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dc.contributor.authorEbina, Kosukeen
dc.contributor.authorHashimoto, Motomuen
dc.contributor.authorYamamoto, Wataruen
dc.contributor.authorOhnishi, Akiraen
dc.contributor.authorKabata, Daijiroen
dc.contributor.authorHirano, Toruen
dc.contributor.authorHara, Ryotaen
dc.contributor.authorKatayama, Masakien
dc.contributor.authorYoshida, Shuzoen
dc.contributor.authorNagai, Kojien
dc.contributor.authorSon, Yonsuen
dc.contributor.authorAmuro, Hidekien
dc.contributor.authorAkashi, Kengoen
dc.contributor.authorFujimura, Takanorien
dc.contributor.authorHirao, Makotoen
dc.contributor.authorYamamoto, Keiichien
dc.contributor.authorShintani, Ayumien
dc.contributor.authorKumanogoh, Atsushien
dc.contributor.authorYoshikawa, Hidekien
dc.contributor.alternative橋本, 求ja
dc.date.accessioned2018-05-14T04:23:14Z-
dc.date.available2018-05-14T04:23:14Z-
dc.date.issued2018-03-15-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2433/231091-
dc.description.abstractThe purpose of this study was to evaluate the retention and discontinuation reasons of seven biological disease-modifying antirheumatic drugs (bDMARDs) in a real-world setting of patients with rheumatoid arthritis (RA). 1, 037 treatment courses with bDMARDs from 2009 to 2016 [female, 81.8%; baseline age, 59.6 y; disease duration 7.8 y; rheumatoid factor positivity 81.5%; Disease Activity Score in 28 joints using erythrocyte sedimentation rate (DAS28-ESR), 4.4; concomitant prednisolone 43.5% and methotrexate 68.6%; Bio-naïve, 57.1%; abatacept (ABT), 21.3%; tocilizumab (TCZ), 20.7%; golimumab (GLM), 16.9%; etanercept (ETN), 13.6%; adalimumab (ADA), 11.1%; infliximab (IFX), 8.5%; certolizumab pegol (CZP), 7.9%] were included in this multi-center, retrospective study. Drug retention and discontinuation reasons at 36 months were estimated using the Kaplan-Meier method and adjusted by potent confounders using Cox proportional hazards modeling. As a result, 455 treatment courses (43.9%) were stopped, with 217 (20.9%) stopping due to inefficacy, 113 (10.9%) due to non-toxic reasons, 86 (8.3%) due to toxic adverse events, and 39 (3.8%) due to remission. Drug retention rates in the adjusted model were as follows: total retention (ABT, 60.7%; ADA, 32.7%; CZP, 43.3%; ETN, 51.9%; GLM, 45.4%; IFX, 31.1%; and TCZ, 59.2%; P < 0.001); inefficacy (ABT, 81.4%; ADA, 65.7%; CZP, 60.7%; ETN, 71.3%; GLM, 68.5%; IFX, 65.0%; and TCZ, 81.4%; P = 0.015), toxic adverse events (ABT, 89.8%; ADA, 80.5%; CZP, 83.9%; ETN, 89.2%; GLM, 85.5%; IFX, 75.6%; and TCZ, 77.2%; P = 0.50), and remission (ABT, 95.5%; ADA, 88.1%; CZP, 91.1%; ETN, 97.5%; GLM, 94.7%; IFX, 86.4%; and TCZ, 98.4%; P < 0.001). In the treatment of RA, ABT and TCZ showed higher overall retention, and TCZ showed lower inefficacy compared to IFX, while IFX showed higher discontinuation due to remission compared to ABT, ETN, GLM, and TCZ in adjusted modeling.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Science (PLoS)en
dc.rights© 2018 Ebina et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.titleDrug retention and discontinuation reasons between seven biologics in patients with rheumatoid arthritis -The ANSWER cohort study-en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitlePLOS ONEen
dc.identifier.volume13-
dc.identifier.issue3-
dc.relation.doi10.1371/journal.pone.0194130-
dc.textversionpublisher-
dc.identifier.artnume0194130-
dc.addressDepartment of Orthopaedic Surgery, Osaka Universityen
dc.addressDepartment of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University・Department of Health Information Management, Kurashiki Sweet Hospitalen
dc.addressDepartment of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicineen
dc.addressDepartment of Medical Statistics, Osaka City University Graduate School of Medicineen
dc.addressDepartment of Respiratory Medicine and Clinical Immunology, Osaka Universityen
dc.addressThe Center for Rheumatic Diseases, Department of Orthopaedic Surgery, Nara Medical Universityen
dc.addressDepartment of Rheumatology, Osaka Red Cross Hospitalen
dc.addressDepartment of Internal Medicine (IV), Osaka Medical Collegeen
dc.addressDepartment of Internal Medicine (IV), Osaka Medical Collegeen
dc.addressFirst Department of Internal Medicine, Kansai Medical Universityen
dc.addressFirst Department of Internal Medicine, Kansai Medical Universityen
dc.addressDepartment of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicineen
dc.addressThe Center for Rheumatic Diseases, Nara Medical Universityen
dc.addressDepartment of Orthopaedic Surgery, Osaka University, Graduate School of Medicineen
dc.addressDepartment of Medical Statistics, Osaka City University Graduate School of Medicineen
dc.addressDepartment of Medical Statistics, Osaka City University Graduate School of Medicineen
dc.addressDepartment of Respiratory Medicine and Clinical Immunology, Osaka University, Graduate School of Medicineen
dc.addressDepartment of Orthopaedic Surgery, Osaka University, Graduate School of Medicineen
dc.identifier.pmid29543846-
dcterms.accessRightsopen access-
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