Department of Rheumatology, Japanese Red Cross Fukushima Hospital, Yashima, Fukushima, Japan.
Department of Rheumatology, Fukushima Medical University School of Medicine, Hikarigaoka, Fukushima, Fukushima, Japan.
Medicine (Baltimore). 2022 Oct 21;101(42):e31161. doi: 10.1097/MD.0000000000031161.
In this retrospective cohort study, we compared the retention rates and effectiveness of biologic disease modifying antirheumatic drugs (bDMARDs) and targeted synthetic DMARDs (targeted disease modifying antirheumatic drug [tsDMARDs]: Janus kinase inhibitors [JAKi]) in elderly patients with RA. One hundred thirty-four elderly RA patients (≥65 years) who were initiated with bDMARDs (n = 80) or JAKi (n = 54) between 2016 and 2020 in our institute were enrolled in this analysis. Follow-up was conducted at 4-week intervals from the start of bDMARDs or JAKi. We compared the drug retention and clinical response at 24 week between elderly RA patients treated with bDMARDs and JAKi. In the demographic data, more disease duration, the proportion of previous bDMARDs use and less the proportion of glucocorticoid use in JAKi group was significantly observed compared to the bDMARDs group. Otherwise, there was no significant difference in the other variables between the bDMARDs and JAKi groups. In the JAKi group, drug retention rate was not significantly different compared to the bDMARDs group (HR: 0.723, 95% CI: 0.406-1.289, P = .266). Also, there was no significant difference in the proportion of patients achieving good or moderate European alliance of associations for rheumatology (EULAR) response at 24 week between these two groups (bDMARDs; 88.6% vs JAKi; 91.8%, P = .158). In elderly RA patients initiated with bDMARDs or JAKi, drug retention rates of these targeted therapies did not differ significantly between these two groups. These findings suggest that elderly RA patients can achieve similar clinical improvement after initiating bDMARDs or JAKi.
在这项回顾性队列研究中,我们比较了生物改良抗风湿药物(bDMARDs)和靶向合成 DMARDs(靶向疾病改良抗风湿药物[tsDMARDs]:Janus 激酶抑制剂[JAKi])在老年类风湿关节炎(RA)患者中的保留率和疗效。我们纳入了 134 名在 2016 年至 2020 年期间在我院接受 bDMARDs(n=80)或 JAKi(n=54)治疗的老年 RA 患者,对他们进行了这项分析。从 bDMARDs 或 JAKi 开始治疗后,每 4 周进行一次随访。我们比较了老年 RA 患者接受 bDMARDs 和 JAKi 治疗 24 周时的药物保留率和临床反应。在人口统计学数据中,与 bDMARDs 组相比,JAKi 组患者的疾病持续时间更长、以前使用过 bDMARDs 的比例更高、使用糖皮质激素的比例更低。其他变量在 bDMARDs 和 JAKi 两组之间没有显著差异。在 JAKi 组,与 bDMARDs 组相比,药物保留率没有显著差异(HR:0.723,95%CI:0.406-1.289,P=0.266)。此外,两组患者在 24 周时达到良好或中度欧洲抗风湿病联盟(EULAR)反应的比例也没有显著差异(bDMARDs:88.6%vs JAKi:91.8%,P=0.158)。在开始接受 bDMARDs 或 JAKi 治疗的老年 RA 患者中,这两种靶向治疗的药物保留率在两组之间没有显著差异。这些发现表明,老年 RA 患者在开始接受 bDMARDs 或 JAKi 治疗后可以获得相似的临床改善。