Efficacy and safety of Janus kinase inhibitors in patients with difficult-to-treat rheumatoid arthritis

被引:0
作者
Anno, Shohei [1 ]
Okano, Tadashi [2 ]
Mamoto, Kenji [3 ]
Yamada, Yutaro [3 ]
Mandai, Koji [4 ]
Orita, Kazuki [1 ]
Iida, Takahiro [5 ,6 ]
Tada, Masahiro [7 ]
Inui, Kentaro [3 ,8 ]
Koike, Tatsuya [9 ]
Nakamura, Hiroaki [3 ]
机构
[1] Yodogawa Christians Hosp, Dept Orthopaed Surg, Osaka, Japan
[2] Osaka Metropolitan Univ, Grad Sch Med, Ctr Senile Degenerat Disorders CSDD, 1-4-3 Asahimachi,Abeno ku, Osaka 5458585, Japan
[3] Osaka Metropolitan Univ, Dept Orthopaed Surg, Grad Sch Med, Osaka, Japan
[4] Mikunioka Mandai Orthoped Clin, Sakai, Japan
[5] Koryokai Hosp, Dept Orthopaed Surg, Osaka, Japan
[6] Takahiro Clin, Dept Orthopead Surg, Nishinomiya, Japan
[7] Osaka City Gen Hosp, Dept Orthopead Surg, Osaka, Japan
[8] Osaka Saiseikai Nakatsu Hosp, Dept Orthopaed Surg, Osaka, Japan
[9] Shirahama Hamayu Hosp, Search Inst Bone & Arthrit Dis SINBAD, Wakayama, Japan
关键词
Difficult-to-treat rheumatoid arthritis; Janus kinase inhibitors; drug retention rate; effectiveness; safety; RHEUMATOLOGY/EUROPEAN LEAGUE; CLINICAL-RESPONSE; AMERICAN-COLLEGE; TOFACITINIB; THERAPY; PLACEBO; BARICITINIB; ADALIMUMAB; REMISSION;
D O I
10.1093/mr/roae077
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: This study evaluated the effectiveness of Janus kinase inhibitors (JAKi) in patients with difficult-to-treat rheumatoid arthritis (D2T RA). Methods: This study included 220 patients with RA who were treated with JAKi. Sixty-two patients were na & iuml;ve to biological disease-modifying antirheumatic drugs (bDMARDs)/JAKi (1st group), 57 patients were failure to one bDMARDs/JAKi (2nd group), and 101 patients were failure to >= 2 bDMARDs/JAKi. Of these 101 patients, 25 did not meet the D2T RA criteria (non-D2T RA group) and 76 met the D2T RA criteria (D2T RA group). Results: DAS28-ESR was improved in all groups at 24 weeks (1st: P < .01, 2nd: P < .01, non-D2T RA: P = .01, D2TRA: P = .02), and improvement ratio of DAS28-ESR was not different between DT2RA group and 2nd (P = .73) or non-D2T RA group (P = .68). Glucocorticoid use [odds ratios: 8.67; 95% confidence interval (CI): 1.23-60.90; P = .03] and number of past bDMARD/JAKi uses >= 3 (odds ratios: 10.55; 95% CI: 1.39-80.30; P = .02) were risk factors for DAS28-ESR >= 3.2 at 24 weeks in the D2T RA group. Conclusions: Clinical efficacy of JAKi in D2T RA group did not differ from that in 2nd and non-D2T RA groups. Glucocorticoid use and multiple bDMARD/JAKi failure were poor prognostic factors for D2T RA.
引用
收藏
页码:225 / 233
页数:9
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