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Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration

PURPOSE: Intravitreal injection of anti-VEGF drugs has become standard therapy for patients with exudative age-related macular degeneration (AMD). However, some patients do not exhibit sufficient response to the drugs for suppression of choroidal neovascularization activity. We investigated the effi...

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Autores principales: Koike, Naoko, Otsuji, Tsuyoshi, Tsumura, Akiko, Miki, Katsuaki, Sakai, Yukio, Nishimura, Tetsuya, Takahashi, Kanji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643053/
https://www.ncbi.nlm.nih.gov/pubmed/31409963
http://dx.doi.org/10.2147/OPTH.S206910
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author Koike, Naoko
Otsuji, Tsuyoshi
Tsumura, Akiko
Miki, Katsuaki
Sakai, Yukio
Nishimura, Tetsuya
Takahashi, Kanji
author_facet Koike, Naoko
Otsuji, Tsuyoshi
Tsumura, Akiko
Miki, Katsuaki
Sakai, Yukio
Nishimura, Tetsuya
Takahashi, Kanji
author_sort Koike, Naoko
collection PubMed
description PURPOSE: Intravitreal injection of anti-VEGF drugs has become standard therapy for patients with exudative age-related macular degeneration (AMD). However, some patients do not exhibit sufficient response to the drugs for suppression of choroidal neovascularization activity. We investigated the efficacy of switchback from ranibizumab to aflibercept in patients with AMD who could not achieve further benefit beyond initial therapy of aflibercept injection. METHODS: Eleven eyes of eleven patients were included in this study. Two patients were nonresponders, and nine exhibited tachyphylaxis to aflibercept. All patients received three monthly injections of ranibizumab as an initial phase of switching and received aflibercept as a switchback drug. We investigated changes in injection interval, visual acuity, and central retinal thickness. RESULTS: In four patients (36.4%), injection interval was extended. The interval was 6.73 weeks before switch and 9.27 weeks after switchback (P=0.96). LogMAR visual acuity was 0.22 before switch and 0.24 after switchback (P=0.62). Central retinal thickness was 306.8 µm before switch and 256.1 after switchback (P=0.13). In all patients who were nonresponders to aflibercept, injection interval could not be extended. CONCLUSION: A switchback from ranibizumab to aflibercept may be beneficial in some patients with AMD who exhibit tachyphylaxis to aflibercept.
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spelling pubmed-66430532019-08-13 Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration Koike, Naoko Otsuji, Tsuyoshi Tsumura, Akiko Miki, Katsuaki Sakai, Yukio Nishimura, Tetsuya Takahashi, Kanji Clin Ophthalmol Original Research PURPOSE: Intravitreal injection of anti-VEGF drugs has become standard therapy for patients with exudative age-related macular degeneration (AMD). However, some patients do not exhibit sufficient response to the drugs for suppression of choroidal neovascularization activity. We investigated the efficacy of switchback from ranibizumab to aflibercept in patients with AMD who could not achieve further benefit beyond initial therapy of aflibercept injection. METHODS: Eleven eyes of eleven patients were included in this study. Two patients were nonresponders, and nine exhibited tachyphylaxis to aflibercept. All patients received three monthly injections of ranibizumab as an initial phase of switching and received aflibercept as a switchback drug. We investigated changes in injection interval, visual acuity, and central retinal thickness. RESULTS: In four patients (36.4%), injection interval was extended. The interval was 6.73 weeks before switch and 9.27 weeks after switchback (P=0.96). LogMAR visual acuity was 0.22 before switch and 0.24 after switchback (P=0.62). Central retinal thickness was 306.8 µm before switch and 256.1 after switchback (P=0.13). In all patients who were nonresponders to aflibercept, injection interval could not be extended. CONCLUSION: A switchback from ranibizumab to aflibercept may be beneficial in some patients with AMD who exhibit tachyphylaxis to aflibercept. Dove 2019-07-15 /pmc/articles/PMC6643053/ /pubmed/31409963 http://dx.doi.org/10.2147/OPTH.S206910 Text en © 2019 Koike et al. http://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/). 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
Koike, Naoko
Otsuji, Tsuyoshi
Tsumura, Akiko
Miki, Katsuaki
Sakai, Yukio
Nishimura, Tetsuya
Takahashi, Kanji
Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title_full Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title_fullStr Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title_full_unstemmed Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title_short Results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
title_sort results of switchback from ranibizumab to aflibercept in patients with exudative age-related macular degeneration
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643053/
https://www.ncbi.nlm.nih.gov/pubmed/31409963
http://dx.doi.org/10.2147/OPTH.S206910
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