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Efficacy and Safety of Advanced Therapies for Moderately to Severely Active Ulcerative Colitis at Induction and Maintenance: An Indirect Treatment Comparison Using Bayesian Network Meta-analysis.
Panaccione, Remo; Collins, Eric B; Melmed, Gil Y; Vermeire, Severine; Danese, Silvio; Higgins, Peter D R; Kwon, Christina S; Zhou, Wen; Ilo, Dapo; Sharma, Dolly; Sanchez Gonzalez, Yuri; Wang, Si-Tien.
  • Panaccione R; Inflammatory Bowel Disease Unit, Division of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, Canada.
  • Collins EB; Medicus Economics LLC, Milton, Massachusetts, USA.
  • Melmed GY; Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Vermeire S; Department of Gastroenterology & Hepatology, University Hospital Leuven, KU Leuven, Leuven, Belgium.
  • Danese S; Gastroenterology and Endoscopy, IRCCS Ospedale San Raffaele, Department of Gastroenterology, University Vita-Salute San Raffaele, Milan, Italy.
  • Higgins PDR; Department of Medicine, Division of Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA.
  • Kwon CS; Cytel, Inc., Waltham, Massachusetts, USA.
  • Zhou W; AbbVie Inc., North Chicago, Illinois, USA.
  • Ilo D; AbbVie Inc., North Chicago, Illinois, USA.
  • Sharma D; AbbVie Inc., North Chicago, Illinois, USA.
  • Sanchez Gonzalez Y; AbbVie Inc., North Chicago, Illinois, USA.
  • Wang ST; Medicus Economics LLC, Milton, Massachusetts, USA.
Crohns Colitis 360 ; 5(2): otad009, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36998249
ABSTRACT

Background:

Given rapid innovation in advanced therapies for moderately to severely active ulcerative colitis (UC), we investigated their comparative efficacy and safety during induction and maintenance through network meta-analysis.

Methods:

Using Bayesian methods, endpoints of clinical remission and clinical response per Full Mayo score, and endoscopic improvement were assessed in bio-naive and -exposed populations. Safety was assessed in overall populations by all adverse events (AEs), serious AEs, discontinuation due to AEs, and serious infections. Phase 3 randomized controlled trials were identified via systematic literature review, including the following advanced therapies infliximab, adalimumab, vedolizumab, golimumab, tofacitinib, ustekinumab, filgotinib, ozanimod, and upadacitinib. Random effects models were used to address between-study heterogeneity. Intent-to-treat (ITT) efficacy rates were calculated by adjusting maintenance outcomes by likelihood of induction response.

Results:

Out of 48 trials identified, 23 were included. Across all outcomes and regardless of prior biologic exposure, ITT efficacy rates were highest for upadacitinib, owing to its highest ranking for all efficacy outcomes in induction and for all but clinical remission during maintenance among bio-naive induction responders. For all advanced therapies versus placebo, there were no significant differences in serious AEs or serious infections across therapies. For all AEs, golimumab had higher odds versus placebo during maintenance; for discontinuation due to AEs, upadacitinib had lower odds versus placebo during induction, while ustekinumab and vedolizumab had lower odds versus placebo during maintenance.

Conclusions:

Upadacitinib may be the most efficacious therapy for moderately to severely active UC based on ITT analyses, with similar safety across advanced therapies.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Año: 2023 Tipo del documento: Article