Evidence map›Paper›PMID 42642671›Full record

ArticleInternational ophthalmology2026

Early anatomical rescue after switching to aflibercept 8 mg in faricimab-refractory neovascular AMD.

Woohyok Chang

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Article in International ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

1 author.

Woohyok ChangChang's Retina Center, Daegu, South Korea. woohchang@gmail.com.ORCID https://orcid.org/0009-0000-7505-4079

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate early anatomical outcomes after switching to aflibercept 8 mg in eyes with neovascular age-related macular degeneration (nAMD) refractory to faricimab.

methodsThis retrospective study included 32 eyes of 31 patients with nAMD who were switched from faricimab to aflibercept 8 mg due to persistent or recurrent fluid. Main outcome measures included central subfield thickness (CST), best-corrected visual acuity (BCVA), and proportion of eyes achieving fluid-free macula at weeks 8 and 16. Subgroup analyses were performed based on diagnosis (PCV vs non-PCV) and prior treatment history.

resultsMean CST decreased significantly from 374.0 ± 88.3 μm at the time of switch to 324.6 ± 80.6 μm at week 8 (p = 0.003) and 321.4 ± 84.0 μm at week 16 (p = 0.002). Fluid-free rate increased from 18.8 to 43.8% at week 8 and 46.9% at week 16. Mean BCVA remained stable throughout. Both PCV (n=12) and non-PCV (n=20) subgroups showed significant CST reduction. Eyes treatment-naïve before faricimab and those treatment-experienced before faricimab demonstrated comparable responses. No serious adverse events were observed.

conclusionsSwitching to aflibercept 8 mg resulted in rapid and significant anatomical improvement in faricimab-refractory nAMD, with most improvement occurring by week 8. The treatment was effective across diagnostic subtypes including PCV and regardless of prior treatment burden. Although early anatomical improvement was observed, the long-term durability of this response remains unknown and warrants further study.

Indexed as

Drug SubstitutionMacula LuteaReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVisual AcuityWet Macular DegenerationAgedAged, 80 and overAngiogenesis InhibitorsAntibodies, BispecificDose-Response Relationship, DrugFemaleFluorescein AngiographyFollow-Up StudiesFundus OculiHumansafliberceptAngiogenesis InhibitorsAntibodies, BispecificfaricimabReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsAflibercept 8 mgFaricimabNeovascular age-related macular degenerationPolypoidal choroidal vasculopathyRefractorySwitch therapy

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.