Park Jun Won, Kim Ju Yeon, Kim Min Jung, Lim Yoo Kyoung, Kim Hyoun-Ah, Kim Jin Hyun, Shin Kichul
Division of Rheumatology, Department of Internal Medicine, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Division of Rheumatology, Department of Internal Medicine, Seoul Metropolitan Government-Seoul Boramae Medical Center, Seoul, Republic of Korea.
Front Med (Lausanne). 2024 Jul 22;11:1418243. doi: 10.3389/fmed.2024.1418243. eCollection 2024.
Tapering biologic agents can be considered for patients with stable disease activity in rheumatoid arthritis (RA). However, the specific strategy for abatacept is uncertain. This study aimed to examine the impact of tapering abatacept on disease activity in RA patients and assess the potential influence of concomitant methotrexate (MTX) treatment.
Using data from the KOBIO registry, we included 505 1 year intervals from 176 patients with RA that initiated abatacept with concomitant MTX at baseline. The intervals were divided into two groups based on the dose quotient (DQ) of abatacept during each period (i.e., the tapering group (DQ < 1) and control group (DQ = 1)). The primary outcome was achieving DAS28-remission at 1 year intervals. Marginal structural models (MSM) were used to minimize confounding caused by an imbalance in time-varying variables.
Abatacept was tapered at 146 (28.9%) intervals, and the mean DQ was 0.68. DAS28-remission was achieved in 207 (41.8%) intervals. Tapering abatacept did not affect the odds of achieving DAS28-remission compared with the control group (OR 1.04 [0.67-1.62]). The odds remained unaffected in the subgroup that continued MTX (OR 1.42 [0.88-2.30]) but not in the subgroup that discontinued MTX (OR 0.26 [0.10-0.57]). The effects of interaction between tapering abatacept and concomitant MTX use on DAS28 and patient's functional status showed consistent results. The incidence of adverse events within a 1 year interval was comparable between the two groups.
Withdrawal of MTX while tapering abatacept may compromise meeting the treatment goal for patients with RA.
对于类风湿关节炎(RA)病情活动稳定的患者,可考虑逐渐减少生物制剂的使用。然而,阿巴西普的具体减量策略尚不确定。本研究旨在探讨阿巴西普减量对RA患者疾病活动度的影响,并评估同时使用甲氨蝶呤(MTX)治疗的潜在影响。
利用KOBIO注册研究的数据,我们纳入了176例在基线时开始使用阿巴西普并联合MTX治疗的RA患者的505个1年时间段。根据每个时间段内阿巴西普的剂量商(DQ)将这些时间段分为两组(即减量组(DQ < 1)和对照组(DQ = 1))。主要结局是每隔1年达到DAS28缓解。使用边际结构模型(MSM)来最小化由时变变量不平衡引起的混杂因素。
在146个(28.9%)时间段内阿巴西普进行了减量,平均DQ为0.68。在207个(41.8%)时间段内实现了DAS28缓解。与对照组相比,逐渐减少阿巴西普的使用并不影响达到DAS28缓解的几率(OR 1.04 [0.67 - 1.62])。在继续使用MTX的亚组中几率保持不受影响(OR 1.42 [0.88 - 2.30]),但在停用MTX的亚组中则不然(OR 0.26 [0.10 - 0.57])。逐渐减少阿巴西普与同时使用MTX对DAS28和患者功能状态的相互作用影响显示出一致的结果。两组在1年时间段内不良事件的发生率相当。
在逐渐减少阿巴西普用量的同时停用MTX可能会影响RA患者实现治疗目标。