Evidence map›Paper›PMID 41081067›Full record

ArticlePrzeglad gastroenterologiczny2025

Evaluation of the clinical utility of measuring serum infliximab and vedolizumab concentrations during monitoring of biologic therapy in patients with inflammatory bowel disease.

Beata Kotowicz, Magdalena Chojnacka, Małgorzata Fuksiewicz, Piotr Kucha, Edyta Zagórowicz

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In one paragraph

Article in Przeglad gastroenterologiczny, 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

What it found

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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.

Beata KotowiczCancer Biomarker and Cytokines Laboratory Unit, The Maria Sklodowska-Curie National Research Institute of Oncology Warsaw, Poland.
Magdalena ChojnackaCancer Biomarker and Cytokines Laboratory Unit, The Maria Sklodowska-Curie National Research Institute of Oncology Warsaw, Poland.
Małgorzata FuksiewiczCancer Biomarker and Cytokines Laboratory Unit, The Maria Sklodowska-Curie National Research Institute of Oncology Warsaw, Poland.
Piotr KuchaDepartment of Gastroenterology, The Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Edyta ZagórowiczDepartment of Gastroenterology, The Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Infliximab (IFX) and vedolizumab (VDZ) are monoclonal antibodies used for the treatment of inflammatory bowel diseases (IBD), such as Crohn's disease (CD) and ulcerative colitis (UC). The concentration of biologic drugs must be high enough for a therapeutic response. Aim: To evaluate the association of VDZ or IFX concentrations with the clinical condition of patients with IBD during therapy. Material and methods: We examined 82 patients with IBD treated with VDZ or IFX. Blood samples were before the administration of the drug dose. Serum drugs were determined by ELISA with RIDASCREEN kits from R-Biopharm AG. Results: The highest median serum VDZ concentrations were observed in patients with UC and endoscopic response or remission. The median serum VDZ concentration during the maintenance phase in patients with endoscopic remission remained at similar levels, while in patients without remission, a decrease was shown. Additionally, analysis of VDZ concentrations in the group of patients without endoscopic remission showed a significant decrease in drug concentration in the maintenance phase compared the induction phase ( Conclusions: The sustained serum concentrations of VDZ in patients with IBD determined in the maintenance phase confirmed a positive response to this therapy, which in practice may have significance in optimising the dosage of biological treatment.

Indexed as

biologic treatmentdrug monitoringinflammatory bowel diseasemonoclonal antibodies

Identifiers

PMID41081067
PMCPMC12508381

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