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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.
Afiliação
  • Cummings F; Department of Gastroenterology, University Hospital Southampton NHS Foundation Trust, Southampton.
  • Gaya DR; Gastroenterology Unit, Glasgow Royal Infirmary, NHS Greater Glasgow and Clyde, Glasgow.
  • Levison S; Department of Gastroenterology, Manchester Royal Infirmary, Central Manchester University Hospitals NHS Foundation Trust, Manchester.
  • Subramanian S; Department of Gastroenterology, Royal Liverpool University Hospital, Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool.
  • Owen G; Takeda UK Ltd, High Wycombe, UK. Current address: Takeda Pharmaceuticals International AG, Zurich, Switzerland.
  • Rathmell A; Takeda UK Ltd, High Wycombe, UK. Current address: Takeda Pharmaceuticals International AG, Zurich, Switzerland.
  • Glen F; pH Associates, Marlow.
  • Demuth D; Evidence and Value Generation, Takeda Development Centre Europe Ltd.
  • Meadowcroft S; Takeda UK Ltd, High Wycombe, UK. Current address: Takeda Pharmaceuticals International AG, Zurich, Switzerland.
  • Irving PM; IBD Unit, St Thomas' Hospital, Guys and St Thomas' NHS Foundation Trust, London, UK.
Medicine (Baltimore) ; 98(9): e14681, 2019 Mar.
Article em En | MEDLINE | ID: mdl-30817598
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Colite Ulcerativa / Doença de Crohn / Anticorpos Monoclonais Humanizados Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Colite Ulcerativa / Doença de Crohn / Anticorpos Monoclonais Humanizados Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2019 Tipo de documento: Article