共 34 条
Association of first, second, and third-line bDMARDs and tsDMARD with drug survival among seropositive rheumatoid arthritis patients: Cohort study in A real world setting
被引:15
作者:

Choi, Seulggie
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机构:
Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Ghang, Byeongzu
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机构:
Jeju Natl Univ, Sch Med, Jeju Natl Univ Hosp, Dept Internal Med,Div Rheumatol, Jeju, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Jeong, Seogsong
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Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Choi, Daein
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机构:
Icahn Sch Med Mt Sinai, Mt Sinai Beth Israel, Dept Internal Med, New York, NY 10029 USA Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Lee, Jeong Seok
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机构:
Genome Insight Inc, Daejeon, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Park, Sang Min
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机构:
Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
Seoul Natl Univ Hosp, Dept Family Med, Seoul, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea

Lee, Eun Young
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机构:
Seoul Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, 101 Daehak Ro, Seoul, South Korea
Seoul Natl Univ, Grad Sch, Integrated Major Innovat Med Sci, Seoul, South Korea Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
机构:
[1] Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
[2] Jeju Natl Univ, Sch Med, Jeju Natl Univ Hosp, Dept Internal Med,Div Rheumatol, Jeju, South Korea
[3] Icahn Sch Med Mt Sinai, Mt Sinai Beth Israel, Dept Internal Med, New York, NY 10029 USA
[4] Genome Insight Inc, Daejeon, South Korea
[5] Seoul Natl Univ Hosp, Dept Family Med, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, 101 Daehak Ro, Seoul, South Korea
[7] Seoul Natl Univ, Grad Sch, Integrated Major Innovat Med Sci, Seoul, South Korea
关键词:
Biologic disease-modifying anti-rheumatic;
drugs;
Drug survival;
Rheumatoid arthritis;
ANTITUMOR NECROSIS FACTOR;
MODIFYING ANTIRHEUMATIC DRUGS;
BIOLOGIC THERAPY;
METHOTREXATE;
GUIDELINES;
MECHANISM;
OUTCOMES;
KOREA;
D O I:
10.1016/j.semarthrit.2021.06.002
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives: To determine the association of first, second, and third-line biologic disease-modifying antirheumatic drugs (bDMARDs) and tofacitinib with drug survival among seropositive rheumatoid arthritis (RA) patients. Methods: The study population was composed of 8,018 seropositive RA patients who were prescribed bDMARDs or tofacitinib between January 2014 and January 2019 from the Korean Health Insurance Review and Assessment Service database. First, second, and third-line choice of tumor necrosis factor inhibitors (TNFi) including etanercept, infliximab, adalimumab, and golimumab, as well as non-TNFi including tocilizumab, rituximab, tofacitinib, and abatacept were assessed. Multivariate Cox proportional hazards regression was used to determine the adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) for drug failure according to bDMARD or tofacitinib choice starting from the initial prescription date. Results: Compared to first etanercept users, patients with first tocilizumab (aHR 0.56, 95% CI 0.46-0.68), tofacitinib (aHR 0.27, 95% CI 0.18-0.42), or abatacept (aHR 0.83, 95% CI 0.69-0.99) had lower risk of drug failure. Second choice of tocilizumab (aHR 0.38, 95% CI 0.25-0.55), tofacitinib (aHR 0.23, 95% CI 0.15-0.37), or abatacept (aHR 0.54, 95% CI 0.35-0.84) was associated with lower drug failure risk compared to second etanercept users. Finally, third choice of tocilizumab (aHR 0.32, 95% CI 0.16-0.62) or tofacitinib (aHR 0.35, 95% CI 0.19-0.63) was associated with lower drug failure risk compared to third TNFi users. Conclusion: First and second-line tocilizumab, tofacitinib, or abatacept may lead to improved drug survival. Third-line use of tocilizumab or tofacitinib may be beneficiary in reducing drug failure risk among seropositive RA patients. (c) 2021 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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页码:685 / 691
页数:7
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