Intravitreal Aflibercept (VEGF Trap-Eye) in Wet Age-related Macular Degeneration

被引:2004
作者
Heier, Jeffrey S. [2 ,3 ]
Brown, David M. [4 ]
Chong, Victor [5 ]
Korobelnik, Jean-Francois [6 ]
Kaiser, Peter K. [7 ]
Quan Dong Nguyen [8 ]
Kirchhof, Bernd [9 ]
Ho, Allen [10 ]
Ogura, Yuichiro [11 ]
Yancopoulos, George D. [12 ]
Stahl, Neil [12 ]
Vitti, Robert [12 ]
Berliner, Alyson J. [12 ]
Soo, Yuhwen [12 ]
Anderesi, Majid [13 ]
Groetzbach, Georg [13 ]
Sommerauer, Bernd [13 ]
Sandbrink, Rupert [13 ,14 ]
Simader, Christian
Schmidt-Erfurth, Ursula [1 ]
机构
[1] Med Univ Vienna, Dept Ophthalmol, A-1090 Vienna, Austria
[2] Ophthalm Consultants Boston, Boston, MA USA
[3] Tufts Univ, Sch Med, Boston, MA 02111 USA
[4] Retina Consultants Houston, Houston, TX USA
[5] Univ Oxford, Oxford Eye Hosp, Oxford, England
[6] Univ Bordeaux 2, CHU Bordeaux, F-33076 Bordeaux, France
[7] Cole Eye Inst, Cleveland, OH USA
[8] Johns Hopkins Univ, Wilmer Eye Inst, Baltimore, MD 21218 USA
[9] Univ Cologne, D-50931 Cologne, Germany
[10] Wills Eye Hosp & Res Inst, Philadelphia, PA USA
[11] Nagoya City Univ, Nagoya, Aichi, Japan
[12] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
[13] Bayer HealthCare, Berlin, Germany
[14] Univ Dusseldorf, Dept Neurol, D-40225 Dusseldorf, Germany
关键词
SUBFOVEAL CHOROIDAL NEOVASCULARIZATION; RANDOMIZED CLINICAL-TRIAL; PHOTODYNAMIC THERAPY; RANIBIZUMAB; VERTEPORFIN; GROWTH; LESIONS;
D O I
10.1016/j.ophtha.2012.09.006
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
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. Ophthalmology 2012;119:2537-2548 (C) 2012 by the American Academy of Ophthalmology.
引用
收藏
页码:2537 / 2548
页数:12
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