Evidence map›Paper›PMID 40515784›Full record

ArticleDigestive diseases and sciences2025

Patients with Crohn's Disease and Ileostomy Can Respond to Upadacitinib.

Lauren Loeb, Francis A Farraye, Sheena Crosby, Edward V Loftus, Christina Ha, Jami A Kinnucan, Michael F Picco, Jana G Hashash

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Article in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Lauren LoebDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Francis A FarrayeDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Sheena CrosbyDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Edward V LoftusDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Christina HaDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ, USA.
Jami A KinnucanDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Michael F PiccoDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Jana G HashashDivision of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA. AlHashash.Jana@mayo.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have established a role for Janus kinase (JAK) inhibitors in the management of patients with inflammatory bowel disease. However, these studies excluded patients with an ileostomy.

aimWe sought to evaluate the clinical response of patients with Crohn's disease (CD) and ileostomy who were treated with upadacitinib.

methodsThis retrospective study included patients with CD who had an ileostomy secondary to medically refractory CD and who were treated with upadacitinib. Patients who underwent ileostomy takedown and continued taking upadacitinib were analyzed separately from patients with an ileostomy throughout upadacitinib treatment duration. The primary endpoint was clinical response defined by either continuation or discontinuation of upadacitinib. The secondary endpoint was identifying variables that lead to discontinuation of upadacitinib.

resultsA total of 48 patients, between the ages of 17-70 years met our inclusion criteria of having CD, an ileostomy, and upadacitinib use after ileostomy creation. Of the 48 patients, 32 (67%) had clinical improvement in CD activity with upadacitinib use based on review of clinical documentation. Upadacitinib was discontinued in 16 patients (33%) for various reasons including refractory symptoms related to CD, deep vein thrombosis, anemia/leukopenia, insurance denial, pregnancy planning, headache/back pain, or squamous cell carcinoma of the skin.

conclusionWe evaluated the efficacy of upadacitinib in patients with CD and ileostomy. Two-thirds of our cohort experienced improvement in CD-related symptoms with upadacitinib use. Further studies are needed to evaluate if altered gastrointestinal anatomy significantly impacts absorption and efficacy of upadacitinib in patients with CD.

Indexed as

Crohn DiseaseHeterocyclic Compounds, 3-RingIleostomyJanus Kinase InhibitorsAdolescentAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeYoung AdultHeterocyclic Compounds, 3-RingJanus Kinase InhibitorsupadacitinibCrohn’s diseaseIleostomyJanus kinase inhibitorsUpadacitinib

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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.