TY - JOUR
T1 - Vascular endothelial growth factor Trap-Eye for macular edema secondary to central retinal vein occlusion
T2 - Six-month results of the phase 3 COPERNICUS study
AU - Boyer, David
AU - Heier, Jeffrey
AU - Brown, David M.
AU - Clark, W. Lloyd
AU - Vitti, Robert
AU - Berliner, Alyson J.
AU - Groetzbach, Georg
AU - Zeitz, Oliver
AU - Sandbrink, Rupert
AU - Zhu, Xiaoping
AU - Beckmann, Karola
AU - Haller, Julia A.
N1 - Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2012/5
Y1 - 2012/5
N2 - Objective: To assess the efficacy and safety of intravitreal vascular endothelial growth factor (VEGF) Trap-Eye in eyes with macular edema secondary to central retinal vein occlusion (CRVO). Design: Multicenter, randomized, prospective, controlled trial. Participants: One hundred eighty-nine eyes with macular edema secondary to CRVO. Methods: Eyes were randomized 3:2 to receive VEGF Trap-Eye 2 mg or sham injection monthly for 6 months. Main Outcome Measures: The proportion of eyes with a <15-letter gain or more in best-corrected visual acuity (BCVA) at week 24 (primary efficacy end point), mean changes in BCVA and central retinal thickness (CRT), and proportion of eyes progressing to neovascularization of the anterior segment, optic disc, or elsewhere in the retina. Results: At week 24, 56.1% of VEGF Trap-Eye treated eyes gained 15 letters or more from baseline versus 12.3% of sham-treated eyes (P<0.001). The VEGF Trap-Eye treated eyes gained a mean of 17.3 letters versus sham-treated eyes, which lost 4.0 letters (P<0.001). Central retinal thickness decreased by 457.2 μm in eyes treated with VEGF Trap-Eye versus 144.8 μm in sham-treated eyes (P<0.001), and progression to any neovascularization occurred in 0 and 5 (6.8%) of eyes treated with VEGF Trap-Eye and sham-treated eyes, respectively (P = 0.006). Conjunctival hemorrhage, reduced visual acuity, and eye pain were the most common adverse events (AEs). Serious ocular AEs were reported by 3.5% of VEGF Trap-Eye patients and 13.5% of sham patients. Incidences of nonocular serious AEs generally were well balanced between both groups. Conclusions: At 24 weeks, monthly intravitreal injection of VEGF Trap-Eye 2 mg in eyes with macular edema resulting from CRVO improved visual acuity and CRT, eliminated progression resulting from neovascularization, and was associated with a low rate of ocular AEs related to treatment. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.
AB - Objective: To assess the efficacy and safety of intravitreal vascular endothelial growth factor (VEGF) Trap-Eye in eyes with macular edema secondary to central retinal vein occlusion (CRVO). Design: Multicenter, randomized, prospective, controlled trial. Participants: One hundred eighty-nine eyes with macular edema secondary to CRVO. Methods: Eyes were randomized 3:2 to receive VEGF Trap-Eye 2 mg or sham injection monthly for 6 months. Main Outcome Measures: The proportion of eyes with a <15-letter gain or more in best-corrected visual acuity (BCVA) at week 24 (primary efficacy end point), mean changes in BCVA and central retinal thickness (CRT), and proportion of eyes progressing to neovascularization of the anterior segment, optic disc, or elsewhere in the retina. Results: At week 24, 56.1% of VEGF Trap-Eye treated eyes gained 15 letters or more from baseline versus 12.3% of sham-treated eyes (P<0.001). The VEGF Trap-Eye treated eyes gained a mean of 17.3 letters versus sham-treated eyes, which lost 4.0 letters (P<0.001). Central retinal thickness decreased by 457.2 μm in eyes treated with VEGF Trap-Eye versus 144.8 μm in sham-treated eyes (P<0.001), and progression to any neovascularization occurred in 0 and 5 (6.8%) of eyes treated with VEGF Trap-Eye and sham-treated eyes, respectively (P = 0.006). Conjunctival hemorrhage, reduced visual acuity, and eye pain were the most common adverse events (AEs). Serious ocular AEs were reported by 3.5% of VEGF Trap-Eye patients and 13.5% of sham patients. Incidences of nonocular serious AEs generally were well balanced between both groups. Conclusions: At 24 weeks, monthly intravitreal injection of VEGF Trap-Eye 2 mg in eyes with macular edema resulting from CRVO improved visual acuity and CRT, eliminated progression resulting from neovascularization, and was associated with a low rate of ocular AEs related to treatment. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.
UR - http://www.scopus.com/inward/record.url?scp=84862779327&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862779327&partnerID=8YFLogxK
U2 - 10.1016/j.ophtha.2012.01.042
DO - 10.1016/j.ophtha.2012.01.042
M3 - Article
C2 - 22440275
AN - SCOPUS:84862779327
SN - 0161-6420
VL - 119
SP - 1024
EP - 1032
JO - Ophthalmology
JF - Ophthalmology
IS - 5
ER -