Division of Rheumatology, The Hospital for Sick Children, University of Toronto, Canada, and German Center for Paediatric and Adolescent Rheumatology, Garmisch-Partenkirchen, Germany.
Clin Exp Rheumatol. 2014 May-Jun;32(3):424-31. Epub 2014 Jan 3.
A significant proportion of patients with juvenile spondyloarthritis (JSpA) are refractory to treatment with established medications. The objective of this study was to assess long-term efficacy of treatment with anti-TNF agents in patients with JSpA.
An observational study of 16 patients with JSpA from 3 centres treated with infliximab (n=10) and etanercept (n=6) was performed, with a median follow-up period of 7.2 years. Prospective data was collected according to a standardized protocol. Outcomes examined were TEC, TAJC, markers of inflammation (ESR, CRP), functional assessments (C-HAQ, BASDAI, BASFI), and ongoing requirement for anti-TNF treatment.
13/16 patients (83%) had achieved clinical remission 6 months into the treatment. Improvement was sustained over time, with a median TAJC and TEC of 0 at any time point after 6 weeks. 6/16 patients (38%) showed a flare of arthritis after a median of 3.5 years. Two patients with hip disease prior to treatment required an arthroplasty 3 and 8 years post anti-TNF initiation. Patients showed progression of sacroiliitis with median modified New York score of 1 (range 0-3) at time of diagnosis and 3 (range 0-4) at last follow-up (p=0.002). Median BASDAI at last follow up was 1.6, median BASFI 3.1. Two patients developed transient reactions (one generalised, one local); no patient developed other adverse effects during the study.
Anti-TNF treatment in JSpA refractory to standard treatment results in good long-term disease control except for pre-existing hip disease. However, radiographic evidence suggests inferior efficacy for control of sacroiliac joint disease.
相当一部分幼年特发性关节炎(JSpA)患者对现有药物治疗无反应。本研究旨在评估抗 TNF 药物治疗 JSpA 患者的长期疗效。
对来自 3 个中心的 16 例 JSpA 患者(10 例使用英夫利昔单抗,6 例使用依那西普)进行了观察性研究,中位随访时间为 7.2 年。根据标准化方案收集前瞻性数据。评估的结局包括 TJC、SJC、炎症标志物(ESR、CRP)、功能评估(C-HAQ、BASDAI、BASFI)和持续抗 TNF 治疗的需求。
16 例患者中有 13 例(83%)在治疗 6 个月时达到临床缓解。随着时间的推移,改善持续存在,在 6 周后任何时间点的 TJC 和 TEC 中位数均为 0。16 例患者中有 6 例(38%)在中位时间 3.5 年后出现关节炎发作。2 例治疗前髋关节疾病患者在抗 TNF 治疗后 3 年和 8 年分别进行了关节置换术。患者的骶髂关节炎进展,诊断时改良纽约评分中位数为 1(范围 0-3),末次随访时为 3(范围 0-4)(p=0.002)。末次随访时 BASDAI 中位数为 1.6,BASFI 中位数为 3.1。2 例患者出现短暂反应(1 例全身性,1 例局部性);在研究期间,没有患者出现其他不良反应。
在标准治疗无效的 JSpA 患者中使用抗 TNF 治疗可获得良好的长期疾病控制,但对于存在的髋关节疾病除外。然而,影像学证据表明,控制骶髂关节疾病的疗效较差。