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タイトル: Infliximab Treatment Persistence among Japanese Patients with Chronic Inflammatory Diseases: A Retrospective Japanese Claims Data Study
著者: Masui, Sho
Yonezawa, Atsushi  KAKEN_id  orcid https://orcid.org/0000-0002-8057-6768 (unconfirmed)
Momo, Kenji
Nakagawa, Shunsaku  kyouindb  KAKEN_id
Itohara, Kotaro
Imai, Satoshi  KAKEN_id
Nakagawa, Takayuki  KAKEN_id  orcid https://orcid.org/0000-0003-1890-0843 (unconfirmed)
Matsubara, Kazuo
著者名の別形: 増井, 翔
米澤, 淳
中川, 俊作
糸原, 光太郎
今井, 哲司
中川, 貴之
松原, 和夫
キーワード: chronic inflammatory disease
Infliximab
real-world database
therapeutic persistence
treatment pattern
発行日: Mar-2022
出版者: Pharmaceutical Society of Japan
誌名: Biological and Pharmaceutical Bulletin
巻: 45
号: 3
開始ページ: 323
終了ページ: 332
抄録: Infliximab (IFX) has contributed to the treatment of several chronic inflammatory diseases, including Crohn's disease (CD), ulcerative colitis (UC), psoriasis (Pso), and rheumatoid arthritis (RA). However, the loss of response in some patients with long-term IFX therapy has been a major problem. Randomized controlled trials (RCTs) are limited in their short duration and lack of generalizability to the real-world population. We aimed to describe the persistence rates of IFX therapy to estimate its long-term effectiveness in clinical practice. Claims data from the Japan Medical Data Center database from January 2005 to June 2017 were used. The study population was identified based on the International Classification of Diseases, 10th Revision and the Anatomical Therapeutic Chemical Classification System. The 5-year persistence rates of IFX therapy were estimated using the Kaplan-Meier method. Overall, 281, 235, 41, and 222 patients with CD, UC, Pso, and RA, respectively, were selected. The 5-year persistence rates for IFX claims were 62.9, 38.9, 22.1, and 28.1% in patients with CD, UC, Pso, and RA, respectively. Patients with CD and UC administered IFX beyond the median dose had higher persistence rates. In patients with RA, female sex and no prior use of other biologics were associated with longer persistence. In conclusion, IFX persistence rates differed across chronic inflammatory diseases, which did not correspond to the results of the major RCTs. Factors associated with longer IFX persistence were identified in each disease group. Our findings may provide useful information to facilitate the proper use of IFX.
著作権等: © 2022 The Pharmaceutical Society of Japan
URI: http://hdl.handle.net/2433/268973
DOI(出版社版): 10.1248/bpb.b21-00906
PubMed ID: 35228398
出現コレクション:学術雑誌掲載論文等

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