Vascular Endothelial Growth Factor Trap-Eye for Macular Edema Secondary to Central Retinal Vein Occlusion Six-Month Results of the Phase 3 COPERNICUS Study

被引:196
作者
Boyer, David [2 ]
Heier, Jeffrey [3 ]
Brown, David M. [4 ]
Clark, W. Lloyd [5 ]
Vitti, Robert [6 ]
Berliner, Alyson J. [6 ]
Groetzbach, Georg [7 ]
Zeitz, Oliver [7 ,8 ]
Sandbrink, Rupert [7 ,9 ]
Zhu, Xiaoping [6 ]
Beckmann, Karola [7 ]
Haller, Julia A. [1 ]
机构
[1] Wills Eye Inst, Philadelphia, PA 19107 USA
[2] Retina Vitreous Associates Med Grp, Los Angeles, CA USA
[3] Ophthalm Consultants Boston, Boston, MA USA
[4] Methodist Hosp, Retina Consultants Houston, Houston, TX 77030 USA
[5] Palmetto Retina Ctr, W Columbia, SC USA
[6] Regeneron Pharmaceut Inc, Tarrytown, NY USA
[7] Bayer Healthcare, Berlin, Germany
[8] Dept Univ Klinikum Hamburg Eppendorf, Klin & Poliklin Augenheilkunde, Hamburg, Germany
[9] Univ Dusseldorf, Dept Neurol, Dusseldorf, Germany
关键词
VEGF; PREVALENCE;
D O I
10.1016/j.ophtha.2012.01.042
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
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 mu m in eyes treated with VEGF Trap-Eye versus 144.8 mu m 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.
引用
收藏
页码:1024 / 1032
页数:9
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