自身免疫性疾病患者实际使用 Janus 激酶抑制剂和生物制剂后患间质性肺病的安全风险:利用日本全国电子病历数据库进行的流行病学研究。

IF 2.7 Q3 IMMUNOLOGY
Immunological Medicine Pub Date : 2024-09-01 Epub Date: 2024-02-21 DOI:10.1080/25785826.2024.2311763
Mihoko Yabuuchi, Kazuhito Yokoyama
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引用次数: 0

摘要

尽管 Janus 激酶抑制剂(JAKi)疗法可用于自身免疫性疾病(AD)患者,但其安全性问题之一--间质性肺病(ILD)--却危及生命。我们利用日本的电子病历数据库开展了一项流行病学回顾性队列研究,评估了 JAKi 的实际使用情况以及 JAKi 治疗的安全性。在 391,565 例 AD 患者中,我们分析了 2013 年 7 月至 2022 年 5 月期间接受 JAKi 或肿瘤坏死因子α抑制剂(TNFi)/生物制剂治疗的新用户数据。ILD(ICD10:J70.2、J70.3、J70.4 和 J84)标准被定义为:新ILD(1)和新ILD(2),其不同之处在于后者在ILD发生时会立即停止治疗。我们分析了957名JAKi和3931名TNFi使用者的ILD发生和死亡情况、Kaplan-Meier法的ILD累积发生率以及Cox模型的危险比(HR)。在新药不断开发的同时,JAKi的使用也越来越广泛。在JAKi使用者中,两年新增ILD (2)发病率为1.4%,高于TNFi使用者(风险比:新增ILD (2) 1.75,死亡 2.31)。累积发病率(20.48天内2.9%)也明显更高(对数秩检验p = .013,HR 2.23(95% CI 1.16-4.27));根据HR估算的风险因素包括JAKi(2.14)、类风湿性关节炎(4.94)、糖尿病(2.67)和脑血管疾病(2.86)。ILD 筛查至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety risks of interstitial lung disease upon real-world usage of Janus kinase inhibitors and biologics for patients with autoimmune diseases: epidemiological study using nationwide electronic medical record database in Japan.

Although Janus kinase inhibitor (JAKi) therapy is used for patients with autoimmune diseases (AD), one safety concern, interstitial lung disease (ILD), is life-threatening. We evaluated actual usage of JAKi and safety upon JAKi treatment, in an epidemiological retrospective cohort study utilizing the electronic medical record database in Japan. Among 391,565 AD patients, we analyzed data of new-users receiving JAKi or tumor necrosis factor alpha inhibitor (TNFi)/biologics during the period July 2013-May 2022. ILD (ICD10: J70.2, J70.3, J70.4 and J84) criteria were defined: new-ILD (1) and new-ILD (2) which differed in the latter's prompter therapeutics cessation upon ILD development. We analyzed ILD occurrence and death, ILD cumulative incidence by the Kaplan-Meier method, and hazard ratio (HR) by the Cox model, for 957 JAKi and 3931 TNFi users. JAKi use has become widespread amidst additional drug-development. Among JAKi users, two-year new-ILD (2) incidence, at 1.4%, was higher than for TNFi users (risk ratio: new-ILD (2) 1.75, death 2.31). Cumulative incidence (2.9% in 20.48 days) was also significantly higher (log-rank test p = .013, HR 2.23 (95% CI 1.16-4.27)); risk factors estimated by HR included JAKi (2.14), rheumatoid arthritis (4.94), diabetes mellitus (2.67) and cerebrovascular disease (2.86). ILD screening is essential.

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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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