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Ustekinumab Versus Anti-tumour Necrosis Factor Alpha Agents as Second-Line Biologics in Crohn's Disease
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.ORCID iD: 0000-0002-1046-383x
Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Örebro University, School of Medical Sciences. Department of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID iD: 0000-0002-4923-3169
Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Division of Gastroenterology, Department of Specialist Medicine, Danderyd Hospital, Stockholm, Sweden.
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2023 (English)In: Digestive Diseases and Sciences, ISSN 0163-2116, E-ISSN 1573-2568, Vol. 68, no 7, p. 3119-3128Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: There are little data on positioning biologics in Crohn's disease (CD). AIMS: We 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.

METHODS: We 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.

RESULTS: Some 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).

CONCLUSION: Based 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.

Place, publisher, year, edition, pages
Springer-Verlag New York, 2023. Vol. 68, no 7, p. 3119-3128
Keywords [en]
Anti-TNF, Comparative effectiveness, Comparative safety, Crohn’s disease, Population-based study, Ustekinumab
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-105110DOI: 10.1007/s10620-023-07897-2ISI: 000952916200002PubMedID: 36929241Scopus ID: 2-s2.0-85150157990OAI: oai:DiVA.org:oru-105110DiVA, id: diva2:1745166
Funder
Örebro UniversityRegion Örebro County, OLL-836791Swedish Society of Medicine, SLS-789611Stockholm County Council, 20170720 20190638Karolinska Institute, 20170720 20190638Swedish Research Council, 2020-02002
Note

Funding agencies:

Johnson & Johnson USA Janssen Biotech Inc CNTO1275CRD0005

Stockholm Region Clinical Postdoctoral Researcher Grant

Strategic Research Area Epidemiology program at Karolinska Institutet

 

Available from: 2023-03-22 Created: 2023-03-22 Last updated: 2023-12-08Bibliographically approved

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Eriksson, CarlKarlqvist, SaraBergemalm, DanielLudvigsson, Jonas F.Halfvarson, Jonas

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