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Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing

BACKGROUND: Ustekinumab (UST) is indicated for the treatment of Crohn’s disease (CD) and Ulcerative Colitis (UC). Despite having shown clinical effectiveness in the real world, some patients may lose response over time or need a higher dose to achieve it. In this context, UST intravenous (IV) mainte...

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Autores principales: Argüelles-Arias, Federico, Valdés Delgado, Teresa, Maldonado Pérez, Belén, González Antuña, Jaime, Castro Laria, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467174/
https://www.ncbi.nlm.nih.gov/pubmed/37655058
http://dx.doi.org/10.1177/17562848231191670
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author Argüelles-Arias, Federico
Valdés Delgado, Teresa
Maldonado Pérez, Belén
González Antuña, Jaime
Castro Laria, Luisa
author_facet Argüelles-Arias, Federico
Valdés Delgado, Teresa
Maldonado Pérez, Belén
González Antuña, Jaime
Castro Laria, Luisa
author_sort Argüelles-Arias, Federico
collection PubMed
description BACKGROUND: Ustekinumab (UST) is indicated for the treatment of Crohn’s disease (CD) and Ulcerative Colitis (UC). Despite having shown clinical effectiveness in the real world, some patients may lose response over time or need a higher dose to achieve it. In this context, UST intravenous (IV) maintenance has been proposed. OBJECTIVES: The primary endpoint of our study was to evaluate the efficacy and safety of maintenance IV UST treatment in Inflammatory Bowel Disease (IBD) patients who present with partial response or loss of response to subcutaneous (SC) UST. DESIGN: We performed a monocentric observational retrospective study including patients with active IBD on maintenance treatment with IV UST. METHODS: The clinical response and remission was analyzed at week 12, defined as either Harvey–Bradshaw Index ⩽ 4 for CD or partial Mayo Score ⩽ 2 for UC. The reduction of objective markers of disease activity, fecal calprotectin, and C-reactive protein was evaluated. Moreover, UST trough levels were measured pre- and post-UST IV maintenance and any adverse events were assessed. RESULTS: We included 23 patients. Clinical remission at week 12 was achieved by 43.5% of the patients. The proportion of patients in clinical response after 12 weeks on UST IV maintenance was 82.6%. After a median follow-up of 9.3 months all patients remained on IV UST maintenance. No adverse events were recorded in any patient for the duration of the study. CONCLUSIONS: IV UST maintenance treatment was able to recapture response in most of the patients who had lost response to SC maintenance.
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spelling pubmed-104671742023-08-31 Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing Argüelles-Arias, Federico Valdés Delgado, Teresa Maldonado Pérez, Belén González Antuña, Jaime Castro Laria, Luisa Therap Adv Gastroenterol Original Research BACKGROUND: Ustekinumab (UST) is indicated for the treatment of Crohn’s disease (CD) and Ulcerative Colitis (UC). Despite having shown clinical effectiveness in the real world, some patients may lose response over time or need a higher dose to achieve it. In this context, UST intravenous (IV) maintenance has been proposed. OBJECTIVES: The primary endpoint of our study was to evaluate the efficacy and safety of maintenance IV UST treatment in Inflammatory Bowel Disease (IBD) patients who present with partial response or loss of response to subcutaneous (SC) UST. DESIGN: We performed a monocentric observational retrospective study including patients with active IBD on maintenance treatment with IV UST. METHODS: The clinical response and remission was analyzed at week 12, defined as either Harvey–Bradshaw Index ⩽ 4 for CD or partial Mayo Score ⩽ 2 for UC. The reduction of objective markers of disease activity, fecal calprotectin, and C-reactive protein was evaluated. Moreover, UST trough levels were measured pre- and post-UST IV maintenance and any adverse events were assessed. RESULTS: We included 23 patients. Clinical remission at week 12 was achieved by 43.5% of the patients. The proportion of patients in clinical response after 12 weeks on UST IV maintenance was 82.6%. After a median follow-up of 9.3 months all patients remained on IV UST maintenance. No adverse events were recorded in any patient for the duration of the study. CONCLUSIONS: IV UST maintenance treatment was able to recapture response in most of the patients who had lost response to SC maintenance. SAGE Publications 2023-08-24 /pmc/articles/PMC10467174/ /pubmed/37655058 http://dx.doi.org/10.1177/17562848231191670 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Argüelles-Arias, Federico
Valdés Delgado, Teresa
Maldonado Pérez, Belén
González Antuña, Jaime
Castro Laria, Luisa
Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title_full Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title_fullStr Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title_full_unstemmed Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title_short Intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
title_sort intravenous ustekinumab maintenance treatment in patients with loss of response to subcutaneous dosing
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467174/
https://www.ncbi.nlm.nih.gov/pubmed/37655058
http://dx.doi.org/10.1177/17562848231191670
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