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Journal article

Real-World Data on Faricimab Switching in Treatment-Refractory Neovascular Age-Related Macular Degeneration

Abstract:
Faricimab is a newly approved bispecific antibody for neovascular age-related macular degeneration (nAMD). Our study aims to evaluate clinical outcomes of faricimab switching in patients with treatment-refractory nAMD; determine parameters that predict these outcomes; and obtain patient subjective experience on this new injection. This is a retrospective case review with clinical and imaging data from a tertiary referral unit (Birmingham and Midland Eye Centre, UK), involving patients who were switched to faricimab between 1 January and 1 December 2023. In all, 63 eyes (54 patients) with a mean age of 79.2 ± 7.8 and mean of 41.5 ± 22.4 previous anti-VEGF injections were analysed. With a mean of 4.81 ± 1.16 faricimab injections over 6.98 ± 1.75 months, post-treatment visual acuity was logMAR 0.49 ± 0.36 and central macular thickness (CMT) was 320.3 ± 97.9 µm. After first dose, 39.1% achieved complete dryness and 89.1% had anatomical improvement. Presence of subretinal fluid was a predictor of better functional outcomes (p = 0.001, β = -0.182), while initial CMT predicted better anatomical outcomes (p = 0.001, β = 0.688). Compared to their experiences of previous anti-VEGF injections, 89% of patients reported no more discomfort and 87.0% experienced no more floaters, photopsia, or bubbles post-injection. Faricimab switching has anatomical efficacy but limited functional improvement in treatment-refractory AMD. Patient experiences of faricimab compared to previous injections were overall positive.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3390/life14020193

Authors


More by this author
Institution:
University of Oxford
Oxford college:
Christ Church
Role:
Author
ORCID:
0000-0003-4296-2948
More by this author
Role:
Author
ORCID:
0000-0002-8571-2503


Publisher:
MDPI
Journal:
Life More from this journal
Volume:
14
Issue:
2
Pages:
193
Publication date:
2024-01-29
DOI:
ISSN:
2075-1729
Pmid:
38398702


Language:
English
Keywords:
Source identifiers:
1800702
Deposit date:
2024-05-30
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