Bristol Eye Hospital, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom.
Clinical Trials Research Centre, Department of Biostatistics, University of Liverpool, Liverpool, United Kingdom.
Am J Ophthalmol. 2019 Nov;207:170-174. doi: 10.1016/j.ajo.2019.06.007. Epub 2019 Jun 13.
To determine longer-term outcomes of participants enrolled from a single center in the SYCAMORE trial, a randomized placebo-controlled trial of adalimumab vs placebo in children with juvenile idiopathic arthritis-associated uveitis (JIA-U) uncontrolled on methotrexate.
Retrospective interventional case series.
Medical records of all 28 SYCAMORE participants recruited at the Bristol Eye Hospital were reviewed at approximately 3-monthly intervals up to 5 years from the trial randomization date. Uveitis activity, treatment course, visual outcomes, ocular complications, and adverse events were recorded. Data are presented using summary statistics.
Following withdrawal of the investigational medicinal product (IMP), 25 of the 28 participants were started on adalimumab for active JIA-U. Of the 12 participants in the active treatment arm of the SYCAMORE study, 11 (92%) were restarted on adalimumab after withdrawal of the IMP for active JIA-U (median time to flare 188 days [range 42-413 days). Two participants stopped adalimumab for uncontrolled JIA-U. One participant had a reduction in vision to 0.3 owing to cataract. Mean visual acuity for the remaining 27 participants was -0.04 (right eye) and -0.05 (left eye).
Drug-induced remission of JIA-U did not persist when adalimumab was withdrawn after 1-2 years of treatment. Adalimumab was well tolerated and visual acuity outcomes were excellent.
确定 SYCAMORE 试验中单一中心入组参与者的长期结局,该试验为接受甲氨蝶呤治疗但未控制的幼年特发性关节炎相关葡萄膜炎(JIA-U)患儿中阿达木单抗与安慰剂的随机安慰剂对照试验。
回顾性干预性病例系列研究。
对布里斯托眼医院招募的 28 名 SYCAMORE 参与者的医疗记录进行了回顾,随访时间约为从试验随机分组日期起 5 年,每 3 个月一次。记录葡萄膜炎活动、治疗过程、视力结果、眼部并发症和不良事件。使用汇总统计数据报告数据。
在停用研究用药物(IMP)后,28 名参与者中的 25 名因活动性 JIA-U 开始接受阿达木单抗治疗。在 SYCAMORE 研究的活性治疗组的 12 名参与者中,11 名(92%)在 IMP 停止后因活动性 JIA-U 重新开始接受阿达木单抗治疗(中位复发时间为 188 天[范围 42-413 天)。两名参与者因未控制的 JIA-U 停止使用阿达木单抗。一名参与者因白内障导致视力下降至 0.3。其余 27 名参与者的平均视力为-0.04(右眼)和-0.05(左眼)。
在接受 1-2 年治疗后停用阿达木单抗时,JIA-U 的药物诱导缓解并未持续。阿达木单抗耐受性良好,视力结果极佳。