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所有的 JAK 抑制剂在治疗类风湿关节炎方面都等效吗?托法替布、巴瑞替尼、乌帕替尼和费乐替尼疗效的调整间接比较。

Are all JAK inhibitors for the treatment of rheumatoid arthritis equivalent? An adjusted indirect comparison of the efficacy of tofacitinib, baricitinib, upadacitinib, and filgotinib.

机构信息

Pharmacy Department, Hospital de la Santa Creu i Sant Pau (HSCSP), 08025, Barcelona, Spain.

Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), 08041, Barcelona, Spain.

出版信息

Clin Rheumatol. 2023 Dec;42(12):3225-3235. doi: 10.1007/s10067-023-06787-2. Epub 2023 Oct 13.

Abstract

INTRODUCTION

Comparisons of Janus kinase inhibitors (JAKi) for treatment of rheumatoid arthritis in patients with inadequate response to biologic disease-modifying anti-rheumatic drugs are lacking. We assessed the relative efficacy and safety of four JAKi (tofacitinib, baricitinib, upadacitinib, and filgotinib) in this context.

METHOD

We performed an adjusted indirect comparison (IC) of randomized clinical trials using Bucher's method with an IC and mixed calculator. Endpoints were Disease Activity Score C-reactive protein (DAS28-CRP) and American College of Rheumatology-20 (ACR20). Equivalence was assessed using the equivalent therapeutic alternatives (ETA) guidelines.

RESULTS

We included four of 133 potentially relevant studies. IC showed no statistically significant differences between the four JAKi regarding DAS28-CRP < 3.2. Results were similar in terms of ACR20 except for tofacitinib showing lower efficacy than upadacitinib (RAR -18.4% [IC95% -33.4 to -3.5], p=0.0157). Statistically significant differences were related to the relevant difference for tofacitinib in both endpoints. Despite no statistical differences for baricitinib, we observed a probably clinically relevant difference regarding DAS28-CRP. Probably clinically relevant differences were found for tofacitinib vs. upadacitinib in both endpoints, and for baricitinib vs. upadacitinib in DAS28-CRP. Safety, drug-drug interactions, and convenience considerations did not modify the result of therapeutic equivalence assessment based on efficacy data.

CONCLUSIONS

In conclusion, our results show that filgotinib and upadacitinib are ETA. Baricitinib and upadacitinib are also ETA due to a lack of clear differences and for showing superiority over placebo. The results for tofacitinib and upadacitinib show some inconsistency and more data are needed. Key Points • To date, neither a head-to-head comparison nor an indirect comparison between the Janus kinase inhibitors has been performed in patients with rheumatoid arthritis and an inadequate response to biologic disease-modifying anti-rheumatic drugs. • We performed an adjusted indirect comparison that included randomized clinical trials of tofacitinib, baricitinib, upadacitinib, and filgotinib to assess their equivalence in this scenario. • Our results show that baricitinib and filgotinib are equivalent therapeutic alternatives compared to upadacitinib. However, there is some inconsistency in the results of tofacitinib in front of upadacitinib.

摘要

简介

在生物制剂改善病情的抗风湿药物治疗反应不足的类风湿关节炎患者中,缺乏比较 Janus 激酶抑制剂(JAKi)治疗效果的研究。我们评估了四种 JAKi(托法替布、巴瑞替尼、乌帕替尼和菲戈替尼)在此情况下的相对疗效和安全性。

方法

我们使用 Bucher 法和 IC 和混合计算器进行调整后的间接比较(IC),纳入随机临床试验。终点为疾病活动度评分(DAS28-CRP)和美国风湿病学会 20 项(ACR20)。使用等效治疗替代物(ETA)指南评估等效性。

结果

我们纳入了 133 项潜在相关研究中的 4 项。IC 结果显示,在 DAS28-CRP<3.2 方面,四种 JAKi 之间无统计学差异。ACR20 结果相似,但托法替布的疗效低于乌帕替尼(RAR-18.4%[IC95%-33.4 至-3.5],p=0.0157)。尽管巴瑞替尼无统计学差异,但我们观察到在两个终点均与托法替布相关的临床显著差异。托法替布与乌帕替尼在两个终点,以及巴瑞替尼与乌帕替尼在 DAS28-CRP 方面,均存在可能的临床相关差异。安全性、药物相互作用和便利性考虑均未改变基于疗效数据的治疗等效性评估结果。

结论

总之,我们的结果表明,菲戈替尼和乌帕替尼是 ETA。巴瑞替尼和乌帕替尼也是 ETA,因为缺乏明显差异且优于安慰剂。托法替布和乌帕替尼的结果存在一些不一致,需要更多的数据。关键点:

  • 到目前为止,在生物制剂改善病情的抗风湿药物治疗反应不足的类风湿关节炎患者中,尚未进行过 JAKi 之间的头对头比较或间接比较。

  • 我们进行了调整后的间接比较,纳入了托法替布、巴瑞替尼、乌帕替尼和菲戈替尼的随机临床试验,以评估它们在此情况下的等效性。

  • 我们的结果表明,与乌帕替尼相比,巴瑞替尼和菲戈替尼是等效的治疗选择。然而,托法替布与乌帕替尼相比,结果存在一些不一致。

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