Impact of concomitant methotrexate on disease activity in patients with rheumatoid arthritis tapering abatacept: results from KOBIO registry

被引:0
作者
Park, Jun Won [1 ]
Kim, Ju Yeon [1 ]
Kim, Min Jung [2 ]
Lim, Yoo Kyoung [3 ]
Kim, Hyoun-Ah [4 ]
Kim, Jin Hyun [5 ]
Shin, Kichul [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul, South Korea
[2] Seoul Metropolitan Govt Seoul Boramae Med Ctr, Dept Internal Med, Div Rheumatol, Seoul, South Korea
[3] Seoul Metropolitan Govt Boramae Med Ctr, Dept Internal Med, Seoul, South Korea
[4] Ajou Univ, Sch Med, Dept Rheumatol, Suwon, South Korea
[5] Chungnam Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, Daejeon, South Korea
关键词
rheumatoid arthritis; abatacept; methotrexate; tapering; disease activity; ETANERCEPT; THERAPY; REMISSION; MODELS;
D O I
10.3389/fmed.2024.1418243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives 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. Methods 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. Results 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. Conclusion Withdrawal of MTX while tapering abatacept may compromise meeting the treatment goal for patients with RA.
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