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Kobayashi, Taku Center for Advanced IBD Research and Treatment, Kitasato University Kitasato Institute Hospital
Hisamatsu, Tadakazu Department of Gastroenterology and Hepatology, Kyorin University School of Medicine
Motoya, Satoshi Inflammatory Bowel Disease Center, Sapporo-Kosei General Hospital
Fujii, Toshimitsu Department of Gastroenterology and Hepatology, Institute of Science Tokyo
Kunisaki, Reiko Inflammatory Bowel Disease Center, Yokohama City University Medical Center
Shibuya, Tomoyoshi Department of Gastroenterology, Juntendo University School of Medicine
Matsuura, Minoru Department of Gastroenterology and Hepatology, Kyorin University School of Medicine
Takeuchi, Ken Department of Gastroenterology and Hepatology, IBD Center
Hiraoka, Sakiko Department of Gastroenterology and Hepatology, Okayama University Hospital Kaken ID publons researchmap
Yasuda, Hiroshi Department of Gastroenterology, St. Marianna University School of Medicine
Yokoyama, Kaoru Department of Gastroenterology, Kitasato University School of Medicine
Takatsu, Noritaka Inflammatory Bowel Disease Center, Fukuoka University Chikushi Hospital
Maemoto, Atsuo Inflammatory Bowel Disease Center, Sapporo Higashi Tokushukai Hospital
Tahara, Toshiyuki Department of Gastroenterology, Saiseikai Utsunomiya Hospital
Tominaga, Keiichi Department of Gastroenterology, Dokkyo Medical University
Shimada, Masaaki Department of Gastroenterology, NHO Nagoya Medical Center
Kuno, Nobuaki Department of Gastroenterology and Medicine, Fukuoka University Hospital
Fernandez, Jovelle L. Japan Medical Office, Takeda Pharmaceutical Company Limited
Ishiguro, Kaori Japan Medical Office, Takeda Pharmaceutical Company Limited
Cavaliere, Mary Japan Medical Office, Takeda Pharmaceutical Company Limited
Deguchi, Hisato Japan Medical Office, Takeda Pharmaceutical Company Limited
Hibi, Toshifumi Center for Advanced IBD Research and Treatment, Kitasato University Kitasato Institute Hospital
Abstract
Background/Aims The objectives of this real-world study were to determine 1-year persistence with vedolizumab in patients with ulcerative colitis and to evaluate factors contributing to loss of response.
Methods In this multicenter, retrospective, observational chart review, patients with moderately to severely active ulcerative colitis who received ≥ 1 dose of vedolizumab in clinical practice at 16 tertiary hospitals in Japan (from December 2018 through February 2020) were enrolled.
Results Persistence with vedolizumab was 64.5% (n = 370); the median follow-up time was 53.2 weeks. Discontinuation due to loss of response among initial clinical remitters was reported in 12.5% (35/281) of patients. Multivariate analysis showed that concomitant use of tacrolimus (odds ratio [OR], 2.76; 95% confidence interval [CI], 1.00–7.62; P= 0.050) and shorter disease duration (OR for median duration ≥ 7.8 years vs. < 7.8 years, 0.33; 95% CI, 0.13–0.82; P= 0.017) were associated with discontinuation due to loss of response. Loss of response was not associated with prior use of anti-tumor necrosis factor alpha therapy, age at the time of treatment, disease severity, or concomitant corticosteroids or immunomodulators. Of the 25 patients with disease duration < 1 year, 32.0% discontinued due to loss of response.
Conclusions Persistence with vedolizumab was consistent with previous reports. Use of tacrolimus and shorter disease duration were the main predictors of decreased persistence.
Keywords
Colitis, ulcerative
Inflammatory bowel diseases
Japan
Vedolizumab
Medication persistence
Published Date
2025-01-16
Publication Title
Intestinal Research
Publisher
Korean Association for the Study of Intestinal Diseases
ISSN
1598-9100
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2025 Korean Association for the Study of Intestinal Diseases.
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publisher
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DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.5217/ir.2024.00063
License
http://creativecommons.org/licenses/by-nc/4.0/
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( 武田薬品工業株式会社 / Takeda Pharmaceutical Company Limited )