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依那西普治疗甲氨蝶呤耐药的类风湿关节炎的有效阈剂量。

The effective threshold dose of etanercept in patients with methotrexate-resistant rheumatoid arthritis.

机构信息

Department of Rheumatology, Ren Ji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.

Department of Pharmacy, Huangpu Branch, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

Clin Rheumatol. 2023 Oct;42(10):2777-2786. doi: 10.1007/s10067-023-06659-9. Epub 2023 Jul 7.

Abstract

INTRODUCTION

The therapy of rheumatoid arthritis (RA) was advanced by biological agents, yet costly. This study aims to identify the effective threshold dose of etanercept (ENT) and cost-effectiveness in methotrexate (MTX)-resistant RA in real world.

METHODS

Eligible patients had an inadequate response (DAS28-ESR > 3.2) to initial MTX monotherapy, and subsequently received etanercept. The effective cut-off value of cumulative dose was identified to maintain remission response (DAS28-ESR < 2.6) at month 24 by using restricted cubic splines. Remission rate, low disease activity (LDA) rate, glucocorticoid exposure, safety, and cost-effectiveness were compared between the saturated and non-saturated dose groups divided by the cut-off dose.

RESULTS

Seventy-eight (14.2%) of 549 enrolled patients were eligible, and 72 patients completed follow-up. The 2-year cumulative cut-off dose that maintained remission response at 24 months was 1975 mg. And the recommended threshold dosing strategy of etanercept was twice weekly (BIW) for the first 6 months, every week (QW) for the next 6 months, and every 2 weeks (Q2W) and every month (QM) for the second year. Greater net changes in DAS28-ESR score were observed in the ENT saturated dose group than in the non-saturated dose group (average change 0.569, 95%CI 0.236-0.901, p = 0.001). The proportion of patients achieving remission (27.8% vs 72.2%, p < 0.001) and LDA (58.3% vs 83.3%, p = 0.020) in the non-saturated group was both significantly lower than that in the saturated group at 24 months. The incremental cost-effectiveness ratio of the saturated group referred to the non-saturated group was 5791.2 $/QALY.

CONCLUSIONS

In refractory RA patients, the effective cumulative cut-off dose of etanercept for sustained remission at 24 months was calculated as 1975 mg, and receiving saturated dose was more effective and cost-effective than with non-saturated dose. Key Points • The effective cumulative cut-off dose of etanercept for sustained remission at 24 months in RA patients is calculated as 1975 mg. • Receiving saturated dose of etanercept is more effective and cost-effective than with non-saturated dose in refractory RA patients.

摘要

简介

类风湿关节炎(RA)的治疗取得了生物制剂的进展,但费用昂贵。本研究旨在确定依那西普(ENT)在真实世界中对甲氨蝶呤(MTX)耐药性 RA 的有效阈值剂量和成本效益。

方法

符合条件的患者对初始 MTX 单药治疗反应不足(DAS28-ESR>3.2),随后接受依那西普治疗。通过受限立方样条,确定累积剂量的有效截止值,以在第 24 个月保持缓解反应(DAS28-ESR<2.6)。通过截止剂量将患者分为饱和剂量组和非饱和剂量组,比较两组的缓解率、低疾病活动率(LDA)、糖皮质激素暴露、安全性和成本效益。

结果

549 名入组患者中,有 78 名(14.2%)符合条件,72 名患者完成了随访。在第 24 个月时保持缓解反应的 2 年累积截止剂量为 1975mg。依那西普的推荐阈值给药方案为前 6 个月每周两次(BIW),接下来 6 个月每周一次(QW),第二年每 2 周(Q2W)和每月一次(QM)。在 ENT 饱和剂量组中,DAS28-ESR 评分的净变化大于非饱和剂量组(平均变化 0.569,95%CI 0.236-0.901,p=0.001)。在第 24 个月时,非饱和组达到缓解(27.8% vs 72.2%,p<0.001)和 LDA(58.3% vs 83.3%,p=0.020)的患者比例均显著低于饱和组。饱和组的增量成本效益比相对于非饱和组为 5791.2 美元/QALY。

结论

在难治性 RA 患者中,依那西普持续缓解 24 个月的有效累积截止剂量计算为 1975mg,接受饱和剂量比非饱和剂量更有效且更具成本效益。

关键点

  • 在 RA 患者中,依那西普持续缓解 24 个月的有效累积截止剂量计算为 1975mg。

  • 与非饱和剂量相比,在难治性 RA 患者中接受依那西普饱和剂量更有效且更具成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f43/10497429/9210532859c8/10067_2023_6659_Fig1_HTML.jpg

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