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Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review
BACKGROUND: Uveitis is a group of intraocular inflammatory diseases whose primary treatment involves immunosuppression. Although corticosteroids (CSs) remain the mainstay therapy, sirolimus is among the recently studied immunomodulatory drugs for treating noninfectious uveitis (NIU). OBJECTIVE: The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478489/ https://www.ncbi.nlm.nih.gov/pubmed/31114144 http://dx.doi.org/10.2147/OPTH.S198401 |
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author | Cabahug, Vicente Lorenzo O Uy, Harvey S Yu-Keh, Ellen Sapno, Kristine Joy D |
author_facet | Cabahug, Vicente Lorenzo O Uy, Harvey S Yu-Keh, Ellen Sapno, Kristine Joy D |
author_sort | Cabahug, Vicente Lorenzo O |
collection | PubMed |
description | BACKGROUND: Uveitis is a group of intraocular inflammatory diseases whose primary treatment involves immunosuppression. Although corticosteroids (CSs) remain the mainstay therapy, sirolimus is among the recently studied immunomodulatory drugs for treating noninfectious uveitis (NIU). OBJECTIVE: The aim of this review was to assess and summarize the updated evidence on the outcomes of treatment with sirolimus for NIU. MATERIALS AND METHODS: Two reviewers conducted a systematic search on November 5, 2018, of electronic databases (EMBASE, MEDLINE, and The Cochrane Library) and clinical trial registers having no restrictions on language or publication date. The primary outcome was uveitis activity as measured by vitreous haze (VH), while the secondary outcomes included central macular thickness (CMT), best-corrected visual acuity (BCVA), CS-sparing effect, IOP elevation, and other adverse events. A meta-analysis was conducted on selected studies with appropriate clinical and methodological homogeneity. RESULTS: Seven studies were included and reviewed. Four randomized clinical trials were eligible for meta-analysis: SAVE 2013, One-year outcomes of the SAVE study, SAVE 2 2016, SAKURA 2016. The pooled proportions of inflammation control (VH improvement) were 38% (95% CI 16.19%–62.66%) during a 6-month follow-up and 49.97% (95% CI 16.19%–83.03%) during a 6- to 12-month follow-up with the latter showing a significantly higher response rate (p=0.0472). BCVA improvement was 62.2% (95% CI 33.17%–87.11%) during a 6-month follow-up and 56.86% (95% CI 20.91%–89.05%) during a 6- to 12-month follow-up with no significant difference between the two (p=0.3705). Increased IOP remained at 7.11% (95% CI 3.46%–12.68%) for both a 6-month follow-up and up to a 12-month follow-up duration. The CS-sparing effect of sirolimus was also well demonstrated. A reduction in CMT was observed, and only minor drug-related adverse events were reported in all the studies reviewed. CONCLUSION: This review provided evidence that sirolimus is a promising treatment option for controlling inflammatory activity, improving visual acuity, and sparing CS use with minor adverse events for NIU. |
format | Online Article Text |
id | pubmed-6478489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64784892019-05-21 Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review Cabahug, Vicente Lorenzo O Uy, Harvey S Yu-Keh, Ellen Sapno, Kristine Joy D Clin Ophthalmol Review BACKGROUND: Uveitis is a group of intraocular inflammatory diseases whose primary treatment involves immunosuppression. Although corticosteroids (CSs) remain the mainstay therapy, sirolimus is among the recently studied immunomodulatory drugs for treating noninfectious uveitis (NIU). OBJECTIVE: The aim of this review was to assess and summarize the updated evidence on the outcomes of treatment with sirolimus for NIU. MATERIALS AND METHODS: Two reviewers conducted a systematic search on November 5, 2018, of electronic databases (EMBASE, MEDLINE, and The Cochrane Library) and clinical trial registers having no restrictions on language or publication date. The primary outcome was uveitis activity as measured by vitreous haze (VH), while the secondary outcomes included central macular thickness (CMT), best-corrected visual acuity (BCVA), CS-sparing effect, IOP elevation, and other adverse events. A meta-analysis was conducted on selected studies with appropriate clinical and methodological homogeneity. RESULTS: Seven studies were included and reviewed. Four randomized clinical trials were eligible for meta-analysis: SAVE 2013, One-year outcomes of the SAVE study, SAVE 2 2016, SAKURA 2016. The pooled proportions of inflammation control (VH improvement) were 38% (95% CI 16.19%–62.66%) during a 6-month follow-up and 49.97% (95% CI 16.19%–83.03%) during a 6- to 12-month follow-up with the latter showing a significantly higher response rate (p=0.0472). BCVA improvement was 62.2% (95% CI 33.17%–87.11%) during a 6-month follow-up and 56.86% (95% CI 20.91%–89.05%) during a 6- to 12-month follow-up with no significant difference between the two (p=0.3705). Increased IOP remained at 7.11% (95% CI 3.46%–12.68%) for both a 6-month follow-up and up to a 12-month follow-up duration. The CS-sparing effect of sirolimus was also well demonstrated. A reduction in CMT was observed, and only minor drug-related adverse events were reported in all the studies reviewed. CONCLUSION: This review provided evidence that sirolimus is a promising treatment option for controlling inflammatory activity, improving visual acuity, and sparing CS use with minor adverse events for NIU. Dove Medical Press 2019-04-18 /pmc/articles/PMC6478489/ /pubmed/31114144 http://dx.doi.org/10.2147/OPTH.S198401 Text en © 2019 Cabahug et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Cabahug, Vicente Lorenzo O Uy, Harvey S Yu-Keh, Ellen Sapno, Kristine Joy D Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title | Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title_full | Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title_fullStr | Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title_full_unstemmed | Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title_short | Outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
title_sort | outcomes of treatment with sirolimus for non-infectious uveitis: a meta-analysis and systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478489/ https://www.ncbi.nlm.nih.gov/pubmed/31114144 http://dx.doi.org/10.2147/OPTH.S198401 |
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