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Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience

Objective. To evaluate, in three Spanish tertiary referral centres, the short-term safety and efficacy of golimumab (GLM) for treatment of immune-mediated uveitis resistant to previous immunosuppressive therapy. Methods. Nonrandomized retrospective interventional case series. Thirteen patients with...

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Autores principales: Cordero-Coma, Miguel, Calvo-Río, Vanesa, Adán, Alfredo, Blanco, Ricardo, Álvarez-Castro, Carolina, Mesquida, Marina, Calleja, Sara, González-Gay, Miguel A., Ruíz de Morales, José G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058145/
https://www.ncbi.nlm.nih.gov/pubmed/24976689
http://dx.doi.org/10.1155/2014/717598
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author Cordero-Coma, Miguel
Calvo-Río, Vanesa
Adán, Alfredo
Blanco, Ricardo
Álvarez-Castro, Carolina
Mesquida, Marina
Calleja, Sara
González-Gay, Miguel A.
Ruíz de Morales, José G.
author_facet Cordero-Coma, Miguel
Calvo-Río, Vanesa
Adán, Alfredo
Blanco, Ricardo
Álvarez-Castro, Carolina
Mesquida, Marina
Calleja, Sara
González-Gay, Miguel A.
Ruíz de Morales, José G.
author_sort Cordero-Coma, Miguel
collection PubMed
description Objective. To evaluate, in three Spanish tertiary referral centres, the short-term safety and efficacy of golimumab (GLM) for treatment of immune-mediated uveitis resistant to previous immunosuppressive therapy. Methods. Nonrandomized retrospective interventional case series. Thirteen patients with different types of uveitis that were resistant to treatment with at least 2 previous immunosuppressors were included in this study. All included patients were treated with GLM (50 mg every four weeks) during at least 6 months. Clinical evaluation and treatment-related side effects were assessed at least four times in all included patients. Results. Eight men and 5 women (22 affected eyes) with a median age of 30 years (range 20–38) and active immune-mediated uveitides were studied. GLM was used in combination with conventional immunosuppressors in 7 patients (53.8%). GLM therapy achieved complete control of inflammation in 12/13 patients (92.3%) after six months of treatment. There was a statistically significant improvement in mean BCVA (0.60 versus 0.68, P = 0.009) and mean 1 mm central retinal thickness (317 versus 261.2 μ, P = 0.05) at the six-month endpoint when compared to basal values. No major systemic adverse effects associated with GLM therapy were observed. Conclusions. GLM is a new and promising therapeutic option for patients with severe and refractory uveitis.
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spelling pubmed-40581452014-06-29 Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience Cordero-Coma, Miguel Calvo-Río, Vanesa Adán, Alfredo Blanco, Ricardo Álvarez-Castro, Carolina Mesquida, Marina Calleja, Sara González-Gay, Miguel A. Ruíz de Morales, José G. Mediators Inflamm Clinical Study Objective. To evaluate, in three Spanish tertiary referral centres, the short-term safety and efficacy of golimumab (GLM) for treatment of immune-mediated uveitis resistant to previous immunosuppressive therapy. Methods. Nonrandomized retrospective interventional case series. Thirteen patients with different types of uveitis that were resistant to treatment with at least 2 previous immunosuppressors were included in this study. All included patients were treated with GLM (50 mg every four weeks) during at least 6 months. Clinical evaluation and treatment-related side effects were assessed at least four times in all included patients. Results. Eight men and 5 women (22 affected eyes) with a median age of 30 years (range 20–38) and active immune-mediated uveitides were studied. GLM was used in combination with conventional immunosuppressors in 7 patients (53.8%). GLM therapy achieved complete control of inflammation in 12/13 patients (92.3%) after six months of treatment. There was a statistically significant improvement in mean BCVA (0.60 versus 0.68, P = 0.009) and mean 1 mm central retinal thickness (317 versus 261.2 μ, P = 0.05) at the six-month endpoint when compared to basal values. No major systemic adverse effects associated with GLM therapy were observed. Conclusions. GLM is a new and promising therapeutic option for patients with severe and refractory uveitis. Hindawi Publishing Corporation 2014 2014-05-28 /pmc/articles/PMC4058145/ /pubmed/24976689 http://dx.doi.org/10.1155/2014/717598 Text en Copyright © 2014 Miguel Cordero-Coma et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Cordero-Coma, Miguel
Calvo-Río, Vanesa
Adán, Alfredo
Blanco, Ricardo
Álvarez-Castro, Carolina
Mesquida, Marina
Calleja, Sara
González-Gay, Miguel A.
Ruíz de Morales, José G.
Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title_full Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title_fullStr Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title_full_unstemmed Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title_short Golimumab as Rescue Therapy for Refractory Immune-Mediated Uveitis: A Three-Center Experience
title_sort golimumab as rescue therapy for refractory immune-mediated uveitis: a three-center experience
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058145/
https://www.ncbi.nlm.nih.gov/pubmed/24976689
http://dx.doi.org/10.1155/2014/717598
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