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dc.contributor.authorMasui, Shoen
dc.contributor.authorYonezawa, Atsushien
dc.contributor.authorMomo, Kenjien
dc.contributor.authorNakagawa, Shunsakuen
dc.contributor.authorItohara, Kotaroen
dc.contributor.authorImai, Satoshien
dc.contributor.authorNakagawa, Takayukien
dc.contributor.authorMatsubara, Kazuoen
dc.contributor.alternative増井, 翔ja
dc.contributor.alternative米澤, 淳ja
dc.contributor.alternative中川, 俊作ja
dc.contributor.alternative糸原, 光太郎ja
dc.contributor.alternative今井, 哲司ja
dc.contributor.alternative中川, 貴之ja
dc.contributor.alternative松原, 和夫ja
dc.date.accessioned2022-03-24T02:17:20Z-
dc.date.available2022-03-24T02:17:20Z-
dc.date.issued2022-03-
dc.identifier.urihttp://hdl.handle.net/2433/268973-
dc.description.abstractInfliximab (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.en
dc.language.isoeng-
dc.publisherPharmaceutical Society of Japanen
dc.publisher.alternative日本薬学会ja
dc.rights© 2022 The Pharmaceutical Society of Japanen
dc.subjectchronic inflammatory diseaseen
dc.subjectInfliximaben
dc.subjectreal-world databaseen
dc.subjecttherapeutic persistenceen
dc.subjecttreatment patternen
dc.titleInfliximab Treatment Persistence among Japanese Patients with Chronic Inflammatory Diseases: A Retrospective Japanese Claims Data Studyen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleBiological and Pharmaceutical Bulletinen
dc.identifier.volume45-
dc.identifier.issue3-
dc.identifier.spage323-
dc.identifier.epage332-
dc.relation.doi10.1248/bpb.b21-00906-
dc.textversionpublisher-
dc.identifier.pmid35228398-
dcterms.accessRightsopen access-
datacite.awardNumber19H03389-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H03389/-
dc.identifier.pissn0918-6158-
dc.identifier.eissn1347-5215-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle抗体医薬品に対する抗薬物抗体の実態解明と臨床疫学解析ja
出現コレクション:学術雑誌掲載論文等

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