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Upadacitinib Is Associated with the Lowest Risk of Treatment Failure Among Advanced Therapies for Ulcerative Colitis: A Real-World Administrative Claims Study.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association

Cure8 research brief

Upadacitinib Is Associated with the Lowest Risk of Treatment Failure Among Advanced Therapies for Ulcerative Colitis: A Real-World Administrative Claims Study.

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Why This Matters

This large real-world study found upadacitinib was associated with lower risk of treatment failure and more corticosteroid-free stability compared with several other advanced therapies for ulcerative colitis — information that may influence treatment discussions for patients and clinicians.

Who Should Pay Attention

Adults with ulcerative colitis; clinicians prescribing advanced therapies; researchers in IBD comparative effectiveness.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

A large US administrative-claims study compared real-world outcomes for several advanced therapies used to treat ulcerative colitis: infliximab, adalimumab, vedolizumab, ustekinumab, tofacitinib, and upadacitinib.

The primary outcome was time to treatment failure (IBD-related hospitalization, surgery, or a new corticosteroid prescription >90 days after starting therapy); treatment discontinuation and switching were censored.

After statistical adjustment, upadacitinib was associated with the lowest risk of treatment failure versus each other drug evaluated and had the highest proportion of quarters spent in corticosteroid-free disease stability. The study used a large US claims database and applied propensity-score weighting and competing risk methods to address confounding.

Outcomes reflect administrative claims (hospitalization, surgery, new steroid prescriptions) rather than clinical measures such as endoscopic healing or patient-reported symptoms. This is an observational, non-randomized analysis of real-world data. While the authors adjusted for many confounders, residual confounding and treatment-selection bias may remain.

The results show associations, not cause-and-effect, and may be influenced by prescribing patterns, differences in patient populations, or unmeasured disease severity.

Keep In Mind

Observational claims data can show associations but cannot prove causation. Outcomes were derived from administrative claims (hospitalizations, surgeries, steroid prescriptions) rather than direct clinical or endoscopic measures; residual confounding is possible.

Source Details

Review the original publication for the complete reporting, methods, and context.

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Research paper Evidence type derived from source or registry metadata.
PublicationClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
AuthorsMarianne Hupé, Dhruv Ahuja, Kuan-Hung Yeh +9 more
InstitutionDivision of Gastroenterology, Western University, London, Ontario, Canada; Univ. Grenoble Alpes / Hepato-Gastroenterology and Digestive Oncology department, CHU Grenoble Alpes / Institute for Advanced Biosciences, CNRS UMR 5309-INSERM U1209, Grenoble, France.
Study typeJournal article
Indexed viaPubMed
Source typeResearch paper
PublishedSep 29, 2026, 12:00 AM
Content availableJournal abstract

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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