Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema

被引:1294
作者
Wells, John A. [1 ]
Glassman, Adam R. [2 ]
Ayala, Allison R. [2 ]
Jampol, Lee M. [3 ]
Aiello, Lloyd Paul [4 ]
Antoszyk, Andrew N. [5 ]
Arnold-Bush, Bambi [2 ]
Baker, Carl W. [6 ]
Bressler, Neil M. [7 ]
Browning, David J. [5 ]
Elman, Michael J. [8 ]
Ferris, Frederick L. [9 ]
Friedman, Scott M. [10 ]
Melia, Michele [2 ]
Pieramici, Dante J. [11 ]
Sun, Jennifer K. [4 ]
Beck, Roy W. [2 ]
机构
[1] Palmetto Retina Ctr, W Columbia, SC USA
[2] Jaeb Ctr Hlth Res, Tampa, FL 33647 USA
[3] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[4] Harvard Univ, Sch Med, Beetham Eye Inst, Joslin Diabet Ctr, Boston, MA USA
[5] Charlotte Eye Ear Nose & Throat Associates, Charlotte, NC USA
[6] Paducah Retinal Ctr, Paducah, KY USA
[7] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
[8] Elman Retina Grp, Baltimore, MD USA
[9] NEI, NIH, Bethesda, MD 20892 USA
[10] Florida Retina Consultants, Lakeland, FL USA
[11] Calif Retina Consultants, Santa Barbara, CA USA
基金
美国国家卫生研究院;
关键词
ENDOTHELIAL GROWTH-FACTOR; RETINA STUDY-GROUP; INTRAVITREAL BEVACIZUMAB; RETINOPATHY; PREVALENCE; RISK;
D O I
10.1056/NEJMoa1414264
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The relative efficacy and safety of intravitreous aflibercept, bevacizumab, and ranibizumab in the treatment of diabetic macular edema are unknown. METHODS At 89 clinical sites, we randomly assigned 660 adults (mean age, 61 +/- 10 years) with diabetic macular edema involving the macular center to receive intravitreous aflibercept at a dose of 2.0 mg (224 participants), bevacizumab at a dose of 1.25 mg (218 participants), or ranibizumab at a dose of 0.3 mg (218 participants). The study drugs were administered as often as every 4 weeks, according to a protocol-specified algorithm. The primary outcome was the mean change in visual acuity at 1 year. RESULTS From baseline to 1 year, the mean visual-acuity letter score (range, 0 to 100, with higher scores indicating better visual acuity; a score of 85 is approximately 20/20) improved by 13.3 with aflibercept, by 9.7 with bevacizumab, and by 11.2 with ranibizumab. Although the improvement was greater with aflibercept than with the other two drugs (P<0.001 for aflibercept vs. bevacizumab and P = 0.03 for aflibercept vs. ranibizumab), it was not clinically meaningful, because the difference was driven by the eyes with worse visual acuity at baseline (P<0.001 for interaction). When the initial visual-acuity letter score was 78 to 69 (equivalent to approximately 20/32 to 20/40) (51% of participants), the mean improvement was 8.0 with aflibercept, 7.5 with bevacizumab, and 8.3 with ranibizumab (P>0.50 for each pairwise comparison). When the initial letter score was less than 69 (approximately 20/50 or worse), the mean improvement was 18.9 with aflibercept, 11.8 with bevacizumab, and 14.2 with ranibizumab (P<0.001 for aflibercept vs. bevacizumab, P = 0.003 for aflibercept vs. ranibizumab, and P = 0.21 for ranibizumab vs. bevacizumab). There were no significant differences among the study groups in the rates of serious adverse events (P = 0.40), hospitalization (P = 0.51), death (P = 0.72), or major cardiovascular events (P = 0.56). CONCLUSIONS Intravitreous aflibercept, bevacizumab, or ranibizumab improved vision in eyes with center-involved diabetic macular edema, but the relative effect depended on baseline visual acuity. When the initial visual-acuity loss was mild, there were no apparent differences, on average, among study groups. At worse levels of initial visual acuity, aflibercept was more effective at improving vision.
引用
收藏
页码:1193 / 1203
页数:11
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