Abstract |
PurposeTo investigate 1-year visual and anatomic outcomes of intravitreal aflibercept for neovascular age-related macular degeneration (nAMD) given at a fixed 8-weekly interval.MethodsRetrospective, single-practice data analysis from an electronic medical record system of 255 eyes (223 patients) with treatment-naïve nAMD receiving 8-weekly aflibercept.ResultsMean logarithm of the minimum angle of resolution best-corrected visual acuity (BCVA) improved from 0.66 at baseline to 0.50 at month 11 (P<0.0001). Mean central retinal thickness (CRT) decreased from 311 μm at baseline to 211 μm at month 11 (P<0.0001). Our mean VA gain of eight ETDRS letters was comparable to the VIEW 1 and VIEW 2 Trials' results at the end of year 1. After loading at month 5, mean BCVA was 0.48 (P<0.0001), and mean CRT was 235 μm. At month 5, 143 eyes (56%) were inactive defined by the absence of macular haemorrhage and intraretinal fluid (IRF) and subretinal fluid (SRF) on optical coherence tomography, and 112 eyes (44%) remained active. At month 11, 136 eyes (53%) were inactive, and 119 eyes (47%) remained active. At month 11, 77% of inactive eyes after loading remained inactive, and 77% of the active eyes after loading remained active. At month 11, mean BCVA of the inactive group was 0.51, and mean BCVA of the active group was 0.48 (P=0.54).ConclusionsAflibercept administered by fixed dosing over 1 year improved VA and macular morphology in treatment-naïve eyes. Active lesions at month 11 do not have worse VA outcomes compared with inactive lesions. The macular status after loading is a reliable indicator of disease activity at the end of year 1.
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Authors | H Almuhtaseb, S Kanavati, S R Rufai, A J Lotery |
Journal | Eye (London, England)
(Eye (Lond))
Vol. 31
Issue 6
Pg. 878-883
(Jun 2017)
ISSN: 1476-5454 [Electronic] England |
PMID | 28186507
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Recombinant Fusion Proteins
- aflibercept
- Receptors, Vascular Endothelial Growth Factor
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Topics |
- Aged, 80 and over
- Dose-Response Relationship, Drug
- Drug Administration Schedule
- Female
- Fluorescein Angiography
- Follow-Up Studies
- Fundus Oculi
- Humans
- Intravitreal Injections
- Male
- Receptors, Vascular Endothelial Growth Factor
(administration & dosage, antagonists & inhibitors)
- Recombinant Fusion Proteins
(administration & dosage)
- Retina
(pathology)
- Retrospective Studies
- Tomography, Optical Coherence
- Treatment Outcome
- Visual Acuity
- Wet Macular Degeneration
(diagnosis, drug therapy, physiopathology)
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