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巴瑞替尼治疗西班牙类风湿关节炎的真实世界证据:一项系统文献综述

Real-World Evidence for Baricitinib in the Treatment of Rheumatoid Arthritis in Spain: A Systematic Literature Review.

作者信息

Rosas José, Belzunegui Joaquín, Hernández-Cruz Blanca, Aguirregabiria Itxaso, Moyano Sebastián, Cobo Amelia, Díaz-Cerezo Silvia

机构信息

Rheumatology Department, Marina Baixa Hospital, Av. Alcalde En Jaume Botella Mayor, 7, Villajoyosa, 03570, Alicante, Spain.

Rheumatology Department, Donostia University Hospital, Begiristain Doktorea Pasealekua, 20014, Guipúzcoa, Spain.

出版信息

Adv Ther. 2025 May;42(5):2403-2428. doi: 10.1007/s12325-025-03161-3. Epub 2025 Mar 22.

Abstract

INTRODUCTION

Baricitinib is a Janus kinase inhibitor approved for the treatment of moderate-to-severe rheumatoid arthritis (RA) in adults who have responded inadequately, or are intolerant, to disease-modifying antirheumatic drugs (DMARDs). This systematic literature review was conducted to understand the use of baricitinib in RA in the real-world setting in Spain.

METHODS

Embase and MEDLINE databases were systematically searched for publications (in English or Spanish) published between March 2017 and June 2023; Spanish data presented at national rheumatology congresses were also obtained, with a date limitation of 2021-2023.

RESULTS

Nineteen eligible publications were identified (5 full papers, 14 conference abstracts), including more than 1000 patients who received baricitinib for RA in Spain. Most patients were older and female with long disease duration, and moderate-to-severe active disease. Studies included both biologic DMARD-experienced and DMARD-naïve patients, and most patients received baricitinib 4 mg/day. Baricitinib persistence ranged from 6 to 48 months, with ineffectiveness (primary or secondary) being the most frequently reported reason for discontinuation. Baricitinib was consistently shown to decrease disease activity, across all outcome measures (Disease Activity Score-28 for RA, the Simplified and Clinical Disease Activity Indexes, swollen and tender joint counts and patient-reported outcomes). Thirteen studies reported safety outcomes, with discontinuation rates due to adverse events ranging from 9.5 to 20%. Across these studies, adverse events of interest included eleven cases of herpes zoster, six serious infections, two major adverse cardiovascular events, and three malignant neoplasms.

CONCLUSION

These results suggest baricitinib is effective in the real-world setting in Spain, with a consistent safety profile, similar to findings reported in clinical studies and in real-world studies conducted in other countries.

摘要

引言

巴瑞替尼是一种获批用于治疗对改善病情抗风湿药(DMARDs)反应不足或不耐受的成年中重度类风湿关节炎(RA)患者的 Janus 激酶抑制剂。本系统文献综述旨在了解巴瑞替尼在西班牙真实世界中 RA 治疗中的应用情况。

方法

系统检索 Embase 和 MEDLINE 数据库中 2017 年 3 月至 2023 年 6 月发表的(英文或西班牙文)文献;还获取了 2021 - 2023 年在西班牙全国风湿病学大会上展示的西班牙数据。

结果

共识别出 19 篇符合条件的文献(5 篇全文,14 篇会议摘要),包括西班牙 1000 多名接受巴瑞替尼治疗 RA 的患者。大多数患者年龄较大,为女性,病程较长,患有中重度活动性疾病。研究纳入了有生物 DMARD 使用经验和未使用过 DMARD 的患者,大多数患者接受 4mg/天的巴瑞替尼治疗。巴瑞替尼的持续用药时间为 6 至 48 个月,无效(原发性或继发性)是最常报告的停药原因。在所有结局指标(RA 的 28 关节疾病活动评分、简化和临床疾病活动指数、肿胀和压痛关节计数以及患者报告结局)中,巴瑞替尼均持续显示出可降低疾病活动度。13 项研究报告了安全性结局,因不良事件导致的停药率在 9.5%至 20%之间。在这些研究中,关注的不良事件包括 11 例带状疱疹、6 例严重感染、2 例主要不良心血管事件和 3 例恶性肿瘤。

结论

这些结果表明,巴瑞替尼在西班牙的真实世界环境中有效,安全性特征一致,与临床研究及其他国家的真实世界研究报告结果相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da6/12006230/d84bef2bb027/12325_2025_3161_Fig1_HTML.jpg

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