Department of Rheumatology, Sint Maartenskliniek, Nijmegen, The Netherlands.
Department of Rheumatology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Ann Rheum Dis. 2017 Oct;76(10):1716-1722. doi: 10.1136/annrheumdis-2017-211169. Epub 2017 Jun 12.
Tumour necrosis factor inhibitors (TNFi) are effective in rheumatoid arthritis (RA), but disadvantages include adverse events (AEs) and high costs. This can be improved by disease activity-guided dose reduction (DR). We aimed to assess long-term outcomes of TNFi DR in RA by using 3-year data from the DRESS study (Dose REduction Strategy of Subcutaneous TNF inhibitors study).
In the intervention phase (month 0-18) of the DRESS study (Dutch trial register, NTR 3216), patients were randomised to DR or usual care (UC). In the extension phase (month 18-36), treatment strategies in both groups converged to continuation of protocolised tight control and allowed dose optimisation. Intention-to-treat analyses were done on flare, disease activity (28 joint count-based disease activity score with C reactive protein (DAS28-CRP)), functioning (health assessment questionnaire-disability index (HAQ-DI)), quality of life (Euroqol 5 dimensions 5 levels questionnaire (EQ5D-5L)), medication use, radiographic progression (Sharp van der Heijde score (SvdH)) and AE.
172/180 patients included in the DRESS study were included in the extension phase. Cumulative incidences of major flare were 10% and 12% (-2%, 95% CI -8 to 15) in DR and UC groups in the extension phase, and 17% and 14% (3%, 95% CI -9 to 13) from 0 to 36 months. Cumulative incidences of short-lived flares were 43% (33 to 52%)%) and 35% (23 to 49%)%) in DR and UC groups in the extension phase, and 83% (75 to 90%)%) and 44% (31 to 58%)%) from 0 to 36 months. Mean DAS28-CRP, HAQ-DI, EQ5D-5L and SvdH remained stable and not significantly different between groups. TNFi use remained low in the DR group and decreased in the UC group. Cumulative incidences of AE were not significantly different between groups.
Safety and efficacy of disease activity guided TNFi DR in RA are maintained up to 3 years, with a large reduction in TNFi use, but no other benefits. Implementation of DR would vastly improve the cost-effective use of TNFi.
肿瘤坏死因子抑制剂(TNFi)在类风湿关节炎(RA)中有效,但缺点包括不良事件(AEs)和高成本。通过疾病活动指导的剂量减少(DR)可以改善这种情况。我们旨在通过 DRESS 研究(皮下 TNF 抑制剂剂量减少策略研究)的 3 年数据来评估 RA 中 TNFi DR 的长期结果。
在 DRESS 研究(荷兰试验注册处,NTR 3216)的干预阶段(第 0-18 个月),患者被随机分配到 DR 或常规护理(UC)组。在扩展阶段(第 18-36 个月),两组的治疗策略趋于一致,继续进行协议化的严格控制,并允许剂量优化。对 flares、疾病活动度(基于 28 个关节计数的疾病活动评分与 C 反应蛋白(DAS28-CRP))、功能(健康评估问卷残疾指数(HAQ-DI))、生活质量(欧洲五维健康量表 5 级问卷(EQ5D-5L))、药物使用、放射学进展(Sharp van der Heijde 评分(SvdH))和 AEs 进行意向治疗分析。
172/180 名纳入 DRESS 研究的患者被纳入扩展阶段。DR 和 UC 组在扩展阶段的主要 flares 的累积发生率分别为 10%和 12%(-2%,95%CI-8 至 15),0 至 36 个月时分别为 17%和 14%(3%,95%CI-9 至 13)。DR 和 UC 组在扩展阶段的短暂 flares 的累积发生率分别为 43%(33 至 52%)和 35%(23 至 49%),0 至 36 个月时分别为 83%(75 至 90%)和 44%(31 至 58%)。DAS28-CRP、HAQ-DI、EQ5D-5L 和 SvdH 均值在两组间保持稳定,无显著差异。DR 组 TNFi 的使用率仍然较低,UC 组的使用率则下降。两组的 AEs 累积发生率无显著差异。
在 RA 中,疾病活动指导的 TNFi DR 的安全性和疗效可维持 3 年,TNFi 的使用量大幅减少,但无其他益处。实施 DR 将极大地改善 TNFi 的成本效益利用。