Evidence map›Paper›PMID 42298310›Full record

ArticleAlimentary pharmacology & therapeutics2026

Comparative Real-World Effectiveness of Anti-TNF, Ustekinumab and Vedolizumab in Crohn's Disease Over 24 Months: A Pooled Analysis From the Prospective UMBRELLA-IBD Registry in Germany.

Arne Bokemeyer, Florian Tran, Sandra Plachta-Danielzik, Elena Gilman, Thomas Wenske, Matthew Gaskins, Stefan Schreiber, Bernd Bokemeyer

Abstract readComparative Study
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2026. 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. Review
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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

8 authors.

Arne BokemeyerDepartment for Gastroenterology, Diabetology and Palliative Care, Bonifatius Hospital Lingen, Lingen, Germany.ORCID https://orcid.org/0000-0002-4238-751X
Florian TranClinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID https://orcid.org/0000-0002-3735-9872
Sandra Plachta-DanielzikCompetence Network IBD, Kiel, Germany.ORCID https://orcid.org/0000-0002-1945-4198
Elena GilmanCompetence Network IBD, Kiel, Germany.ORCID https://orcid.org/0009-0004-6079-0240
Thomas WenskeCompetence Network IBD, Kiel, Germany.ORCID https://orcid.org/0009-0003-0491-5670
Matthew GaskinsIndependent Public Health Researcher, Madrid, Spain.ORCID https://orcid.org/0000-0001-6436-2703
Stefan SchreiberClinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID https://orcid.org/0000-0002-6807-9822
Bernd BokemeyerClinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID https://orcid.org/0000-0003-2016-6991

Funding

Competence Network IBD
6 · The paper itself

Abstract

backgroundReal-world evidence is needed to understand the comparative effectiveness of biologics in Crohn's disease (CD) under routine-care conditions. We conducted a pooled analysis of individual patient data from prospective German CD registries (BioCrohn, RUN-CD, VEDO-IBD) in the UMBRELLA-IBD data warehouse.

methodsWe included 1567 adults with CD who initiated anti-TNF therapy (adalimumab or infliximab), ustekinumab or vedolizumab. The main outcome was clinical remission (CR) at 24 months (HBI ≤ 4). Additional outcomes included HBI, EQ-VAS and treatment persistence over time. Between-group comparisons used propensity-score-based inverse probability of treatment weighting.

resultsAfter weighting, CR following induction was observed in a slightly higher proportion of patients initiating anti-TNF therapy (74.5%) than ustekinumab (69.4%) or vedolizumab (65.3%) (p = 0.035). Clinical response was 77.9%, 73.5% and 67.8%, respectively (p = 0.015). At 24 months, CR rates were similar in magnitude (anti-TNF, 53.4%; ustekinumab, 63.5%; vedolizumab, 58.7%) but were higher with ustekinumab than anti-TNF (p = 0.004). Over 24 months, treatment persistence differed (log-rank p < 0.001) and was highest for adalimumab (81.4%), lowest for infliximab (66.6%), and intermediate for ustekinumab (78.6%) and vedolizumab (76.9%). HBI decreased and remained low, and EQ-VAS improved, with no relevant between-group differences.

conclusionOverall effectiveness in CD was high, with only small differences between biologic therapies. At the end of induction, CR was slightly higher with anti-TNF therapy than with vedolizumab, whereas at 24 months it was slightly higher with ustekinumab than with anti-TNF. Marked differences in treatment persistence among the evaluated biologics suggest that persistence as an endpoint is not fully explained by CR alone.

Indexed as

Antibodies, Monoclonal, HumanizedCrohn DiseaseGastrointestinal AgentsTumor Necrosis Factor-alphaUstekinumabAdalimumabAdultFemaleGermanyHumansInfliximabMaleMiddle AgedProspective StudiesRegistriesRemission InductionAdalimumabAntibodies, Monoclonal, HumanizedGastrointestinal AgentsInfliximabTumor Necrosis Factor-alphaUstekinumabvedolizumabbiologic therapyclinical remissionCrohn's diseasepropensity score weightingreal‐world evidencetreatment persistence

Identifiers

PMID42298310
PMCPMC13511377

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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.