善≥50%。
总共30例患者中有21例(70%)完成了2年治疗。在意向性分析中,54%的患者根据BASDAI显示改善50%,根据强直性脊柱炎评估(ASAS)标准显示改善40%。在完成治疗分析中,21例患者中有9例(43%)根据ASAS标准达到部分缓解。平均±标准差BASDAI评分在基线时升高(6.3±1.6),2年后仍保持较低水平:2.7±2.4,而在第54周时为2.6±2.2。相应地,所有其他临床参数在第2年期间均持续改善。大多数患者没有疾病活动复发。MRI评估显示活动性脊柱病变改善75%,但2年后仍有64%的患者存在轻微脊柱炎症。有2例严重不良事件导致依那西普停药。
证实了依那西普在未同时使用DMARDs或类固醇的活动性AS患者中连续治疗2年的临床疗效和安全性。MRI显示的脊柱炎症显著减少,但即使经过长期抗TNF治疗,仍有少数患者存在一些脊柱炎症。