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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4058145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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