Smith Janine A, Thompson Darby J S, Whitcup Scott M, Suhler Eric, Clarke Grace, Smith Susan, Robinson Michael, Kim Jonghyeon, Barron Karyl S
National Eye Institute, NIH, Bethesda, Maryland, USA.
Arthritis Rheum. 2005 Feb 15;53(1):18-23. doi: 10.1002/art.20904.
To investigate the safety and efficacy of etanercept in the treatment of uveitis associated with juvenile idiopathic arthritis (JIA).
Children who met the American College of Rheumatology diagnostic criteria for JIA with active uveitis, who had anterior chamber cells of >/=1+ or requiring topical corticosteroid >/=3 times daily, and who were on a stable regimen for arthritis treatment were eligible. Study participants received etanercept (0.4 mg/kg) or placebo administered subcutaneously twice weekly for 6 months. All participants received open-label etanercept for an additional 6 months.
Five patients received placebo and 7 received etanercept. Three of the 7 patients treated with etanercept and 2 of the 5 placebo-treated patients were considered ophthalmic successes (P = 1.0). One patient in each treatment group was considered a treatment failure. Three of the 7 etanercept-treated and 2 of the 5 placebo-treated patients were neither successes nor failures by our definition. There were no serious adverse events for any patient during the entire study period. Reports of minor infections were comparable in each treatment group, 71% for etanercept and 60% for placebo (P = 0.58).
In this small pilot study there was no apparent difference in the anterior segment inflammation between patients treated with etanercept and placebo. The stringent criteria used to measure ophthalmic success of treatment and the small patient population limit the implications of our findings.
探讨依那西普治疗与青少年特发性关节炎(JIA)相关的葡萄膜炎的安全性和有效性。
符合美国风湿病学会JIA诊断标准且患有活动性葡萄膜炎、前房细胞≥1+或每日需要局部使用糖皮质激素≥3次、且关节炎治疗方案稳定的儿童符合入选条件。研究参与者接受依那西普(0.4mg/kg)或安慰剂皮下注射,每周两次,共6个月。所有参与者再接受开放标签的依那西普治疗6个月。
5名患者接受安慰剂,7名患者接受依那西普治疗。接受依那西普治疗的7名患者中有3名以及接受安慰剂治疗的5名患者中有2名被认为眼科治疗成功(P = 1.0)。每个治疗组各有1名患者被认为治疗失败。按照我们的定义,接受依那西普治疗的7名患者中有3名、接受安慰剂治疗的5名患者中有2名既未成功也未失败。在整个研究期间,任何患者均未发生严重不良事件。每个治疗组轻微感染的报告发生率相当,依那西普组为71%,安慰剂组为60%(P = 0.58)。
在这项小型试点研究中,接受依那西普和安慰剂治疗的患者在前节炎症方面没有明显差异。用于衡量治疗眼科成功的严格标准以及患者数量少限制了我们研究结果的意义。