Treatment outcomes of switching to aflibercept 8 mg in previously-treated neovascular age-related macular degeneration
摘要
To evaluate outcomes of switching to aflibercept 8 mg in eyes with neovascular age-related macular degeneration (nAMD) previously treated with anti-vascular endothelial growth factor (VEGF) agents.
MethodsThis multicenter retrospective study examined 6-month treatment outcomes in eyes with nAMD previously treated and switched to aflibercept 8 mg. Data including best-corrected visual acuity (BCVA), number of previous injections, and treatment intervals were collected. Central retinal thickness (CRT), subfoveal choroidal thickness (SFCT), and maximal pigment epithelial detachment (PED) height were measured on optical coherence tomography images.
ResultsAnalysis included 121 eyes (117 patients). Median number of previous anti-VEGF injections was 31.0 (interquartile range [IQR]: 20.5–55.5); median pre-switch interval was 5.0 (IQR: 4.0–8.0) weeks. At 6 months, 71 eyes (59%) continued aflibercept 8 mg and 50 (41%) discontinued due to worsening at intervals ≥ 8 weeks. The discontinued group had significantly shorter pre-switch intervals (4.0 [IQR: 4.0–5.0] vs. 6.0 [IQR: 5.0–8.0], P < 0.01) and thinner SFCT compared to the continued group (153 [IQR: 100–209] vs. 189 [IQR: 141–284], P = 0.012). At 6 months, CRT and PED decreased from 258 (IQR: 203–329) to 239 (IQR: 198–304) µm (P = 0.015) and from 195 (IQR: 112–293) to 164 (IQR: 82–263) µm (P = 0.007). BCVA was maintained (0.15 [IQR: 0.00–0.30] to 0.10 [IQR: 0.00–0.30]), P = 0.426). The median increase in injection interval was 2.0 (IQR: 1.0–3.5) weeks in continued eyes.
ConclusionSwitching to aflibercept 8 mg may be an option to extend injection intervals, leading to a reduction in treatment burden.