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Efficacy of intravitreal faricimab therapy for polypoidal choroidal vasculopathy: A systematic review and meta‐analysis

dc.contributor.authorArnold‐Vangsted, Andreas
dc.contributor.authorSchou, Marianne G.
dc.contributor.authorBalaratnasingam, Chandrakumar
dc.contributor.authorCehofski, Lasse J.
dc.contributor.authorChhablani, Jay
dc.contributor.authorvan Dijk, Elon H. C.
dc.contributor.authorEriksen, Nathalie S.
dc.contributor.authorGrauslund, Jakob
dc.contributor.authorHajari, Javad N.
dc.contributor.authorSabaner, M. Cem
dc.contributor.authorSchneider, Miklos
dc.contributor.authorSubhi, Yousif
dc.date.accessioned2026-01-04T21:05:41Z
dc.date.issued2024-11-16
dc.description.abstractAbstractPolypoidal choroidal vasculopathy (PCV) is an aneurismal type of macular neovascularization that show similarities with age‐related macular degeneration and diseases that are part of the pachychoroid disease spectrum. Exudative changes in PCV can be treated with intravitreal anti‐vascular endothelial growth factor monotherapy; however, a combination therapy with photodynamic therapy may be required. In this systematic review and meta‐analysis, we evaluated the efficacy of faricimab for PCV. We searched 12 literature databases for eligible studies. All study evaluation and data extraction were made by two authors in duplicate. Studies eligible for analysis were included for a qualitative and quantitative review. We identified seven studies with data from 150 eyes with PCV, five studies were of treatment‐naïve eyes who were commenced in faricimab monotherapy, and two studies were of switch‐over to faricimab from other anti‐VEGF drugs. After faricimab loading dose in treatment‐naïve eyes, the best‐corrected visual acuity (BCVA) remained stable at −0.09 (95% CI: −0.20–0.03) logMAR, central retinal thickness (CRT) decreased −169 (95% CI: −311–−27) μm, and 48.7 (95% CI: 32.5–65.0) % of eyes obtained polyp closure. In switch‐over eyes, 57%–67% experienced fluid reduction and 21% were able to extend their treatment interval. In conclusion, faricimab monotherapy for PCV leads to acceptable clinical outcomes in terms of stable BCVA, reduction of CRT, and high incidence of polyp closure. Some cases may benefit from a switch to faricimab. However, long‐term efficacy studies and controlled comparative studies are warranted.
dc.description.urihttps://doi.org/10.1111/aos.16797
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/39548881
dc.description.urihttps://vbn.aau.dk/da/publications/4aca65aa-3f55-4860-a671-0dfa490ba071
dc.description.urihttp://www.scopus.com/inward/record.url?scp=105002490878&partnerID=8YFLogxK
dc.description.urihttps://hdl.handle.net/1887/4196100
dc.description.urihttps://portal.findresearcher.sdu.dk/da/publications/6e378aa0-ab22-496e-a04b-b7cd4cbae7f7
dc.identifier.doi10.1111/aos.16797
dc.identifier.eissn1755-3768
dc.identifier.endpage256
dc.identifier.issn1755-375X
dc.identifier.openairedoi_dedup___::d1103a35a0b8521c5b6d5273cfd6c5ca
dc.identifier.orcid0009-0007-7193-7975
dc.identifier.orcid0000-0002-2150-7754
dc.identifier.orcid0000-0003-1772-3558
dc.identifier.orcid0000-0001-5019-0736
dc.identifier.orcid0000-0003-1488-4743
dc.identifier.orcid0000-0001-6620-5365
dc.identifier.pubmed39548881
dc.identifier.scopus2-s2.0-105002490878
dc.identifier.startpage247
dc.identifier.urihttps://hdl.handle.net/20.500.12597/42241
dc.identifier.volume103
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofActa Ophthalmologica
dc.rightsOPEN
dc.subjectFundus Oculi
dc.subjectefficacy
dc.subjectVisual Acuity
dc.subjectChoroidal Neovascularization/drug therapy
dc.subjectPolypoidal Choroidal Vasculopathy
dc.subjectfaricimab
dc.subjectpolypoidal choroidal vasculopathy
dc.subjectAntibodies
dc.subjectChoroid/blood supply
dc.subjectTreatment Outcome
dc.subjectPolyps/drug therapy
dc.subjectsystematic review
dc.subjectOptical Coherence
dc.subjectanti-VEGF
dc.subjectIntravitreal Injections
dc.subjectAngiogenesis Inhibitors/administration & dosage
dc.subjectHumans
dc.subjectVascular Endothelial Growth Factor A/antagonists & inhibitors
dc.subjectBispecific
dc.subjectFluorescein Angiography
dc.subjectTomography
dc.titleEfficacy of intravitreal faricimab therapy for polypoidal choroidal vasculopathy: A systematic review and meta‐analysis
dc.typeArticle
dspace.entity.typePublication
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Exudative changes in PCV can be treated with intravitreal anti‐vascular endothelial growth factor monotherapy; however, a combination therapy with photodynamic therapy may be required. In this systematic review and meta‐analysis, we evaluated the efficacy of faricimab for PCV. We searched 12 literature databases for eligible studies. All study evaluation and data extraction were made by two authors in duplicate. Studies eligible for analysis were included for a qualitative and quantitative review. We identified seven studies with data from 150 eyes with PCV, five studies were of treatment‐naïve eyes who were commenced in faricimab monotherapy, and two studies were of switch‐over to faricimab from other anti‐VEGF drugs. After faricimab loading dose in treatment‐naïve eyes, the best‐corrected visual acuity (BCVA) remained stable at −0.09 (95% CI: −0.20–0.03) logMAR, central retinal thickness (CRT) decreased −169 (95% CI: −311–−27) μm, and 48.7 (95% CI: 32.5–65.0) % of eyes obtained polyp closure. In switch‐over eyes, 57%–67% experienced fluid reduction and 21% were able to extend their treatment interval. In conclusion, faricimab monotherapy for PCV leads to acceptable clinical outcomes in terms of stable BCVA, reduction of CRT, and high incidence of polyp closure. Some cases may benefit from a switch to faricimab. 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