Evidence map›Paper›PMID 41524752›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2026

VEGF-inhibitor switch trial in poor-responsive neovascular age-related macular degeneration: assessing brolucizumab vs. faricimab: VISTA study.

Adnan Kilani, Denise Vogt, Vasiliki Moysidi, Abdelrahman Assaf, Armin Wolf, Efstathios Vounotrypidis

Abstract readComparative Study
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Adnan KilaniDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany. adnan.kilani@uniklinik-ulm.de.ORCID http://orcid.org/0000-0003-4134-091X
Denise VogtDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany.
Vasiliki MoysidiDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany.
Abdelrahman AssafDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany.ORCID http://orcid.org/0000-0002-9350-2645
Armin WolfDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany.ORCID http://orcid.org/0000-0002-6991-2214
Efstathios VounotrypidisDepartment of Ophthalmology, Ulm University Hospital, Ulm, Prittwitzstraße 43, 89075, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo compare short-term (12 weeks) and long-term (48 weeks) anatomical and functional outcomes after switching to brolucizumab (BRZ) or faricimab (FAR) under a treat-and-extend (TAE) regimen without an initial loading phase in eyes with poor-responsive neovascular age-related macular degeneration (nAMD).

methodsThis retrospective, single-center study included eyes with poor-responsive nAMD previously treated with anti-VEGF agents that were switched to BRZ or FAR between 2022 and 2025. Functional outcomes (best-corrected visual acuity [BCVA]) and anatomical parameters (central subfield thickness [CST], fibrovascular pigment epithelial detachment [fvPED] height, intraretinal/subretinal fluid [IRF/SRF], subretinal hyperreflective material [SHRM]) were assessed at baseline, week 12, and week 48. Injection frequency, interval extension, and safety were recorded.

resultsSixty-six eyes (41 BRZ, 25 FAR) were included. At 12 weeks, BCVA remained stable (BRZ 0.49 logMAR, FAR 0.40; p = 0.10). CST decreased significantly in both groups, greater with BRZ (243 μm vs. 280 μm; p = 0.04). Mean injections (2.95 vs. 3.2; p = 0.12) and intervals (5.9 vs. 5.6 weeks; p = 0.90) were comparable; no intraocular inflammation (IOI) occurred. At 48 weeks, BCVA was numerically better with FAR (0.20 vs. 0.49 logMAR; p = 0.08). CST reduction was sustained andcomparable (259 µm vs. 260 µm; p = 0.50). FAR achieved greater fvPED reduction (110 µm vs. 160 µm; p = 0.022). BRZ required fewer injections (6.3 vs. 7.2; p = 0.009) with similar intervals (9.4 vs. 9.9 weeks; p = 0.80). Mild IOI occurred in two BRZ eyes (4.9%) and none with FAR.

conclusionsIn poor-responsive nAMD, switching to BRZ or FAR under a TAE regimen without upload achieved stable vision, sustained CST reduction, and comparable treatment burden over one year. FAR showed greater fvPED regression and a slight functional trend, while BRZ achieved faster fluid resolution with fewer injections.

Indexed as

Antibodies, Monoclonal, HumanizedVisual AcuityWet Macular DegenerationAgedAngiogenesis InhibitorsAntibodies, BispecificDrug SubstitutionFemaleFluorescein AngiographyFollow-Up StudiesFundus OculiHumansIntravitreal InjectionsMaleRanibizumabRetrospective StudiesAngiogenesis InhibitorsAntibodies, BispecificAntibodies, Monoclonal, HumanizedbrolucizumabfaricimabRanibizumabVascular Endothelial Growth Factor AAnti-VEGF switchBrolucizumabFaricimabNeovascular age-related macular degenerationReal-worldTreat-and-extend

Identifiers

PMID41524752
PMCPMC13091869

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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.