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从英夫利昔单抗转换为依那西普治疗类风湿关节炎患者的安全性和有效性:来自一项大型日本上市后监测研究的结果。

Safety and effectiveness of switching from infliximab to etanercept in patients with rheumatoid arthritis: results from a large Japanese postmarketing surveillance study.

机构信息

Hokkaido University Graduate School of Medicine, Hokkaido, Japan.

出版信息

Rheumatol Int. 2012 Jun;32(6):1617-24. doi: 10.1007/s00296-011-1807-0. Epub 2011 Feb 18.

DOI:10.1007/s00296-011-1807-0
PMID:21331576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3364424/
Abstract

Finding an effective treatment strategy for rheumatoid arthritis (RA) patients who have not benefited from previous tumor necrosis factor-α antagonist treatment is important for minimizing RA disease activity and improving patient outcomes. The aim of this study was to compare the safety and effectiveness of etanercept in patients with and without infliximab (IFX) treatment experience. Patients (n = 7,099) from a large postmarketing observational study of etanercept use in Japan were divided into 2 cohorts based on previous IFX use (pre-IFX and non-IFX). Baseline characteristics were assessed in each cohort. Adverse events (AEs) and European League Against Rheumatism (EULAR) responses were monitored every 4 weeks for 24 weeks. At baseline, pre-IFX patients were younger and had fewer comorbidities and a shorter RA duration than non-IFX patients. During the study, pre-IFX patients received concomitant methotrexate more often than non-IFX patients. The incidence of AEs and serious AEs were significantly lower in pre-IFX patients, as was the percentage of patients who discontinued treatment. Both cohorts had significant improvement (P < 0.001) in EULAR responses at the end of the treatment period. This study demonstrated that etanercept was effective and well tolerated in active RA patients with and without prior IFX treatment.

摘要

为了最大程度地降低类风湿关节炎(RA)疾病活动度并改善患者预后,为先前未从肿瘤坏死因子-α拮抗剂治疗中获益的 RA 患者找到有效的治疗策略非常重要。本研究旨在比较依那西普在有和无英夫利昔单抗(IFX)治疗经验患者中的安全性和有效性。根据先前 IFX 使用情况(IFX 前和非 IFX),将来自日本一项大型依那西普使用上市后观察性研究的患者(n=7099)分为 2 个队列。评估了每个队列的基线特征。在 24 周的时间里,每 4 周监测一次不良事件(AE)和欧洲抗风湿病联盟(EULAR)的应答情况。在基线时,IFX 前患者比非 IFX 患者更年轻,合并症更少,RA 病程更短。在研究期间,IFX 前患者比非 IFX 患者更常同时接受甲氨蝶呤治疗。IFX 前患者的 AE 和严重 AE 发生率显著降低,停药患者比例也较低。两个队列在治疗期末均有显著的 EULAR 应答改善(P<0.001)。这项研究表明,依那西普在有和无先前 IFX 治疗的活动期 RA 患者中是有效且耐受良好的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/02f447557dd2/296_2011_1807_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/d7461aad4049/296_2011_1807_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/5fe555e903bb/296_2011_1807_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/02f447557dd2/296_2011_1807_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/d7461aad4049/296_2011_1807_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/5fe555e903bb/296_2011_1807_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b75/3364424/02f447557dd2/296_2011_1807_Fig3_HTML.jpg

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本文引用的文献

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Comparison of methotrexate monotherapy with a combination of methotrexate and etanercept in active, early, moderate to severe rheumatoid arthritis (COMET): a randomised, double-blind, parallel treatment trial.甲氨蝶呤单药疗法与甲氨蝶呤和依那西普联合疗法治疗活动期、早期、中重度类风湿关节炎的比较(COMET):一项随机、双盲、平行治疗试验
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