类风湿性关节炎间质性肺病患者皮下注射阿巴他赛普与静脉注射阿巴他赛普的比较。对 397 名患者进行的全国多中心研究

IF 4.6 2区 医学 Q1 RHEUMATOLOGY Seminars in arthritis and rheumatism Pub Date : 2024-07-18 DOI:10.1016/j.semarthrit.2024.152517
Marta López-Maraver , Ana Serrano-Combarro , Belén Atienza-Mateo , Natividad del Val , Ivette Casafont-Solé , Rafael B. Melero-Gonzalez , Alba Pérez-Linaza , Jerusalem Calvo Gutiérrez , Natalia Mena-Vázquez , Nuria Vegas-Revenga , Lucía Domínguez-Casas , Jesús Loarce Martos , Cilia Amparo Peralta Ginés , Carolina Diez Morrondo , Lorena Pérez Albaladejo , Rubén López Sánchez , Mª Guadalupe Manzano Canabal , Anahy Mª Brandy-García , Patricia López Viejo , Gema Bonilla , Ricardo Blanco
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引用次数: 0

摘要

阿巴他赛(ABA)用于治疗类风湿性关节炎(RA)相关间质性肺病(ILD)的证据越来越多。临床试验显示,皮下注射(SC)和静脉注射(IV)阿巴他赛普治疗关节表现的效果相当。然而,尚未对呼吸系统的疗效进行研究。根据给药途径,比较 ABA 对 RA-ILD 患者的疗效。对接受 ABA 治疗的 RA-ILD 患者进行全国性多中心回顾性研究。他们被分为两组:静脉注射组和皮下注射组。采用线性混合模型分析了从基线到最终随访期间的以下结果:肺活量(FVC)、一氧化碳肺弥散能力(DLCO)、胸部高分辨率计算机断层扫描(HRCT)、呼吸困难、RA活动和皮质类固醇疏松效果。共纳入 397 例患者(94 例 IV-ABA 和 303 例 SC-ABA),中位随访时间为 24 [10-48] 个月。在对可能的混杂因素进行调整后,FVC 和 DLCO 在最初的 24 个月中保持稳定,IV-ABA 和 SC-ABA 之间没有差异(= 0.6304 和 0.5337)。67%的患者(75% IV-ABA,64% SC-ABA;= 0.07)在 HRCT 中观察到肺部病变的改善/稳定。84%的患者呼吸困难得到稳定/改善(90% IV-ABA,82% SC-ABA;= 0.09)。RA - 两组患者的疾病活动均有所改善。两组之间的任何研究变量均未发现有统计学意义的差异。87名患者(21.9%)停用了ABA,其中45%为IV-ABA,37%为SC-ABA ( = 0.29)。ILD 恶化和关节无效是停用 ABA 的最常见原因。在RA-ILD患者中,无论采用哪种给药途径,ABA似乎都同样有效。
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Subcutaneous vs intravenous abatacept in rheumatoid arthritis-interstitial lung disease. National multicentre study of 397 patients

Background

Evidence on abatacept (ABA) utility for rheumatoid arthritis (RA) – associated interstitial lung disease (ILD) is growing. Clinical trials have shown equivalence in subcutaneous (SC) and intravenous (IV) administration of ABA for articular manifestations. However, this has not been studied in respiratory outcomes.

Objective

To compare the effectiveness of ABA in RA-ILD patients according to the route of administration.

Methods

National retrospective multicentre study of RA-ILD patients on treatment with ABA. They were divided into 2 groups: a) IV, and b) SC. The following outcomes were analysed from baseline to final follow-up using linear mixed models: a) forced vital capacity (FVC), b) diffusing capacity of the lungs for carbon monoxide (DLCO), c) chest high resolution computed tomography (HRCT), d) dyspnoea, e) RA activity, and f) sparing corticosteroids effect.

Results

A total of 397 patients were included (94 IV-ABA and 303 SC-ABA), median follow-up of 24 [10–48] months. After adjustment for possible confounders, FVC and DLCO remained stable during the first 24 months without differences between IV-ABA and SC-ABA (p = 0.6304 and 0.5337). Improvement/ stability of lung lesions in HRCT was observed in 67 % of patients (75 % IV-ABA, 64 % SC-ABA; p = 0.07). Dyspnoea stabilized/ improved in 84 % of patients (90 % IV-ABA, 82 % SC-ABA; p = 0.09). RA - disease activity improved in both groups. No statistically significant differences regarding any of the variables studied between the two groups were found. ABA was withdrawn in 87 patients (21.9 %), 45 % IV-ABA and 37 % SC-ABA (p = 0.29). ILD worsening and articular inefficacy were the most common reasons for ABA discontinuation.

Conclusion

In patients with RA-ILD, ABA seems to be equally effective regardless of the route of administration.

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来源期刊
CiteScore
9.20
自引率
4.00%
发文量
176
审稿时长
46 days
期刊介绍: Seminars in Arthritis and Rheumatism provides access to the highest-quality clinical, therapeutic and translational research about arthritis, rheumatology and musculoskeletal disorders that affect the joints and connective tissue. Each bimonthly issue includes articles giving you the latest diagnostic criteria, consensus statements, systematic reviews and meta-analyses as well as clinical and translational research studies. Read this journal for the latest groundbreaking research and to gain insights from scientists and clinicians on the management and treatment of musculoskeletal and autoimmune rheumatologic diseases. The journal is of interest to rheumatologists, orthopedic surgeons, internal medicine physicians, immunologists and specialists in bone and mineral metabolism.
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