Soubrier Martin, Pereira Bruno, Frayssac Thomas, Abdi Dihya, Couderc Marion, Daron Coline, Malochet-Guinamand Sandrine, Mathieu Sylvain, Tatar Zuzana, Tournadre Anne, Dubost Jean-Jacques
Department of Rheumatology, CHU Hôpital Gabriel Montpied, Clermont-Ferrand, France.
Biostatistics and Research Department (DRCI), CHU Hôpital Gabriel Montpied, Clermont-Ferrand, France.
Clin Exp Rheumatol. 2016 Nov-Dec;34(6):1059-1064. Epub 2016 Aug 31.
While several registries have already evaluated the retention of anti-TNF therapy in psoriatic arthritis (PsA), they sometimes reach divergent conclusions. Our study therefore sought to assess therapeutic retention rates and predictive factors of response in a patient cohort from Auvergne, France, followed up in routine clinical practice.
Medical records of all PsA patients treated from 2002 to May 2015 were analysed. PsA diagnosis was established based on the CASPAR criteria.
In total, 102 patients were analysed, comprising 62 men (44.6±12.6 years) and 40 women (37.8±13.4). Mean PsA evolution was 2.7 years (0.8-11.2). The most common forms were peripheral (47/102, 45.1%) and mixed (46/102, 46.1%) PsA. The anti-TNF treatment initiated was etanercept in 47 cases (45.2%), adalimumab in 29 (27.9%), infliximab in 20 (19.2%), and golimumab in six [5.8%]. In 28 cases (27.4%), anti-TNF was associated with methotrexate (MTX). Overall, the median duration of anti-TNF retention was 76.5 months. The hazard ratios (HR) for treatment cessation did not significantly differ between the etanercept and monoclonal antibody groups (HR=1.35[0.96-1.93], p=0.08). After 5 years, approximately 30.8% of etanercept patients and 68.8% of monoclonal antibody patients (adalimumab 71.2%; infliximab 67.2%) were still being treated. Combining with MTX did not prolong the overall retention rate (HR=0.85[0.37-1.96], p=0.71). Tobacco use was predictive of discontinuation (p=0.03).
Our study demonstrates good anti-TNF treatment retention in PsA patients, as well as confirming the deleterious effect of smoking while providing no argument in favour of combined treatment with MTX to improve maintenance.
虽然已有多个登记处评估了银屑病关节炎(PsA)患者抗TNF治疗的持续率,但有时会得出不同的结论。因此,我们的研究旨在评估法国奥弗涅地区一组在常规临床实践中接受随访的PsA患者的治疗持续率及反应预测因素。
分析了2002年至2015年5月期间所有接受治疗的PsA患者的病历。PsA诊断依据CASPAR标准确定。
共分析了102例患者,其中男性62例(44.6±12.6岁),女性40例(37.8±13.4岁)。PsA的平均病程为2.7年(0.8 - 11.2年)。最常见的类型是外周型(47/102,45.1%)和混合型(46/102,46.1%)PsA。起始的抗TNF治疗中,47例(45.2%)使用依那西普,29例(27.9%)使用阿达木单抗,20例(19.2%)使用英夫利昔单抗,6例(5.8%)使用戈利木单抗。28例(27.4%)患者中,抗TNF与甲氨蝶呤(MTX)联合使用。总体而言,抗TNF治疗的中位持续时间为76.5个月。依那西普组和单克隆抗体组的治疗终止风险比(HR)无显著差异(HR = 1.35[0.96 - 1.93],p = 0.08)。5年后,约30.8%的依那西普患者和68.8%的单克隆抗体患者(阿达木单抗71.2%;英夫利昔单抗67.2%)仍在接受治疗。与MTX联合使用并未延长总体持续率(HR = 0.85[0.37 - 1.96],p = 0.71)。吸烟是停药的预测因素(p = 0.03)。
我们的研究表明PsA患者抗TNF治疗的持续率良好,同时证实了吸烟的有害影响,且未发现支持与MTX联合治疗以改善维持治疗效果的依据。