Evidence map›Paper›PMID 41023875›Full record

ArticleBMC gastroenterology2025

Direct conversion of ustekinumab therapy is more beneficial than infliximab-optimized therapy in patients with Crohn's disease who develop secondary loss of response to infliximab.

Lin Li, Xuemei Xu, Jing Wang, Li Xie, Xiaoping Niu

Abstract readComparative Study
In one paragraph

Article in BMC gastroenterology, 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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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lin Li *Departments of Gastroenterology, The First Affiliated Hospital of Wannan Medical College, Wuhu, 241001, People's Republic of China.
Xuemei Xu *Departments of Gastroenterology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230000, People's Republic of China.
Jing Wang *Departments of Gastroenterology, The First Affiliated Hospital of Wannan Medical College, Wuhu, 241001, People's Republic of China.
Li XieDepartments of Gastroenterology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230000, People's Republic of China. 1878818433@qq.com.
Xiaoping NiuDepartments of Gastroenterology, The First Affiliated Hospital of Wannan Medical College, Wuhu, 241001, People's Republic of China. 47440311@qq.com.

Funding

Anhui Province clinical medical research transformation project No.202427b10020077Introduction of Talents Special Research Fund Project No.YR202427Key project of Anhui University Scientific Research Program No.2024AH051969Key Research Project of Wannan Medical College No.WK2022ZF03
6 · The paper itself

Abstract

backgroundFor patients with Crohn's disease (CD) who develop secondary loss of response (SLR) to infliximab (IFX), it remains unclear whether IFX optimization or direct conversion to ustekinumab (UST) offers better outcomes. This study aimed to identify risk factors for IFX optimization failure and to compare the clinical efficacy of IFX optimization versus UST conversion.

methodsWe retrospectively analyzed clinical data from patients with CD admitted to the First Affiliated Hospital of Wannan Medical College and the First Affiliated Hospital of the University of Science and Technology of China between January 2017 and January 2025. Rates of clinical, steroid-free, and endoscopic remission were assessed. Univariate and multivariate analyses were performed to identify independent risk factors for IFX optimization failure.

resultsIn total, 65 patients with CD who developed SLR to IFX were included. The patients were divided into three groups: IFX optimization success (Group 1), IFX optimization failure followed by UST (Group 2), and direct UST conversion (Group 3). Of the 28 patients who received IFX optimization, only 6 achieved success, yielding a failure rate of 78.6%. Multivariate logistic regression showed that a baseline albumin concentration of < 40 g/L was an independent predictor of IFX optimization failure (p = 0.047, odds ratio: 15.00, 95% confidence interval: 1.031-218.300). When comparing UST-treated groups, the rate of clinical response at week 6 was significantly higher in Group 3 than in Group 2 (35.1% vs. 9.1%, p = 0.039). By week 52, clinical remission rates were similar (86.4% vs. 89.2%, p > 0.05).

conclusionsGiven the high failure rate of IFX optimization, direct conversion to UST may provide greater benefit and reduce treatment costs in patients with CD who develop SLR to IFX.

Indexed as

Crohn DiseaseGastrointestinal AgentsInfliximabUstekinumabAdultFemaleHumansMaleMiddle AgedRemission InductionRetrospective StudiesRisk FactorsTreatment FailureTreatment OutcomeYoung AdultGastrointestinal AgentsInfliximabUstekinumabConversion therapyCrohn’s diseaseInfliximabOptimal therapyUstekinumab

Identifiers

PMID41023875
PMCPMC12481795

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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.