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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...

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Autores principales: Cummings, Fraser, Gaya, Daniel R., Levison, Scott, Subramanian, Sreedhar, Owen, Glynn, Rathmell, Anna, Glen, Fiona, Demuth, Dirk, Meadowcroft, Simon, Irving, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
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.
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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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