Fransen J, Antoni C, Mease P J, Uter W, Kavanaugh A, Kalden J R, Van Riel P L C M
Department of Rheumatology, Radboud University Nijmegen Medical Centre, PO Box 9101, NL-6500HB Nijmegen, The Netherlands.
Ann Rheum Dis. 2006 Oct;65(10):1373-8. doi: 10.1136/ard.2006.051706. Epub 2006 Apr 27.
In recent clinical trials in patients with psoriatic arthritis (PsA), the response criteria and disease activity measures that have been used were those developed for rheumatoid arthritis. However, these have not yet been validated in PsA.
To compare the responsiveness and discriminative capacity of the psoriatic arthritis response criteria (PsARC), American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) response criteria and the Disease Activity Score (DAS) and core-set measures in patients with PsA and peripheral arthritis, using the data from two randomised placebo-controlled trials of tumour necrosis factor inhibitors.
In an infliximab trial, 104 patients with active PsA were randomised to receive placebo or infliximab for 16 weeks. In an etanercept trial, 60 patients with active PsA were randomised to receive placebo or etanercept for 12 weeks. Data from baseline and the end of the intervention phase were used from each study. Responsiveness was assessed using the standardised response mean and effect size. Capacity to discriminate between the active drug and placebo was assessed using t values or a chi2 test. Measures were ranked in order of their t value or chi2 value.
The EULAR criteria performed better in discriminating the active drug from placebo than the ACR20 improvement criteria, which in turn performed better than the PsARC. It was also found that the pooled indices (DAS and DAS28) were generally more responsive, and performed better in discriminating active drug from placebo, than the single core-set measures.
Response criteria and pooled indices developed for rheumatoid arthritis are useful for the assessment of arthritis in PsA clinical trials.
在近期针对银屑病关节炎(PsA)患者的临床试验中,所使用的反应标准和疾病活动度测量方法是针对类风湿关节炎制定的。然而,这些标准尚未在PsA中得到验证。
利用两项肿瘤坏死因子抑制剂随机安慰剂对照试验的数据,比较银屑病关节炎反应标准(PsARC)、美国风湿病学会(ACR)和欧洲抗风湿病联盟(EULAR)反应标准以及疾病活动评分(DAS)和核心指标测量方法在PsA合并外周关节炎患者中的反应性和鉴别能力。
在一项英夫利昔单抗试验中,104例活动期PsA患者被随机分为接受安慰剂或英夫利昔单抗治疗16周。在一项依那西普试验中,60例活动期PsA患者被随机分为接受安慰剂或依那西普治疗12周。每项研究均使用基线和干预阶段结束时的数据。使用标准化反应均值和效应量评估反应性。使用t值或卡方检验评估区分活性药物和安慰剂的能力。根据t值或卡方值对测量方法进行排序。
EULAR标准在区分活性药物和安慰剂方面比ACR20改善标准表现更好,而ACR20改善标准又比PsARC表现更好。还发现,汇总指标(DAS和DAS28)通常比单一核心指标测量方法更具反应性,并且在区分活性药物和安慰剂方面表现更好。
为类风湿关节炎制定的反应标准和汇总指标可用于PsA临床试验中关节炎评估。