Janus kinase inhibitors vs. abatacept about safety and efficacy for patients with rheumatoid arthritis-associated interstitial lung disease: a retrospective nested case-control study.

IF 2.1 Q3 RHEUMATOLOGY
Atsuko Tsujii, Kentaro Isoda, Maiko Yoshimura, Akihiko Nakabayashi, Dong-Seop Kim, Tatsuya Tamada, Kurumi Yamamoto, Shiro Ohshima
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引用次数: 0

Abstract

Background: Interstitial lung disease (ILD) related to rheumatoid arthritis (RA) is among the leading causes of death and an essential prognostic factor. There is only limited evidence for the safety of anti-rheumatic drugs for patients with RA-ILD. The aim of this study is to investigate the safety and efficacy of Janus kinase inhibitors (JAKis) by comparing it with abatacept (ABT) in patients with RA-ILD.

Methods: This single centre, retrospective nested case-control study enrolled patients with RA-ILD treated with JAKi or ABT. To determine the safety of the two drugs for existing ILD, we compared their drug persistency, incidence rates of pulmonary complications, and change of chest computed tomography (CT) image. For their efficacy as RA treatment, disease activity scores and prednisolone (PSL)-sparing effect were compared. We performed propensity score matching to match the groups' patient characteristics.

Results: We studied 71 patients with RA-ILD (ABT, n = 45; JAKi, n = 26). At baseline, the JAKi group had longer disease duration, longer duration of past bDMARD or JAKi use and higher usual interstitial pneumonia rate. After propensity score matching, no significant differences in patient characteristics were found between the two groups. No significant difference in the drug persistency rate for the first 2 years (ABT, 61.9%; JAKi, 42.8%; P = 0.256) was observed between the two matched groups. The incidence rate of pulmonary complications did not differ significantly between the two groups (P = 0.683). The CT score did not change after the treatment for the ABT group (Ground-glass opacities (GGO): P = 0.87; fibrosis: P = 0.78), while the GGO score significantly improved for the JAKi group (P = 0.03), although the number was limited (ABT: n = 7; JAKi: n = 8). The fibrosis score of the JAKi group did not change significantly.(P = 0.82). Regarding the efficacy for RA, a significant decrease in disease activity scores after the 1-year treatment was observed in both groups, and PSL dose was successfully tapered, although no significant differences were observed between the two drugs.

Conclusions: JAKi is as safe and effective as ABT for patients with RA-ILD. JAKi can be a good treatment option for such patients.

类风湿性关节炎相关间质性肺病患者使用 Janus 激酶抑制剂与阿巴他赛普的安全性和有效性对比:一项回顾性巢式病例对照研究。
背景:与类风湿性关节炎(RA)相关的间质性肺病(ILD)是导致死亡的主要原因之一,也是一个重要的预后因素。关于抗风湿药物对 RA-ILD 患者的安全性,目前只有有限的证据。本研究旨在通过比较 Janus 激酶抑制剂(JAKis)与阿巴他赛(ABT)对 RA-ILD 患者的安全性和有效性:这项单中心回顾性巢式病例对照研究招募了接受JAKi或ABT治疗的RA-ILD患者。为了确定这两种药物对现有 ILD 的安全性,我们比较了它们的药物持续性、肺部并发症的发生率以及胸部计算机断层扫描(CT)图像的变化。至于它们作为 RA 治疗药物的疗效,我们比较了疾病活动度评分和泼尼松龙(PSL)的节省效果。我们进行了倾向得分匹配,以匹配各组患者的特征:我们研究了71名RA-ILD患者(ABT,n = 45;JAKi,n = 26)。基线时,JAKi组的病程更长,既往使用bDMARD或JAKi的时间更长,通常间质性肺炎的发病率更高。经过倾向评分匹配后,两组患者的特征无明显差异。两组患者在头两年的持续用药率(ABT,61.9%;JAKi,42.8%;P = 0.256)无明显差异。肺部并发症的发生率在两组间无明显差异(P = 0.683)。ABT 组的 CT 评分在治疗后没有变化(地玻璃不透明(GGO),P = 0.87;纤维化,P = 0.87):P = 0.87;纤维化:P=0.78),而JAKi组的GGO评分明显改善(P=0.03),但数量有限(ABT:n=7;JAKi:n=8)。JAKi组的纤维化评分没有明显变化(P = 0.82)。在对RA的疗效方面,治疗1年后,两组的疾病活动评分均显著下降,PSL剂量也成功减量,但两种药物之间未观察到显著差异:结论:对于RA-ILD患者来说,JAKi与ABT一样安全有效。结论:对于RA-ILD患者,JAKi与ABT一样安全有效,JAKi可以成为此类患者的良好治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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