Evidence map›Paper›PMID 41642870›Full record

ReviewPLOS digital health2026

Optimizing vedolizumab therapy in ulcerative colitis: A critical synthesis of trial evidence and the emerging role of artificial intelligence.

Alfadl Abdulfattah

Abstract readReview
In one paragraph

Review in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Alfadl AbdulfattahDepartment of Internal Medicine, College of Medicine, Jazan University, Jazan, Saudi Arabia.ORCID https://orcid.org/0000-0002-2325-5044

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVedolizumab, a monoclonal antibody targeting the α4β7 integrin, offers gut-selective immunosuppression and represents a cornerstone biologic therapy for moderate-to-severe ulcerative colitis (UC). While pivotal randomized controlled trials (RCTs) have established its efficacy, a substantial subset of patients experience primary non-response. This variability presents significant clinical challenges, including patient morbidity and healthcare costs associated with cycling through ineffective therapies, underscoring an urgent need for personalized treatment strategies.

objectivesThis review aims to critically reappraise the foundational RCT evidence supporting vedolizumab use in UC, examining both strengths and limitations, and providing a comprehensive analysis of how artificial intelligence (AI), particularly machine learning (ML), can be leveraged to optimize vedolizumab treatment selection, predict outcomes, and personalize management.

methodsA systematic literature search was performed across PubMed, Scopus, and Web of Science databases. The review synthesized data from key Phase III trials (GEMINI 1, VARSITY), long-term extension safety studies, relevant meta-analyses summarizing efficacy and safety, and pertinent studies investigating the application of AI and ML techniques within inflammatory bowel disease management. The search included terms such as vedolizumab, UC, AI, and predictive modeling.

findingsLandmark trials confirmed vedolizumab's superiority over placebo for inducing and maintaining remission, with week 52 clinical remission rates reaching 41.8% in the GEMINI 1 trial. Concurrently, emerging AI/ML models, integrating complex patient data, show considerable promise in predicting biologic response with high accuracy, with some models achieving an area under the curve (AUC) of 0.82 (95% CI 0.78-0.86). Neural networks have demonstrated an accuracy of approximately 79% in specific predictive contexts.

conclusionsThe strategic integration of AI-driven predictive analytics with vedolizumab's clinical and pharmacodynamic data represents a pivotal next step towards achieving true precision medicine in UC.

Identifiers

PMID41642870
PMCPMC12875509

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.