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https://doi.org/10.24546/81003963
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2026-08-11
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81003963 (fulltext)
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81003963
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open access
出版タイプ
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タイトル
A Study on the Selection of DMARDs for the Combination Therapy with Adalimumab
著者
Tanaka, Chihiro ; Shiozawa, Kazuko ; Hashiramoto, Akira ; Shiozawa, Shunichi
著者名
Tanaka, Chihiro
著者名
Shiozawa, Kazuko
著者名
Hashiramoto, Akira
著者名
Shiozawa, Shunichi
言語
English (英語)
収録物名
The Kobe journal of the medical sciences
巻(号)
58(2)
ページ
41-50
出版者
神戸大学医学部
Kobe University School of Medicine
刊行日
2012
公開日
2012-07-09
抄録
We evaluated whether or not the effect of adalimumab (ADA) in combination with the disease-modifying antirheumatic drugs (DMARDs) other than methotrexate (MTX) is comparable to the ADA+MTX therapy for the treatment of rheumatoid arthritis (RA). A total of 216 patients with active RA at Kohnan Kakogawa Hospital and Kobe University Hospital were enrolled. Clinical and functional outcomes were compared among 4 groups, ADA alone (A group), ADA + MTX (B group), ADA + MTX + other DMARDs (C group), and ADA + other DMARDs (D group), and the retention rates of ADA were evaluated with or without MTX. CRP was significantly decreased from initial measurement at 1 month in all 4 groups, but the continuous efficacy with the statistical significance at all measurement points were observed only in combination with MTX (P<0.05), which was reflected by significantly higher retention rates. Similarly, the disease activities were improved, and particularly the remission rates (DAS28-CRP < 2.3) of A, B and C groups (>42.9%) were higher than that of D group (29.4%) at 2 year. An index of patients’ basic activities of daily living, M-HAQ score of A, B and C groups was also better than that of D group. While, looking at the mean changes of M-HAQ from the baseline at 2 years, potential effect of other DMARDs on M-HAQ was also suggested. The results show that ADA + MTX therapy is significantly superior than ADA + other DMARDs in ameliorating RA.
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The Kobe journal of the medical sciences
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58巻
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58巻2号(2012)
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http://www.med.kobe-u.ac.jp/journal/contents.html
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departmental bulletin paper
ISSN
0023-2513
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AA00711740
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