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Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration
PURPOSE: To evaluate the short-term effects of intravitreal faricimab (IVF) in treatment-resistant neovascular age-related macular degeneration (nAMD) subjects previously treated with intravitreal aflibercept (IVA). METHODS: A retrospective review was conducted on nAMD patients undergoing IVA therap...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747838/ https://www.ncbi.nlm.nih.gov/pubmed/36532820 http://dx.doi.org/10.2147/OPTH.S395279 |
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author | Rush, Ryan B Rush, Sloan W |
author_facet | Rush, Ryan B Rush, Sloan W |
author_sort | Rush, Ryan B |
collection | PubMed |
description | PURPOSE: To evaluate the short-term effects of intravitreal faricimab (IVF) in treatment-resistant neovascular age-related macular degeneration (nAMD) subjects previously treated with intravitreal aflibercept (IVA). METHODS: A retrospective review was conducted on nAMD patients undergoing IVA therapy at a single private practice institution. Subjects were divided into Study and Control groups. Both Study and Control subjects had undergone ≥6 IVA treatments during the previous 12 months, ≥4 IVA treatments during the previous 6 months, had a central macular thickness (CMT) on optical coherence tomography (OCT) of ≥300 microns, and had observable intraretinal and/or subretinal fluid on OCT prior to group assignment. Study subjects were switched from IVA to IVF and received 3 treatments within 4 months. Control subjects remained on IVA during the same time period and received 3 treatments within 4 months. RESULTS: There were a total of 55 subjects analyzed. There were 39.3% (11/28) in the Study Group and 7.4% (2/27) in the Control Group attaining a CMT of less than 300 microns without retinal fluid on OCT at the end of the 4-month study period (p = 0.004). There were 35.7% (10/28) in the Study Group and 7.4% (2/27) in the Control Group gaining 2 or more lines of visual acuity at the end of the 4-month study period (p = 0.008). CONCLUSION: IVF can improve the visual and anatomic outcomes in a significant minority of treatment-resistant nAMD subjects previously managed with IVA. A greater follow-up period is needed to determine if such improvements can be maintained. |
format | Online Article Text |
id | pubmed-9747838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-97478382022-12-15 Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration Rush, Ryan B Rush, Sloan W Clin Ophthalmol Original Research PURPOSE: To evaluate the short-term effects of intravitreal faricimab (IVF) in treatment-resistant neovascular age-related macular degeneration (nAMD) subjects previously treated with intravitreal aflibercept (IVA). METHODS: A retrospective review was conducted on nAMD patients undergoing IVA therapy at a single private practice institution. Subjects were divided into Study and Control groups. Both Study and Control subjects had undergone ≥6 IVA treatments during the previous 12 months, ≥4 IVA treatments during the previous 6 months, had a central macular thickness (CMT) on optical coherence tomography (OCT) of ≥300 microns, and had observable intraretinal and/or subretinal fluid on OCT prior to group assignment. Study subjects were switched from IVA to IVF and received 3 treatments within 4 months. Control subjects remained on IVA during the same time period and received 3 treatments within 4 months. RESULTS: There were a total of 55 subjects analyzed. There were 39.3% (11/28) in the Study Group and 7.4% (2/27) in the Control Group attaining a CMT of less than 300 microns without retinal fluid on OCT at the end of the 4-month study period (p = 0.004). There were 35.7% (10/28) in the Study Group and 7.4% (2/27) in the Control Group gaining 2 or more lines of visual acuity at the end of the 4-month study period (p = 0.008). CONCLUSION: IVF can improve the visual and anatomic outcomes in a significant minority of treatment-resistant nAMD subjects previously managed with IVA. A greater follow-up period is needed to determine if such improvements can be maintained. Dove 2022-12-09 /pmc/articles/PMC9747838/ /pubmed/36532820 http://dx.doi.org/10.2147/OPTH.S395279 Text en © 2022 Rush and Rush. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Rush, Ryan B Rush, Sloan W Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title | Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title_full | Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title_fullStr | Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title_full_unstemmed | Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title_short | Intravitreal Faricimab for Aflibercept-Resistant Neovascular Age-Related Macular Degeneration |
title_sort | intravitreal faricimab for aflibercept-resistant neovascular age-related macular degeneration |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747838/ https://www.ncbi.nlm.nih.gov/pubmed/36532820 http://dx.doi.org/10.2147/OPTH.S395279 |
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