Evidence map›Paper›PMID 39659234›Full record

ArticleJournal of Crohn's & colitis2025

Tofacitinib Versus Vedolizumab Among Bio-naive Patients With Ulcerative Colitis: A Real-World Propensity-Weighted Comparison.

Beatriz Gros, Nathan Constantine-Cooke, Jake Kennedy, Alexander T Elford, Claire O'Hare, Colin Noble, Gareth-Rhys Jones, Ian D Arnott, Charlie W Lees, Nikolas Plevris

Abstract readComparative Study
In one paragraph

Article in Journal of Crohn's & colitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

10 authors.

Beatriz GrosEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.ORCID 0000-0002-5628-313X
Nathan Constantine-CookeCentre for Genomics and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK.ORCID 0000-0002-4437-8713
Jake KennedyEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.ORCID 0000-0003-3860-3977
Alexander T ElfordEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.ORCID 0000-0001-6144-1369
Claire O'HareEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.
Colin NobleEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.
Gareth-Rhys JonesEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.
Ian D ArnottEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.
Charlie W LeesEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.
Nikolas PlevrisEdinburgh IBD Unit, Western General Hospital, Edinburgh, UK.ORCID 0000-0002-3229-8759

Funding

Australian Commonwealth GovernmentClinical Research Career Development FellowshipUKRI MR/S034919/1Welcome Trust
6 · The paper itself

Abstract

BACKGROUND AND

aimsOver the last decade, treatment options for moderate-to-severe ulcerative colitis (UC) have expanded. However, comparative studies between these agents are limited, especially among biologic-naive patients. We aimed to compare the persistence, effectiveness, and safety of tofacitinib and vedolizumab as the first advanced treatment for patients with UC.

methodsPatients who received either tofacitinib or vedolizumab as their first advanced therapy for UC in NHS Lothian were included. We used inverse probability of treatment weighting. The probability of treatment assignment was calculated via logistic regression using age, sex, UC duration, Montreal extent, C-reactive protein, concomitant corticosteroids, and partial Mayo score at drug commencement.

resultsWe included n = 158 patients, of whom n = 81 (51.3%) received vedolizumab and n = 77 (48.7%) tofacitinib. Median follow-up for vedolizumab patients was 3.1 years (interquartile range [IQR] 1.6-4.8) and for tofacitinib patients 1.5 years (IQR 0.3-2.3). The cohort was 59.5% male with a median age of 41.1 years (IQR 31.5-51.8). At 2 years, vedolizumab persistence was superior to tofacitinib (p = 0.005). At Weeks 12 and 52, clinical, biochemical, and fecal biomarker steroid-free remission were comparable between groups. Primary nonresponse and secondary loss of response were 9.9% and 17.3% for vedolizumab and 23.4% and 13% for tofacitinib, respectively. The frequency of adverse events was comparable (11 [13.6%] vedolizumab vs 19 [24.7%] tofacitinib, p = 0.629).

conclusionsWe found that the persistence and tolerability of vedolizumab were superior to tofacitinib in bio-naive UC, although the rates of clinical and biomarker remission were comparable. These data may help inform the positioning of advanced therapy.

Indexed as

Antibodies, Monoclonal, HumanizedColitis, UlcerativeGastrointestinal AgentsPiperidinesPyrimidinesAdultFemaleHumansMaleMiddle AgedPropensity ScoreTreatment OutcomeAntibodies, Monoclonal, HumanizedGastrointestinal AgentsPiperidinesPyrimidinestofacitinibvedolizumabbiologicsreal-world datasmall moleculeUlcerative colitis

Identifiers

PMID39659234
PMCPMC12260496

What OpenQuestion holds

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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.