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Targeted Therapies in Inflammatory Bowel Disease: Mechanisms, Comparative Evidence, and Clinical Translation

Christopher Pavel, Ana Popa, Madalina Ilie, Oana-Mihaela Plotogea, Raluca-Ioana Dascalu, Teodor Cabel, Deniz Gunsahin, Iulia Tincu, Bogdan Gaspar, Luiza Elena Pavel, Alexandra Oaie

Journal of Clinical Medicine · 2026

Vollständiger Abstract

Worum geht es in dieser Arbeit?

Inflammatory bowel disease (IBD), encompassing Crohn’s disease (CD) and ulcerative colitis (UC), is a chronic immune-mediated condition with substantial global burden and rising incidence, requiring an expanding range of advanced therapies. This focused narrative review examines the mechanistic rationale, comparative clinical evidence, and translational implications of approved and emerging targeted therapies for adult IBD. A structured literature search was conducted in PubMed, Scopus, and Web of Science for publications from January 2021 to March 2026. Thirty-eight articles were selected as the core evidence set with landmark trials and clinical guidelines added when needed for historical or practice context. Evidence was synthesised narratively, with an explicit distinction between direct head-to-head comparisons, placebo-controlled trials, indirect network comparisons, and observational data. In UC, VARSITY showed higher week-52 clinical remission and endoscopic improvement with vedolizumab than adalimumab; in CD after anti–tumour necrosis factor (anti-TNF) failure, SEQUENCE showed risankizumab noninferior to ustekinumab for week-24 clinical remission and superior for week-48 endoscopic remission. Agents targeting tumour necrosis factor-like cytokine 1A (TL1A) have shown encouraging activity in phase 2/2b trials, but long-term effectiveness and safety remain uncertain. The current evidence supports mechanism-informed rather than biomarker-defined treatment selection. Confidence in comparative conclusions is greatest when supported by direct randomised evidence, whereas observational and indirect comparisons require caution because of confounding, heterogeneity, and differences in populations and outcome definitions. Clinical translation therefore requires the integration of the disease phenotype, prior treatment exposure, safety risks, and patient preference, with objective reassessment after therapy initiation.

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Autor:innen
Christopher Pavel, Ana Popa, Madalina Ilie, Oana-Mihaela Plotogea, Raluca-Ioana Dascalu, Teodor Cabel, Deniz Gunsahin, Iulia Tincu, Bogdan Gaspar, Luiza Elena Pavel, Alexandra Oaie
Quelle
Journal of Clinical Medicine
Publikation
2026-01-01
Band / Ausgabe
Nicht angegeben
Seiten
Nicht angegeben
ISSN / ISBN
2077-0383
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Christopher Pavel, Ana Popa, Madalina Ilie, Oana-Mihaela Plotogea, Raluca-Ioana Dascalu, Teodor Cabel, Deniz Gunsahin, Iulia Tincu, Bogdan Gaspar, Luiza Elena Pavel, Alexandra Oaie (2026). Targeted Therapies in Inflammatory Bowel Disease: Mechanisms, Comparative Evidence, and Clinical Translation. Journal of Clinical Medicine. https://doi.org/10.3390/jcm15176753
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