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Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes
PURPOSE: To report the safety and effectiveness of intravitreal aflibercept (IVT-AFL) for diabetic macular edema (DME) in the real-world clinical practice setting in Japan. METHODS: In this prospective, multicenter, observational, post-marketing surveillance, patients with DME newly receiving IVT-AF...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581854/ https://www.ncbi.nlm.nih.gov/pubmed/35652946 http://dx.doi.org/10.1007/s00417-022-05703-9 |
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author | Sugimoto, Masahiko Handa, Chiharu Hirano, Kazufumi Sunaya, Toshiyuki Kondo, Mineo |
author_facet | Sugimoto, Masahiko Handa, Chiharu Hirano, Kazufumi Sunaya, Toshiyuki Kondo, Mineo |
author_sort | Sugimoto, Masahiko |
collection | PubMed |
description | PURPOSE: To report the safety and effectiveness of intravitreal aflibercept (IVT-AFL) for diabetic macular edema (DME) in the real-world clinical practice setting in Japan. METHODS: In this prospective, multicenter, observational, post-marketing surveillance, patients with DME newly receiving IVT-AFL were enrolled. During a 24-month follow-up, the primary outcome was the occurrence of safety events. Other pre-specified endpoints were effectiveness indicators, such as best-corrected visual acuity (BCVA), central retinal thickness, and injection frequency. RESULTS: In total, 646 patients administered at least one IVT-AFL injection were included in the safety analysis. During the follow-up period, adverse events occurred in 42 patients (6.50%), whereas adverse drug reactions occurred in 12 (1.86%). In the 12 patients who had adverse drug reactions, seven events occurred in seven patients within the first month of the most recent injection. In addition, 622 patients were included in the effectiveness analysis set. The number of injections over 24 months was 3.6 ± 3.0 (mean ± standard deviation [SD]). BCVA (logarithm of the minimum angle of resolution) was 0.437 ± 0.362 (mean ± SD) (n = 622) at baseline and 0.321 ± 0.348 (n = 177) after 24 months of treatment with IVT-AFL. Central retinal thickness was 440.8 ± 134.2 μm (mean ± SD) (n = 444) at baseline and 355.5 ± 126.4 μm (n = 140) at 24 months. CONCLUSION: Routine administration of IVT-AFL for DME was not associated with new safety concerns, and BCVA outcomes were maintained over 24 months in the real-world setting. Nonetheless, patients in this real-world setting received fewer injections than those in clinical trials, suggesting that a margin for improvement exists in clinical practice. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02425501. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00417-022-05703-9. |
format | Online Article Text |
id | pubmed-9581854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-95818542022-10-21 Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes Sugimoto, Masahiko Handa, Chiharu Hirano, Kazufumi Sunaya, Toshiyuki Kondo, Mineo Graefes Arch Clin Exp Ophthalmol Retinal Disorders PURPOSE: To report the safety and effectiveness of intravitreal aflibercept (IVT-AFL) for diabetic macular edema (DME) in the real-world clinical practice setting in Japan. METHODS: In this prospective, multicenter, observational, post-marketing surveillance, patients with DME newly receiving IVT-AFL were enrolled. During a 24-month follow-up, the primary outcome was the occurrence of safety events. Other pre-specified endpoints were effectiveness indicators, such as best-corrected visual acuity (BCVA), central retinal thickness, and injection frequency. RESULTS: In total, 646 patients administered at least one IVT-AFL injection were included in the safety analysis. During the follow-up period, adverse events occurred in 42 patients (6.50%), whereas adverse drug reactions occurred in 12 (1.86%). In the 12 patients who had adverse drug reactions, seven events occurred in seven patients within the first month of the most recent injection. In addition, 622 patients were included in the effectiveness analysis set. The number of injections over 24 months was 3.6 ± 3.0 (mean ± standard deviation [SD]). BCVA (logarithm of the minimum angle of resolution) was 0.437 ± 0.362 (mean ± SD) (n = 622) at baseline and 0.321 ± 0.348 (n = 177) after 24 months of treatment with IVT-AFL. Central retinal thickness was 440.8 ± 134.2 μm (mean ± SD) (n = 444) at baseline and 355.5 ± 126.4 μm (n = 140) at 24 months. CONCLUSION: Routine administration of IVT-AFL for DME was not associated with new safety concerns, and BCVA outcomes were maintained over 24 months in the real-world setting. Nonetheless, patients in this real-world setting received fewer injections than those in clinical trials, suggesting that a margin for improvement exists in clinical practice. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02425501. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00417-022-05703-9. Springer Berlin Heidelberg 2022-06-02 2022 /pmc/articles/PMC9581854/ /pubmed/35652946 http://dx.doi.org/10.1007/s00417-022-05703-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Retinal Disorders Sugimoto, Masahiko Handa, Chiharu Hirano, Kazufumi Sunaya, Toshiyuki Kondo, Mineo Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title | Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title_full | Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title_fullStr | Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title_full_unstemmed | Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title_short | Intravitreal aflibercept for diabetic macular edema in real-world clinical practice in Japan: 24-month outcomes |
title_sort | intravitreal aflibercept for diabetic macular edema in real-world clinical practice in japan: 24-month outcomes |
topic | Retinal Disorders |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581854/ https://www.ncbi.nlm.nih.gov/pubmed/35652946 http://dx.doi.org/10.1007/s00417-022-05703-9 |
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