Evidence map›Paper›PMID 40133689›Full record

ArticleOphthalmology and therapy2025

Deep-Learning-Assisted Analysis of Early Biomarker Changes in Treatment-Naïve Patients with Neovascular AMD Under Intravitreal Faricimab.

Michael Hafner, Ben Asani, Franziska Eckardt, Jakob Siedlecki, Benedikt Schworm, Siegfried G Priglinger, Johannes Schiefelbein

Abstract read
In one paragraph

Article in Ophthalmology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

7 authors.

Michael Hafner *Department of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany. Michael.Hafner@med.uni-muenchen.de.ORCID http://orcid.org/0009-0008-9025-259X
Ben Asani *Department of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.
Franziska EckardtDepartment of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.
Jakob SiedleckiDepartment of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.
Benedikt SchwormDepartment of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.
Siegfried G PriglingerDepartment of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.
Johannes SchiefelbeinDepartment of Ophthalmology, LMU University Hospital, LMU Munich, Mathildenstraße 8, 80336, Munich, Germany.

Funding

Bundesministerium für Bildung und Forschung 031L0210AHelmholtz Association ZT-I-PF-5-01
6 · The paper itself

Abstract

introductionArtificial intelligence (AI)-driven biomarker segmentation offers an objective approach to assessing neovascular age-related macular degeneration (nAMD). In addition, faricimab, a bispecific VEGF and Ang-2 inhibitor, presents new potential in disease management. This study applies an AI-based segmentation algorithm to quantify key optical coherence tomography (OCT) biomarkers and assess the short-term efficacy of intravitreal faricimab in treatment-naïve patients.

methodsThis retrospective analysis includes 40 eyes from 38 treatment-naïve patients with nAMD treated with faricimab at LMU University Hospital Munich between January 2023 and September 2024. Patients received 4-monthly intravitreal injections. Biomarkers of disease activity, including central retinal thickness (CRT), intraretinal fluid (IRF), subretinal fluid (SRF), subretinal hyperreflective material (SHRM) and fibrovascular pigment epithelium detachment (fvPED), were quantified using a deep learning-based semantic segmentation algorithm. Best-corrected visual acuity (BCVA) and OCT imaging data were analyzed at baseline (mo0) and after 1 (mo1), 2 (mo2) and 3 months (mo3).

resultsAI-driven analysis revealed significant reductions in key biomarkers. CRT decreased from 433.6 (IQR: 306.6) µm at mo0 to 241.5 (IQR: 130.8) µm at mo3 (p < 0.0001). IRF and SRF volumes were reduced by > 99% from mo0 to mo3 (both p < 0.0001). BCVA improved from 0.60 (IQR: 0.30) logMAR at mo0 to 0.40 (IQR: 0.33) logMAR at mo3 (p < 0.0001). Correlation analysis identified IRF and SHRM reductions as the strongest predictors of visual improvement.

conclusionThis study demonstrates the potential of AI-assisted biomarker analysis for precise disease monitoring in nAMD. Faricimab significantly reduced disease activity biomarkers and improved visual acuity in treatment-naïve patients, reinforcing its efficacy in early disease control. Future studies should explore long-term outcomes and further integrate AI-driven biomarker evaluation in clinical practice.

Indexed as

Artificial intelligenceBiomarkerFaricimabNeovascular age-related macular degeneration (nAMD)Real-world data

Identifiers

PMID40133689
PMCPMC12006649

What Socratic holds

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Registered trials

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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 Socratic graph.