Department of Rheumatology, Clinical Research Center for Rheumatic Diseases, NHO Kumamoto Saishunsou National Hospital, Kohshi, Kumamoto, 861-1196, Japan.
Rheumatic and Collagen Disease Center, Sasebo Chuo Hospital, Sasebo, Nagasaki, 857-1195, Japan.
Clin Rheumatol. 2019 Dec;38(12):3391-3400. doi: 10.1007/s10067-019-04721-z. Epub 2019 Aug 9.
This study was designed to compare outcomes of dose reduction, withdrawal, and continuation of tofacitinib in patients with rheumatoid arthritis (RA) and to examine effectiveness of rescue with an original treatment regimen for disease flare.
We prospectively enrolled 100 patients who had high or moderate disease activity and treated them with tofacitinib at 5 mg twice daily for 1 year. All patients achieving remission or low disease activity (LDA) were assigned to a withdrawal, dose-reduction, or continuation group, then followed until disease flare or end of the study. For flare cases, the original treatment regimen was reintroduced.
During the first year, 68 patients achieved remission or LDA (median sustained time 49.0 weeks). Subsequently, disease flare occurred at the following crude incidence rates per person-year (95% confidence interval [CI]): 0.73 (0.43-1.22) after withdrawal, 0.44 (0.25-0.77) after dose reduction, and 0.04 (0.01-0.27) during continuation. Kaplan-Meier estimates of median flare-free time (95% CI) were 7.0 months (2.8-11.2) for withdrawal and 21.0 months (4.1-37.9) for dose reduction. In the Cox regression analysis, adjusted hazard ratios (95% CIs) were 18.11 (2.38-138) for withdrawal and 9.13 (1.19-70.4) for dose reduction compared with continuation. Restart of the original treatment regimen led to rapid remission in flare cases (93% for withdrawal and 100% for dose reduction).
After achievement of remission or LDA, the dose-reduction strategy seems preferable to immediate withdrawal of tofacitinib. Restart of the original regimen can reinduce RA control in flare cases.Key Points• During the 1-year tofacitinib therapy, two-thirds of RA patients with high or moderate disease activity achieved rapid and sustained remission or low disease activity.• During subsequent years, the incidence rate and adjusted hazard ratio for disease flare were significantly higher following tofacitinib immediate withdrawal than following dose reduction.• Half of the patients were estimated to remain flare-free for 21 months after dose reduction and for 7 months after withdrawal of tofacitinib.• Restart of the original treatment regimen rapidly restored disease control in almost all flare cases.
本研究旨在比较类风湿关节炎(RA)患者接受托法替布剂量减少、停药和继续治疗的结局,并探讨对疾病复发采用原治疗方案进行挽救治疗的效果。
我们前瞻性纳入了 100 例高疾病活动度或中疾病活动度的患者,给予托法替布 5mg,每日 2 次,治疗 1 年。所有达到缓解或低疾病活动度(LDA)的患者被分配到停药、剂量减少或继续治疗组,然后继续随访,直至疾病复发或研究结束。对于复发的患者,重新采用原治疗方案。
在第 1 年,68 例患者达到缓解或 LDA(中位持续时间 49.0 周)。随后,复发的粗发生率(人年)分别为:停药后 0.73(0.43-1.22)、剂量减少后 0.44(0.25-0.77)、继续治疗后 0.04(0.01-0.27)。Kaplan-Meier 估计的无复发中位时间(95%CI)分别为:停药后 7.0 个月(2.8-11.2)、剂量减少后 21.0 个月(4.1-37.9)。Cox 回归分析显示,与继续治疗相比,调整后的危险比(95%CI)分别为 18.11(2.38-138)和 9.13(1.19-70.4)。复发后重新采用原治疗方案可迅速缓解 RA(停药后 93%,剂量减少后 100%)。
在达到缓解或 LDA 后,减少剂量的策略似乎优于立即停用托法替布。在复发的情况下,重新采用原方案可重新诱导 RA 缓解。
在托法替布 1 年治疗期间,三分之二的高疾病活动度或中疾病活动度的 RA 患者迅速且持续地达到缓解或低疾病活动度。
在随后的几年中,托法替布立即停药后的疾病复发发生率和调整后的危险比显著高于剂量减少后。
一半的患者估计在剂量减少后可无复发地维持 21 个月,停药后可维持 7 个月。
在几乎所有复发患者中,重新采用原治疗方案可迅速恢复疾病控制。