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Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER

INTRODUCTION: The HAWK and HARRIER studies evaluated the efficacy and safety of brolucizumab versus aflibercept in treatment-naïve eyes with neovascular age-related macular degeneration. Based on the study design, brolucizumab-treated eyes adjusted to a q8w regimen because the presence of disease ac...

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Autores principales: Tadayoni, Ramin, Jaffe, Glenn J., Holz, Frank G., Schmidt-Erfurth, Ursula, Takahashi, Kanji, Cheung, Chui Ming Gemmy, Hariprasad, Seenu M., Gedif, Kinfemichael, Olsen, Rasmus, Best, Catherine, Igwe, Franklin, Kaiser, Peter K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287590/
https://www.ncbi.nlm.nih.gov/pubmed/37294524
http://dx.doi.org/10.1007/s40123-023-00735-8
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author Tadayoni, Ramin
Jaffe, Glenn J.
Holz, Frank G.
Schmidt-Erfurth, Ursula
Takahashi, Kanji
Cheung, Chui Ming Gemmy
Hariprasad, Seenu M.
Gedif, Kinfemichael
Olsen, Rasmus
Best, Catherine
Igwe, Franklin
Kaiser, Peter K.
author_facet Tadayoni, Ramin
Jaffe, Glenn J.
Holz, Frank G.
Schmidt-Erfurth, Ursula
Takahashi, Kanji
Cheung, Chui Ming Gemmy
Hariprasad, Seenu M.
Gedif, Kinfemichael
Olsen, Rasmus
Best, Catherine
Igwe, Franklin
Kaiser, Peter K.
author_sort Tadayoni, Ramin
collection PubMed
description INTRODUCTION: The HAWK and HARRIER studies evaluated the efficacy and safety of brolucizumab versus aflibercept in treatment-naïve eyes with neovascular age-related macular degeneration. Based on the study design, brolucizumab-treated eyes adjusted to a q8w regimen because the presence of disease activity (DA) at the end of the matched loading phase (Week 16) could not subsequently extend to a q12w interval. The aim of this post hoc analysis was to assess subsequent DA in this subgroup to determine the potential for interval extensions during the first year of treatment. METHODS: Pooled data from the brolucizumab 6 mg arms and aflibercept arms of HAWK and HARRIER were included. Presence of DA was determined by the masked investigator based on their assessment of functional and anatomical parameters measured by optical coherence tomography. DA was compared at DA assessments, conducted at Weeks 16, 20, 32, and 44; fluid was also assessed at the primary analysis at Week 48. RESULTS: Fewer brolucizumab- (22.8%) than aflibercept-treated (32.2%) eyes had DA at the first DA assessment at Week 16. In eyes with investigator-identified DA at Week 16, BCVA change from baseline to Week 96 was comparable between treatment arms. Fewer brolucizumab- than aflibercept-treated eyes had DA at each subsequent DA assessment in Year 1: 31.8% vs 39.1% (Week 20), 27.3% vs 43.5% (Week 32), and 17.3% vs 31.2% (Week 44). Fewer eyes treated with brolucizumab than aflibercept had intraretinal and/or subretinal fluid: 35.3% vs 43.5% (Week 20), 55.8% vs 69.6% (Week 32), 30.0% vs 43.1% (Week 44), and 48.6% vs 68.6% (Week 48). CONCLUSION: These findings indicate that, in eyes that still had DA 8 weeks after the final dose of loading phase, brolucizumab-treated eyes had improved fluid resolution and higher potential for treatment interval extension than aflibercept-treated eyes during the first year of treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40123-023-00735-8.
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spelling pubmed-102875902023-06-24 Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER Tadayoni, Ramin Jaffe, Glenn J. Holz, Frank G. Schmidt-Erfurth, Ursula Takahashi, Kanji Cheung, Chui Ming Gemmy Hariprasad, Seenu M. Gedif, Kinfemichael Olsen, Rasmus Best, Catherine Igwe, Franklin Kaiser, Peter K. Ophthalmol Ther Brief Report INTRODUCTION: The HAWK and HARRIER studies evaluated the efficacy and safety of brolucizumab versus aflibercept in treatment-naïve eyes with neovascular age-related macular degeneration. Based on the study design, brolucizumab-treated eyes adjusted to a q8w regimen because the presence of disease activity (DA) at the end of the matched loading phase (Week 16) could not subsequently extend to a q12w interval. The aim of this post hoc analysis was to assess subsequent DA in this subgroup to determine the potential for interval extensions during the first year of treatment. METHODS: Pooled data from the brolucizumab 6 mg arms and aflibercept arms of HAWK and HARRIER were included. Presence of DA was determined by the masked investigator based on their assessment of functional and anatomical parameters measured by optical coherence tomography. DA was compared at DA assessments, conducted at Weeks 16, 20, 32, and 44; fluid was also assessed at the primary analysis at Week 48. RESULTS: Fewer brolucizumab- (22.8%) than aflibercept-treated (32.2%) eyes had DA at the first DA assessment at Week 16. In eyes with investigator-identified DA at Week 16, BCVA change from baseline to Week 96 was comparable between treatment arms. Fewer brolucizumab- than aflibercept-treated eyes had DA at each subsequent DA assessment in Year 1: 31.8% vs 39.1% (Week 20), 27.3% vs 43.5% (Week 32), and 17.3% vs 31.2% (Week 44). Fewer eyes treated with brolucizumab than aflibercept had intraretinal and/or subretinal fluid: 35.3% vs 43.5% (Week 20), 55.8% vs 69.6% (Week 32), 30.0% vs 43.1% (Week 44), and 48.6% vs 68.6% (Week 48). CONCLUSION: These findings indicate that, in eyes that still had DA 8 weeks after the final dose of loading phase, brolucizumab-treated eyes had improved fluid resolution and higher potential for treatment interval extension than aflibercept-treated eyes during the first year of treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40123-023-00735-8. Springer Healthcare 2023-06-09 2023-08 /pmc/articles/PMC10287590/ /pubmed/37294524 http://dx.doi.org/10.1007/s40123-023-00735-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Brief Report
Tadayoni, Ramin
Jaffe, Glenn J.
Holz, Frank G.
Schmidt-Erfurth, Ursula
Takahashi, Kanji
Cheung, Chui Ming Gemmy
Hariprasad, Seenu M.
Gedif, Kinfemichael
Olsen, Rasmus
Best, Catherine
Igwe, Franklin
Kaiser, Peter K.
Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title_full Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title_fullStr Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title_full_unstemmed Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title_short Potential for Treatment Interval Extension in Eyes with nAMD Disease Activity Post Loading Phase in HAWK and HARRIER
title_sort potential for treatment interval extension in eyes with namd disease activity post loading phase in hawk and harrier
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287590/
https://www.ncbi.nlm.nih.gov/pubmed/37294524
http://dx.doi.org/10.1007/s40123-023-00735-8
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