Evidence map›Paper›PMID 41918827›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2026

Real-World Outcomes of Switching to Faricimab in Treatment-Experienced and Resistant Neovascular Age-Related Macular Degeneration: A Single-Centre Retrospective Study.

Christopher Stewart, Jaskaran Singh Bhangu, Parinita Keshav Swarnkar, Mohammed Rifat, Sarah Khalid, Ahmed Al-Janabi, Mahmoud H Awad, Gwyn Samuel Williams

Abstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Christopher StewartFaculty of Medicine, Health, and Life Science, Swansea University, Swansea, Wales, UK.ORCID 0009-0004-1111-3307
Jaskaran Singh BhanguOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.
Parinita Keshav SwarnkarOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.ORCID 0000-0002-3982-3173
Mohammed RifatOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.
Sarah KhalidOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.
Ahmed Al-JanabiOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.
Mahmoud H AwadOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.ORCID 0009-0001-9878-2447
Gwyn Samuel WilliamsOphthalmology Department, Singleton Hospital, Swansea Bay University Health Board, Swansea, Wales, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To evaluate anatomical, functional, and treatment burden outcomes of Faricimab in neovascular age-related macular degeneration (nAMD) patients with persistent disease activity despite prior anti-VEGF therapy. Patients and Methods: Single-centre retrospective study of 67 eyes switched to Faricimab (November 2022-December 2024). This cohort was unable to be extended beyond 4-6-week intervals on existing anti-VEGF therapy. All patients received three monthly loading doses followed by treat-and-extend regimen. Primary outcomes: central macular thickness (CMT), best-corrected visual acuity (BCVA), macular dryness over eight injections, and treatment interval extension. Results: The cohort had received mean 33 (range 10-78) prior anti-VEGF. Baseline mean BCVA was 0.42 logMAR (SD ± 0.28) and mean CMT was 244.5 μm (SD ± 62.2). Statistically significant CMT reduction occurred by injection 8 (-16.9 μm, p=0.0084). Complete macular dryness peaked by the time of third injection (43.3%) then declined to 32.8% at injection 8 (p=0.0089). Visual acuity remained unchanged (p=0.6043) with no correlation to CMT change (p=0.172). Treatment interval extension was achieved in 46.3% of patients (p=0.002). Dryness at injection 3 after switching to Faricimab did not predict treatment extension (p=0.217). Two patients (0.36% of total injections, 2/548) developed sterile intraocular inflammation requiring discontinuation. Conclusion: Faricimab switching achieves statistically significant but modest anatomical improvement in heavily pretreated nAMD with meaningful treatment burden reduction in 46.3% of eyes. Our analysis revealed treatment burden did not indicate the potential for treatment interval extension.

Indexed as

anti-VEGF switchingFaricimabtreat-and-extendtreatment-resistant nAMD

Identifiers

PMID41918827
PMCPMC13034787

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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.