Evidence map›Paper›PMID 36929241›Full record

ArticleDigestive diseases and sciences2023

Ustekinumab Versus Anti-tumour Necrosis Factor Alpha Agents as Second-Line Biologics in Crohn's Disease.

Carl Eriksson, Jonas Söderling, Sara Karlqvist, Gabriella Bröms, Åsa H Everhov, Daniel Bergemalm, Jonas F Ludvigsson, SWIBREG study group, Ola Olén, Jonas Halfvarson

Open access · hybridAbstract read
In one paragraph

Article in Digestive diseases and sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Cost calculation model of introducing Upadacitinib and Risankizumab for adult ulcerative colitis and Crohn's disease in the Kingdom of Saudi Arabia.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association · 2026
    Article
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Carl ErikssonDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden. carl.eriksson@regionorebrolan.se.ORCID 0000-0002-1046-383X
Jonas SöderlingClinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Sara KarlqvistDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Gabriella BrömsClinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Åsa H EverhovClinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Daniel BergemalmDepartment of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Jonas F LudvigssonDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
SWIBREG study group
Ola Olén *Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Jonas Halfvarson *Department of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Örebro University · SEKarolinska Institutet · SEDanderyds sjukhus · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere are little data on positioning biologics in Crohn's disease (CD).

aimsWe aimed to assess the comparative effectiveness and safety of ustekinumab vs tumour necrosis factor-alpha (anti-TNF) agents after first-line treatment with anti-TNF in CD.

methodsWe used Swedish nationwide registers to identify patients with CD, exposed to anti-TNF who initiated second-line biologic treatment with ustekinumab or second-line anti-TNF therapy. Nearest neighbour 1:1 propensity score matching (PSM) was used to balance the groups. The primary outcome was 3-year drug survival used as a proxy for effectiveness. Secondary outcomes included drug survival without hospital admission, CD-related surgery, antibiotics, hospitalization due to infection and exposure to corticosteroids.

resultsSome 312 patients remained after PSM. Drug survival at 3 years was 35% (95% CI 26-44%) in ustekinumab compared to 36% (95% CI 28-44%) in anti-TNF-treated patients (p = 0.72). No statistically significant differences were observed between the groups in 3-year survival without hospital admission (72% vs 70%, p = 0.99), surgery (87% vs 92%, p = 0.17), hospital admission due to infection (92% vs 92%, p = 0.31) or prescription of antibiotics (49% vs 50%, p = 0.56). The proportion of patients continuing second-line biologic therapy did not differ by reason for ending first-line anti-TNF (lack of response vs intolerance) or by type of first-line anti-TNF (adalimumab vs infliximab).

conclusionBased on data from Swedish routine care, no clinically relevant differences in effectiveness or safety of second-line ustekinumab vs anti-TNF treatment were observed in patients with CD with prior exposure to anti-TNF.

Indexed as

Biological ProductsCrohn DiseaseAdalimumabAntibodies, Monoclonal, HumanizedBiological FactorsHumansInfliximabNecrosisTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsUstekinumabAdalimumabAntibodies, Monoclonal, HumanizedBiological FactorsBiological ProductsInfliximabTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsUstekinumabAnti-TNFComparative effectivenessComparative safetyCrohn’s diseasePopulation-based studyUstekinumab

Identifiers

PMID36929241
PMCPMC10293383
OpenAlexW4327683939

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.