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1000 Titel
  • Efficacy and Safety of Advanced Therapies in Moderately-to-Severely Active Ulcerative Colitis: a Systematic Review and Network Meta-analysis
1000 Autor/in
  1. Dignass, Axel |
  2. Ainsworth, Claire |
  3. Hartz, Susanne |
  4. Dunnewind, Niels |
  5. Redondo, Isabel |
  6. Sapin, Christophe |
  7. Kroep, Sonja |
  8. Halfpenny, Nicholas |
  9. Arcà, Emanuele |
  10. Hoque, Sami |
1000 Verlag Springer Healthcare
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-10-15
1000 Erschienen in
1000 Quellenangabe
  • 41(12):4446-4462
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s12325-024-03003-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11550281/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Introduction!#!This study aimed to compare the efficacy and safety of biologics and small molecules for treatment of adults with moderately-to-severely active ulcerative colitis (UC).!##!Methods!#!A systematic literature review was conducted to identify randomised controlled trials evaluating approved and emerging targeted therapies for patients with UC. A Bayesian network meta-analysis (NMA) approach was applied. Outcomes assessed included clinical response and remission, endoscopic mucosal healing, and safety.!##!Results!#!Thirty studies were included in the NMA following a feasibility assessment comparing approved induction dosing regimens and 22 studies comparing approved maintenance dosing regimens. In the biologic/Janus kinase inhibitor (JAKi)-naïve population, induction studies showed similar clinical response and remission rates across most interventions, with upadacitinib demonstrating significant improvements versus most other interventions. For maintenance studies, mirikizumab demonstrated significant improvements in clinical response and remission versus most other interventions. In the biologic/JAKi-experienced population, no significant differences were observed between most interventions in induction studies, except for significantly improved clinical response and remission for mirikizumab versus adalimumab, and upadacitinib demonstrated significant improvement versus all other interventions. Few differences between active treatments were observed in maintenance studies. In both populations, all active interventions had similar efficacy in terms of endoscopic mucosal healing in both induction and maintenance studies. Regardless of prior treatment exposure, similar rates of serious adverse events were seen across all active interventions in the induction period.!##!Conclusion!#!Among the available interventions, owing to its favourable efficacy and safety profile, mirikizumab has a relevant role in the long-term treatment of UC.
1000 Sacherschließung
lokal Colitis, Ulcerative/diagnosis [MeSH]
lokal Biologics
lokal IL-23 inhibitors
lokal Humans [MeSH]
lokal Severity of Illness Index [MeSH]
lokal Treatment Outcome [MeSH]
lokal Adalimumab/adverse effects [MeSH]
lokal Janus Kinase Inhibitors/administration
lokal Advanced therapies
lokal Bayes Theorem [MeSH]
lokal Comparative efficacy
lokal Gastrointestinal Agents/adverse effects [MeSH]
lokal Janus Kinase Inhibitors/adverse effects [MeSH]
lokal Randomized Controlled Trials as Topic [MeSH]
lokal Colitis, Ulcerative/drug therapy [MeSH]
lokal Small molecules
lokal Adalimumab/administration
lokal Biological Products/administration
lokal Biological Products/adverse effects [MeSH]
lokal Remission Induction/methods [MeSH]
lokal Original Research
lokal Ulcerative colitis
lokal Gastrointestinal Agents/administration
lokal Mirikizumab
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-9724-054X|https://frl.publisso.de/adhoc/uri/QWluc3dvcnRoLCBDbGFpcmU=|https://orcid.org/0000-0001-8475-0260|https://frl.publisso.de/adhoc/uri/RHVubmV3aW5kLCBOaWVscw==|https://frl.publisso.de/adhoc/uri/UmVkb25kbywgSXNhYmVs|https://frl.publisso.de/adhoc/uri/U2FwaW4sIENocmlzdG9waGU=|https://frl.publisso.de/adhoc/uri/S3JvZXAsIFNvbmph|https://frl.publisso.de/adhoc/uri/SGFsZnBlbm55LCBOaWNob2xhcw==|https://frl.publisso.de/adhoc/uri/QXJjw6AsIEVtYW51ZWxl|https://frl.publisso.de/adhoc/uri/SG9xdWUsIFNhbWk=
1000 Hinweis
  • DeepGreen-ID: 85fe591ab35242af8105b3499e416ac4 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. The preparation of the manuscript was funded by Eli Lilly and Company. |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer The preparation of the manuscript was funded by Eli Lilly and Company. |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6492869.rdf
1000 Erstellt am 2025-02-03T19:04:19.413+0100
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1000 beschreibt frl:6492869
1000 Zuletzt bearbeitet 2025-09-12T11:32:43.487+0200
1000 Objekt bearb. Fri Sep 12 11:32:43 CEST 2025
1000 Vgl. frl:6492869
1000 Oai Id
  1. oai:frl.publisso.de:frl:6492869 |
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