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A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study
Results from clinical trials show that vedolizumab is an efficacious treatment for inflammatory bowel disease, namely Crohn's disease (CD) and ulcerative colitis (UC). However, there is limited evidence from real-world clinical practice, especially on early clinical experiences in the UK. To de...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831399/ https://www.ncbi.nlm.nih.gov/pubmed/30817598 http://dx.doi.org/10.1097/MD.0000000000014681 |
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author | Cummings, Fraser Gaya, Daniel R. Levison, Scott Subramanian, Sreedhar Owen, Glynn Rathmell, Anna Glen, Fiona Demuth, Dirk Meadowcroft, Simon Irving, Peter M. |
author_facet | Cummings, Fraser Gaya, Daniel R. Levison, Scott Subramanian, Sreedhar Owen, Glynn Rathmell, Anna Glen, Fiona Demuth, Dirk Meadowcroft, Simon Irving, Peter M. |
author_sort | Cummings, Fraser |
collection | PubMed |
description | Results from clinical trials show that vedolizumab is an efficacious treatment for inflammatory bowel disease, namely Crohn's disease (CD) and ulcerative colitis (UC). However, there is limited evidence from real-world clinical practice, especially on early clinical experiences in the UK. To describe real-world early experiences of vedolizumab to treat CD and UC in the UK. A retrospective, chart review study of patients with CD or UC treated with vedolizumab across 5 UK hospitals. All eligible adults (≥18 years at initiation) with a diagnosis of CD and ≥14 weeks of data or UC and ≥10 weeks of data available following vedolizumab initiation were included. Data were analyzed for 112 patients (CD: 66; UC: 46). Patients with CD had a median of 7.4 (interquartile range 5.7–9.4) months follow-up and patients with UC had a median of 7.4 (5.6–10.2) months follow-up post-vedolizumab initiation. Most patients, 80% (53/66) with CD and 89% (41/46) with UC, remained on vedolizumab treatment at the time of data collection. No new safety signals were identified during the study. These results add to the body of evidence supporting vedolizumab as an effective and well-tolerated treatment for CD and UC in real-world clinical practice. |
format | Online Article Text |
id | pubmed-6831399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68313992019-11-19 A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study Cummings, Fraser Gaya, Daniel R. Levison, Scott Subramanian, Sreedhar Owen, Glynn Rathmell, Anna Glen, Fiona Demuth, Dirk Meadowcroft, Simon Irving, Peter M. Medicine (Baltimore) 4500 Results from clinical trials show that vedolizumab is an efficacious treatment for inflammatory bowel disease, namely Crohn's disease (CD) and ulcerative colitis (UC). However, there is limited evidence from real-world clinical practice, especially on early clinical experiences in the UK. To describe real-world early experiences of vedolizumab to treat CD and UC in the UK. A retrospective, chart review study of patients with CD or UC treated with vedolizumab across 5 UK hospitals. All eligible adults (≥18 years at initiation) with a diagnosis of CD and ≥14 weeks of data or UC and ≥10 weeks of data available following vedolizumab initiation were included. Data were analyzed for 112 patients (CD: 66; UC: 46). Patients with CD had a median of 7.4 (interquartile range 5.7–9.4) months follow-up and patients with UC had a median of 7.4 (5.6–10.2) months follow-up post-vedolizumab initiation. Most patients, 80% (53/66) with CD and 89% (41/46) with UC, remained on vedolizumab treatment at the time of data collection. No new safety signals were identified during the study. These results add to the body of evidence supporting vedolizumab as an effective and well-tolerated treatment for CD and UC in real-world clinical practice. Wolters Kluwer Health 2019-03-01 /pmc/articles/PMC6831399/ /pubmed/30817598 http://dx.doi.org/10.1097/MD.0000000000014681 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Cummings, Fraser Gaya, Daniel R. Levison, Scott Subramanian, Sreedhar Owen, Glynn Rathmell, Anna Glen, Fiona Demuth, Dirk Meadowcroft, Simon Irving, Peter M. A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title | A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title_full | A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title_fullStr | A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title_full_unstemmed | A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title_short | A retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the UK: The REVIVE study |
title_sort | retrospective observational study of early experiences of vedolizumab treatment for inflammatory bowel disease in the uk: the revive study |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831399/ https://www.ncbi.nlm.nih.gov/pubmed/30817598 http://dx.doi.org/10.1097/MD.0000000000014681 |
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