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Clinical Trial
. 2012 Dec;119(12):2537-48.
doi: 10.1016/j.ophtha.2012.09.006. Epub 2012 Oct 17.

Intravitreal aflibercept (VEGF trap-eye) in wet age-related macular degeneration

Affiliations
Clinical Trial

Intravitreal aflibercept (VEGF trap-eye) in wet age-related macular degeneration

Jeffrey S Heier et al. Ophthalmology. 2012 Dec.

Erratum in

  • Ophthalmology. 2013 Jan;120(1):209-10

Abstract

Objective: Two similarly designed, phase-3 studies (VEGF Trap-Eye: Investigation of Efficacy and Safety in Wet AMD [VIEW 1, VIEW 2]) of neovascular age-related macular degeneration (AMD) compared monthly and every-2-month dosing of intravitreal aflibercept injection (VEGF Trap-Eye; Regeneron, Tarrytown, NY, and Bayer HealthCare, Berlin, Germany) with monthly ranibizumab.

Design: Double-masked, multicenter, parallel-group, active-controlled, randomized trials.

Participants: Patients (n = 2419) with active, subfoveal, choroidal neovascularization (CNV) lesions (or juxtafoveal lesions with leakage affecting the fovea) secondary to AMD.

Intervention: Patients were randomized to intravitreal aflibercept 0.5 mg monthly (0.5q4), 2 mg monthly (2q4), 2 mg every 2 months after 3 initial monthly doses (2q8), or ranibizumab 0.5 mg monthly (Rq4).

Main outcome measures: The primary end point was noninferiority (margin of 10%) of the aflibercept regimens to ranibizumab in the proportion of patients maintaining vision at week 52 (losing <15 letters on Early Treatment Diabetic Retinopathy Study [ETDRS] chart). Other key end points included change in best-corrected visual acuity (BCVA) and anatomic measures.

Results: All aflibercept groups were noninferior and clinically equivalent to monthly ranibizumab for the primary end point (the 2q4, 0.5q4, and 2q8 regimens were 95.1%, 95.9%, and 95.1%, respectively, for VIEW 1, and 95.6%, 96.3%, and 95.6%, respectively, for VIEW 2, whereas monthly ranibizumab was 94.4% in both studies). In a prespecified integrated analysis of the 2 studies, all aflibercept regimens were within 0.5 letters of the reference ranibizumab for mean change in BCVA; all aflibercept regimens also produced similar improvements in anatomic measures. Ocular and systemic adverse events were similar across treatment groups.

Conclusions: Intravitreal aflibercept dosed monthly or every 2 months after 3 initial monthly doses produced similar efficacy and safety outcomes as monthly ranibizumab. These studies demonstrate that aflibercept is an effective treatment for AMD, with the every-2-month regimen offering the potential to reduce the risk from monthly intravitreal injections and the burden of monthly monitoring.

Financial disclosure(s): Proprietary or commercial disclosure may be found after the references.

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Comment in

  • Author reply: To PMID 23084240.
    Heier JS, Brown DM, Chong V, Korobelnik JF, Kaiser PK, Nguyen QD, Kirchhof B, Ho A, Ogura Y, Schmidt-Erfurth U. Heier JS, et al. Ophthalmology. 2014 Jan;121(1):e5-6. doi: 10.1016/j.ophtha.2013.09.018. Epub 2013 Nov 18. Ophthalmology. 2014. PMID: 24256893 No abstract available.
  • Safety in Aflibercept versus Ranibizumab.
    Ueta T. Ueta T. Ophthalmology. 2014 Jan;121(1):e5. doi: 10.1016/j.ophtha.2013.09.019. Epub 2013 Nov 18. Ophthalmology. 2014. PMID: 24256894 No abstract available.
  • Is there risk of stroke with aflibercept?
    Beaumont PE, Petocz P, Kang HK. Beaumont PE, et al. Ophthalmology. 2014 Jan;121(1):e4. doi: 10.1016/j.ophtha.2013.09.020. Epub 2013 Nov 20. Ophthalmology. 2014. PMID: 24268853 No abstract available.
  • Author reply: To PMID 23084240.
    Heier JS, Brown DM, Chong V, Korobelnik JF, Kaiser PK, Nguyen QD, Kirchhof B, Ho A, Ogura Y, Schmidt-Erfurth U. Heier JS, et al. Ophthalmology. 2014 Jan;121(1):e5-e6. Ophthalmology. 2014. PMID: 24536092 No abstract available.

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