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296 posters, 7 videos, 13 audios, 14 topics, 10 sessions, 1,019 authors, 259 institutions

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RCOphth Annual Congress 2026

18 - 21 May, 2026 | Manchester Central, Manchester

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P150

Comparing outcomes of faricimab and aflibercept therapy in treatment-na?ve patients with diabetic macular oedema at the Oxford Eye Hospital

Part of Topic

Medical retina

Introduction

Faricimab (Vabysmo®) and aflibercept (Eylea®) are approved therapies for diabetic macular oedema (DMO) and inhibit VEGF-A; faricimab additionally targets angiopoietin-2, while aflibercept inhibits VEGF-B and placental growth factor1-3. We compared their real-world outcomes in treatment-naïve DMO patients.

 

Methods

Retrospective study at Oxford Eye Hospital of treatment-naïve DMO patients initiating faricimab or aflibercept (November 2022-March 2024). Included patients had ≥12 months follow-up. Visual acuity (VA), central subfield thickness (CST), and treatment interval were evaluated at baseline, 6 months (±8 weeks), 12 months (±8 weeks), and 18 months (±12 weeks). Linear mixed-effects modelling with subject as random intercept accounted for non-independent, longitudinal data. Missing data was handled through the linear mixed-effects model.

 

Results

99 eyes received faricimab and 78 aflibercept; baseline characteristics were comparable. VA remained stable in both groups with no significant between-group differences. Both agents reduced CST from baseline to six months, sustained thereafter, but faricimab achieved significantly greater CST reduction at 12 (p=0.02) and 18 months (p<0.01), a 2.75-week longer mean treatment interval at 12 months (p<0.01), and fewer injections across 18 months (p=0.04).

 

Discussion

Both agents stabilised VA and reduced CST in treatment-naïve DMO. Faricimab was associated with greater CST reduction and fewer injections over 18 months.

 

Table 1. Baseline characteristics of treatment-naïve patients with DMO at Oxford Eye Hospital treated with faricimab or aflibercept. Continuous variables: mean ± SD (Welch’s unpaired t-test); categorical variables: n (%) (Fisher’s exact test). No significant between-group differences at baseline. Early Treatment Diabetic Retinopathy Study (ETDRS), HbA1c (glycated haemoglobin).

 

Figure 1. Outcomes from linear mixed-effects modelling for faricimab (orange) and aflibercept (green), adjusted for baseline covariates. Error bars represent SEM. Between-group comparisons shown above each time point: ns = not significant (p≥0.05), *p<0.05, **p<0.01.

(A)Visual acuity: No significant between-group differences at any timepoint. VA remained stable in both groups.
(B)CST: Both drugs significantly reduced CST from baseline to 6 months. Faricimab achieved greater CST reduction at 12 and 18 months.
(C)Treatment interval: Faricimab-treated eyes had a significantly longer mean treatment interval at 12 months. 
 


Figure 2. Total intravitreal injections over 18 months in eyes with complete follow-up. Box plots show median, interquartile range, and range. Faricimab-treated eyes received significantly fewer injections (mean 10.1±1.9) than aflibercept-treated eyes (mean 11.0±1.8; p=0.04, Welch’s t-test). *p<0.05.

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