Switching from Aflibercept to Faricimab in the Treatment of Neovascular Age-Related Macular Degeneration: Short-Term Results from Real-Life Study

<b>Purpose:</b> To evaluate anatomical and functional outcomes after switching from aflibercept to faricimab in patients with neovascular age-related macular degeneration (nAMD) with suboptimal response. <b>Methods:</b> This retrospective study included 72 eyes of 66 patients with nAMD previously treated with intravitreal aflibercept using a treat-and-extend regimen. Indications for switching included persistent retinal fluid, pigment epithelial detachment (PED), lack of best-corrected visual acuity (BCVA) improvement, or inability to extend treatment intervals beyond four weeks. Patients received three monthly loading doses of faricimab followed by individualized 8- to 16-week dosing. Follow-up comprised six visits over a mean of 8.5 ± 1.4 months. Outcomes included BCVA (logMAR), retinal morphology (subretinal fluid-SRF; intraretinal fluid-IRF; pigment epithelial detachment-PED), central subfoveal thickness (CST), and treatment interval changes. <b>Results:</b> Switching to faricimab led to significant short-term anatomical improvement, primarily reduction in subretinal fluid (<i>p</i> < 0.0001), with maximal effect during the loading phase. Resolution of SRF was significant at the end of the follow up; however, IRF changes were transient and not sustained beyond three months. PED reduction reached borderline significance (<i>p</i> = 0.0455). CST decreased during the loading phase (<i>p</i> < 0.0001) but returned to baseline thereafter. BCVA improved only after loading (<i>p</i> = 0.0287) but not at final follow-up. Treatment intervals were extended by a mean of ~2 weeks (<i>p</i> < 0.0001), increasing in 80% of eyes. Eyes with fewer prior injections and better baseline BCVA achieved superior final visual outcomes. <b>Conclusions:</b> Switching to faricimab provides short-term anatomical benefits and treatment-interval extension without sustained visual gain. Functional improvements tended to be greater in patients with fewer injections and shorter treatment duration prior to switch.

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Publication Details

Journal
Journal of Clinical Medicine
Published
2025-10-17
DOI
https://doi.org/10.3390/jcm14207345
Citations
1
Primary Topic
Retinal Diseases and Treatments
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article
Field-Weighted Citation Impact
1.71
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article

Switching from Aflibercept to Faricimab in the Treatment of Neovascular Age-Related Macular Degeneration: Short-Term Results from Real-Life Study

H Kasprzak, Jan Kucharczuk, Maciej Gawęcki
1 citations
Journal of Clinical Medicine
Retinal Diseases and Treatments
1.71
article

Switching from Aflibercept to Faricimab in the Treatment of Neovascular Age-Related Macular Degeneration: Short-Term Results from Real-Life Study

H Kasprzak, Jan Kucharczuk, Maciej Gawęcki
article en
1 citations

Abstract

<b>Purpose:</b> To evaluate anatomical and functional outcomes after switching from aflibercept to faricimab in patients with neovascular age-related macular degeneration (nAMD) with suboptimal response. <b>Methods:</b> This retrospective study included 72 eyes of 66 patients with nAMD previously treated with intravitreal aflibercept using a treat-and-extend regimen. Indications for switching included persistent retinal fluid, pigment epithelial detachment (PED), lack of best-corrected visual acuity (BCVA) improvement, or inability to extend treatment intervals beyond four weeks. Patients received three monthly loading doses of faricimab followed by individualized 8- to 16-week dosing. Follow-up comprised six visits over a mean of 8.5 ± 1.4 months. Outcomes included BCVA (logMAR), retinal morphology (subretinal fluid-SRF; intraretinal fluid-IRF; pigment epithelial detachment-PED), central subfoveal thickness (CST), and treatment interval changes. <b>Results:</b> Switching to faricimab led to significant short-term anatomical improvement, primarily reduction in subretinal fluid (<i>p</i> < 0.0001), with maximal effect during the loading phase. Resolution of SRF was significant at the end of the follow up; however, IRF changes were transient and not sustained beyond three months. PED reduction reached borderline significance (<i>p</i> = 0.0455). CST decreased during the loading phase (<i>p</i> < 0.0001) but returned to baseline thereafter. BCVA improved only after loading (<i>p</i> = 0.0287) but not at final follow-up. Treatment intervals were extended by a mean of ~2 weeks (<i>p</i> < 0.0001), increasing in 80% of eyes. Eyes with fewer prior injections and better baseline BCVA achieved superior final visual outcomes. <b>Conclusions:</b> Switching to faricimab provides short-term anatomical benefits and treatment-interval extension without sustained visual gain. Functional improvements tended to be greater in patients with fewer injections and shorter treatment duration prior to switch.

Journal of Clinical MedicineVol. 14(20)
Military Hospital (PK), 1 Military Clinical Hospital with Outpatient Clinic (PL), Gdańsk Medical University (PL)
Openalex Percentile: Top 13%
Retinal Diseases and Treatments
1.71
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