Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Korean J Intern Med. 2024 Sep;39(5):833-844. doi: 10.3904/kjim.2023.297. Epub 2024 May 27.
BACKGROUND/AIMS: The aim of this study was to compare the short- and long-term retention rates of biologic and targeted synthetic disease-modifying anti-rheumatic drugs (b/tsDMARDs) in Korean patients with seropositive rheumatoid arthritis.
This study was conducted with 1,538 treatment courses of 1,063 patients, including adalimumab (n = 332), etanercept (n = 369), infliximab (n = 146), abatacept (n = 152), tocilizumab (n = 299), tofacitinib (n = 136), and baricitinib (n = 104), in patients with seropositive rheumatoid arthritis who started b/tsDMARD treatment between 2008 and 2020 at Seoul St. Mary's Hospital. Discontinuation 1 and 3 years after the first prescription of each drug was investigated. Kaplan- Meier estimates of time to discontinuation were calculated to compare the difference in drug retention rate for each drug. Patient-level predictors of drug discontinuation were evaluated using a Cox proportional hazards model.
The overall 1-year drug retention rate was from 60.1% for adalimumab to 90.0% for tofacitinib in the b/tsDMARD-naïve group, and from 55.2% for infliximab to 84.8% for tofacitinib in the b/tsDMARD-experienced group. The 3-year drug retention rate was from 36.9% for infliximab to 86.5% for tofacitinib in the b/tsDMARD-naïve group, and from 31.0% for infliximab to 65.4% for tocilizumab in the b/tsDMARD-experienced group. Drug discontinuation appeared to be affected by specific types of b/tsDMARDs.
Tocilizumab and tofacitinib are less commonly discontinued compared to tumor necrosis factor-α inhibitors at 1 and 3 years. Specifically, tofacitinib in the b/tsDMARD-naïve group and tocilizumab in the b/tsDMARD-experienced group showed the highest 3-year retention rates.
背景/目的:本研究旨在比较生物制剂和靶向合成的疾病修正抗风湿药物(b/tsDMARDs)在韩国血清阳性类风湿关节炎患者中的短期和长期保留率。
这项研究共纳入了 1063 名患者的 1538 个治疗疗程,其中包括阿达木单抗(n = 332)、依那西普(n = 369)、英夫利昔单抗(n = 146)、阿巴西普(n = 152)、托珠单抗(n = 299)、托法替布(n = 136)和巴瑞替尼(n = 104),这些患者在 2008 年至 2020 年期间于首尔圣玛丽医院开始接受 b/tsDMARD 治疗。研究调查了每种药物首次处方后 1 年和 3 年的停药情况。使用 Kaplan-Meier 估计计算药物停药时间,以比较每种药物的药物保留率差异。使用 Cox 比例风险模型评估药物停药的患者水平预测因素。
在 b/tsDMARD 初治组中,阿达木单抗的总体 1 年药物保留率为 60.1%,托法替布为 90.0%,在 b/tsDMARD 经验组中,英夫利昔单抗为 55.2%,托法替布为 84.8%。在 b/tsDMARD 初治组中,英夫利昔单抗的 3 年药物保留率为 36.9%,托法替布为 86.5%,在 b/tsDMARD 经验组中,英夫利昔单抗为 31.0%,托珠单抗为 65.4%。药物停药似乎受到特定类型的 b/tsDMARDs 的影响。
与肿瘤坏死因子-α抑制剂相比,托珠单抗和托法替布在 1 年和 3 年内的停药率较低。具体而言,在 b/tsDMARD 初治组中,托法替布和在 b/tsDMARD 经验组中,托珠单抗显示出最高的 3 年保留率。