Skeletal Biology and Engineering Research Center, KU Leuven Department of Development and Regeneration, Leuven, Belgium.
Rheumatology, University Hospitals Leuven, Leuven, Belgium.
Scand J Rheumatol. 2022 Nov;51(6):470-480. doi: 10.1080/03009742.2021.1955467. Epub 2021 Sep 13.
In patients with rheumatoid arthritis (RA) in sustained remission, tapering of biological disease-modifying anti-rheumatic drugs can be considered. Tapering has already been investigated, but its feasibility remains to be determined. Therefore, we explored the feasibility of tapering etanercept in RA in a setting close to practice.
Patients with RA in 28-joint Disease Activity Score (DAS28) remission (≥ 6 months) and treated with etanercept 50 mg weekly (≥ 1 year) were included in the pragmatic 1 year open-label multicentre randomized controlled TapERA (Tapering Etanercept in Rheumatoid Arthritis) trial. Patients were assigned to continue etanercept weekly or to taper to every other week (EOW). Patients who lost remission [DAS28-C-reactive protein (CRP) ≥ 2.6] were re-escalated to etanercept weekly. The primary outcome was the proportion of patients maintaining DAS28-CRP remission for 6 months.
Sixty-six patients were randomized to etanercept weekly (n = 34) or EOW (n = 32). After 6 months, 26/34 patients (76%) in the weekly and 19/32 (59%) in the EOW group maintained disease control (p = 0.136). In the EOW group, 20/32 patients (63%) remained on their tapered treatment during the trial. Two patients reintroduced weekly etanercept themselves. Ten patients were re-escalated to etanercept weekly by the rheumatologist, after a median (interquartile range) interval of 3.0 (2.0-6.0) months. Among these patients, 7/10 regained remission after re-escalation, four of them at the next study visit.
Although non-inferiority could not be demonstrated, tapering of etanercept to EOW appeared feasible in patients in sustained remission.
在持续缓解的类风湿关节炎(RA)患者中,可以考虑逐渐减少生物性疾病修饰抗风湿药物(DMARDs)的用量。虽然已经对逐渐减量进行了研究,但仍需要确定其可行性。因此,我们在更接近实际情况的环境中探索了 RA 患者中逐渐减少依那西普的可行性。
纳入在 28 关节疾病活动度评分(DAS28)缓解(≥6 个月)且接受依那西普 50mg 每周(≥1 年)治疗的 RA 患者,进行了一项实用的 1 年开放性标签多中心随机对照 TapERA(类风湿关节炎中依那西普的逐渐减量)试验。患者被分配继续每周接受依那西普治疗或每两周一次(EOW)。失去缓解[DAS28-C 反应蛋白(CRP)≥2.6]的患者重新增加至每周依那西普。主要结局是 6 个月时维持 DAS28-CRP 缓解的患者比例。
66 例患者被随机分配至每周依那西普组(n=34)或 EOW 组(n=32)。6 个月后,每周组 34 例患者中有 26 例(76%)和 EOW 组 32 例患者中有 19 例(59%)维持疾病控制(p=0.136)。在 EOW 组,32 例患者中有 20 例(63%)在试验期间继续接受他们的减量治疗。两名患者自行重新开始每周接受依那西普治疗。10 例患者经风湿病医生评估后重新开始每周接受依那西普治疗,中位(四分位距)时间为 3.0(2.0-6.0)个月。这些患者中有 7 例在重新开始治疗后恢复缓解,其中 4 例在下次研究就诊时缓解。
虽然未能证明非劣效性,但在持续缓解的患者中,将依那西普逐渐减少至 EOW 似乎是可行的。