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Raising the bar in ulcerative colitis management.

Authors :
Fanizzi F
Allocca M
Fiorino G
Zilli A
Furfaro F
Parigi TL
Peyrin-Biroulet L
Danese S
D'Amico F
Source :
Therapeutic advances in gastroenterology [Therap Adv Gastroenterol] 2024 Nov 24; Vol. 17, pp. 17562848241273066. Date of Electronic Publication: 2024 Nov 24 (Print Publication: 2024).
Publication Year :
2024

Abstract

Ulcerative colitis (UC) is a chronic inflammatory bowel disease characterized by growing incidence and prevalence around the world in the last few decades. The range of available existing treatment and strategies for its management is being implemented. Given the introduction of newly developed molecules and the lack of specific guidelines, drug positioning may represent a tough clinical challenge. UC management is mostly medical, and it has been shifting toward a more personalized approach with the aim to create a tailored strategy depending on the patient's profile. A treat-to target strategy seems to be the best approach to reach disease control as it allows to carry out therapeutic choices based on objective and specific parameters: histological, ultrasonographic, and molecular targets may add to the already used clinical, endoscopic, and biochemical targets. In addition, dual-targeted therapy has emerged as an attractive therapeutic strategy for patients not achieving remission. This review aims to provide an overview of the available strategies to raise the bar in UC.<br />Competing Interests: The article processing charges for this publication have been waived under an educational grant from Takeda Pharmaceuticals Limited. F.D. has served as a speaker for Sandoz, Janssen, Galapagos, Omega Pharma, Takeda, and Tillotts; he also served as a consultant for Ferring and as an advisory board member for Galapagos, Abbvie, and Nestlè. S.D. has served as a speaker, consultant, and advisory board member for Schering-Plough, AbbVie, Actelion, Alphawasserman, AstraZeneca, Cellerix, Cosmo Pharmaceuticals, Ferring, Genentech, Grunenthal, Johnson and Johnson, Millenium Takeda, MSD, Nikkiso Europe GmbH, Novo Nordisk, Nycomed, Pfizer, Pharmacosmos, UCB Pharma, and Vifor. L.P.-B. declares personal fees from Galapagos, AbbVie, Janssen, Genentech, Ferring, Tillots, Celltrion, Takeda, Pfizer, Index Pharmaceuticals, Sandoz, Celgene, Biogen, Samsung Bioepis, Inotrem, Allergan, MSD, Roche, Arena, Gilead, Amgen, BMS, Vifor, Norgine, Mylan, Lilly, Fresenius Kabi, OSE Immunotherapeutics, Enthera, Theravance, Pandion Therapeutics, Gossamer Bio, Viatris, Thermo Fisher; grants from Abbvie, MSD, Takeda, Fresenius Kabi; stock options from CTMA. F.F. received consulting fees from Amgen, AbbVie, and lecture fees from Janssen and Pfizer. G.F. received consultancy fees from Ferring, MSD, AbbVie, Takeda, Janssen, Amgen, Sandoz, Samsung Bioepis, and Celltrion. M.A. has received consulting fees from Nikkiso Europe, Mundipharma, Janssen, AbbVie, Pfizer, and Ferring. The other authors have no conflict of interest to declare.<br /> (© The Author(s), 2024.)

Details

Language :
English
ISSN :
1756-283X
Volume :
17
Database :
MEDLINE
Journal :
Therapeutic advances in gastroenterology
Publication Type :
Academic Journal
Accession number :
39600566
Full Text :
https://doi.org/10.1177/17562848241273066