2022
DOI: 10.1097/iae.0000000000003310
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Efficacy and Safety of Aflibercept for the Treatment of Idiopathic Choroidal Neovascularization in Young Patients

Abstract: Purpose: To evaluate the mean change in visual acuity at 52 weeks in patients with idiopathic choroidal neovascularization treated with aflibercept.Methods: We conducted a prospective noncomparative open-label Phase-II trial. The dosage regimen evaluated in this study was structured into two periods: (1) from inclusion to 20 weeks: a treat-and-extend period composed of three mandatory intravitreal injections, and complementary intravitreal injections performed if needed; (2) from 21 weeks to 52 weeks: a pro re… Show more

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Cited by 4 publications
(5 citation statements)
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“…There were no serious side effects related to IVA injection. In congruence with the safety reports of IVA by Korol et al [ 12 ], Gliem et al [ 13 ], and the INTUITION study [ 8 ], we did not detect any ocular or systemic side effects associated with IVA injection in the present study. Our results corroborate those of the fore-mentioned studies and support the notion that the damage induced to the RPE-Bruch’s membrane complex by certain fundus disorders with secondary CNV formation is self-limiting compared to the chronic progressive pathology of nAMD [ 14 ].…”
Section: Discussionsupporting
confidence: 92%
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“…There were no serious side effects related to IVA injection. In congruence with the safety reports of IVA by Korol et al [ 12 ], Gliem et al [ 13 ], and the INTUITION study [ 8 ], we did not detect any ocular or systemic side effects associated with IVA injection in the present study. Our results corroborate those of the fore-mentioned studies and support the notion that the damage induced to the RPE-Bruch’s membrane complex by certain fundus disorders with secondary CNV formation is self-limiting compared to the chronic progressive pathology of nAMD [ 14 ].…”
Section: Discussionsupporting
confidence: 92%
“…None of the patients enrolled in the study had serious side effects related to IVA. The INTUITION study [ 8 ] reported a series of 16 patients with idiopathic CNV. The treatment protocol included a loading dose of 3 IVA injections followed by a treat-and-extend (TER) regimen up to week 20.…”
Section: Discussionmentioning
confidence: 99%
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“…There were no reports of ocular serious adverse, and a few non‐ocular serious adverse events were reported, unrelated to the study drug or protocol. The safety profile of our study was in accordance with previously published studies (Heier et al, 2012; Ikuno et al, 2015; Kodjikian et al, 2022).…”
Section: Discussionsupporting
confidence: 91%
“…The earliest possible diagnosis of AMD and its neovascular complication allows for prompt treatment of the disease with intravitreal injections of anti-VEGF. Many studies have proved the efficacy and safety of bevacizumab, ranibizumab, and aflibercept in treating neovascular AMD [2,3,8] and other related diseases [9,10]. However, some differences in visual gain and anatomical outcomes exist between series, which appear to be associated with the baseline patient and disease characteristics and the treatment regimen used.…”
mentioning
confidence: 99%