Lubrano Ennio, Parsons Wendy J, Perrotta Fabio Massimo
From the Academic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio," University of Molise, Campobasso, Italy.E. Lubrano, MD, PhD, Academic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio," University of Molise; W.J. Parsons, BSc, MPH, Academic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio," University of Molise; F.M. Perrotta, MD, Academic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio," University of Molise.
J Rheumatol. 2016 May;43(5):918-23. doi: 10.3899/jrheum.151404. Epub 2016 Mar 15.
To assess the response to treatment, remission, and minimal disease activity (MDA) in a group of patients with predominant axial psoriatic arthritis (axPsA). Predictors of response were also evaluated.
Patients fulfilling the ClASsification of Psoriatic ARthritis (CASPAR) criteria and treated with anti-tumor necrosis factor (anti-TNF) agents adalimumab, etanercept, and golimumab were enrolled and prospectively followed every 4 months for 1 year in a clinical practice setting. Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) 50 was assessed as a set of response criteria to treatment; Composite Psoriatic Disease Activity Index (CPDAI) < 4, Disease Activity Index for Psoriatic Arthritis (DAPSA) score ≤ 3.3, and partial remission (PR) were also evaluated as remission criteria. Patients were considered in MDA when they met at least 5/7 of the criteria previously defined. Patients achieving BASDAI 50, PR, and MDA were compared to identify outcome predictor factors. Concordance between the outcome measures was also performed.
Of the 58 patients treated with anti-TNF, at baseline no patients were in PR or MDA. No patients had a CPDAI < 4 or a DAPSA score ≤ 3.3. After 12 months, BASDAI 50 was achieved in 15/48 patients (31.2%). CPDAI < 4, DAPSA score ≤ 3.3, PR, and MDA were achieved, respectively, in 17/48 (35.4%), 11/48 (22.9%), 11/48 (22.9%), and 24/48 (50%) patients. No difference was found among the 3 anti-TNF. Predictors for MDA were male sex, young age, low disease duration, low Health Assessment Questionnaire score, and absence of enthesitis.
This longitudinal observational study, based on a clinical practice setting, showed that remission and MDA are achievable targets in axPsA treated with anti-TNF. Predictors of remission and MDA were also identified.
评估一组以中轴型银屑病关节炎(axPsA)为主的患者对治疗的反应、缓解情况及最小疾病活动度(MDA)。还对反应的预测因素进行了评估。
纳入符合银屑病关节炎分类标准(CASPAR)且接受抗肿瘤坏死因子(抗TNF)药物阿达木单抗、依那西普和戈利木单抗治疗的患者,并在临床实践环境中每4个月进行一次前瞻性随访,为期1年。将巴斯强直性脊柱炎疾病活动指数(BASDAI)改善50%作为一组治疗反应标准进行评估;复合银屑病疾病活动指数(CPDAI)<4、银屑病关节炎疾病活动指数(DAPSA)评分≤3.3以及部分缓解(PR)也作为缓解标准进行评估。当患者至少符合先前定义的7项标准中的5项时,即被视为处于最小疾病活动度状态。对达到BASDAI改善50%、PR和MDA的患者进行比较,以确定结局预测因素。还对结局指标之间的一致性进行了分析。
在58例接受抗TNF治疗的患者中,基线时无患者处于部分缓解或最小疾病活动度状态。没有患者的CPDAI<4或DAPSA评分≤3.3。12个月后,48例患者中有15例(31.2%)达到BASDAI改善50%。48例患者中分别有17例(35.4%)、11例(22.9%)、11例(22.9%)和24例(50%)达到CPDAI<4、DAPSA评分≤3.3、部分缓解和最小疾病活动度状态。三种抗TNF药物之间未发现差异。最小疾病活动度的预测因素为男性、年龄较小、病程较短、健康评估问卷评分较低以及无附着点炎。
这项基于临床实践环境的纵向观察性研究表明,在接受抗TNF治疗的axPsA患者中,缓解和最小疾病活动度是可以实现的目标。还确定了缓解和最小疾病活动度的预测因素。