The efficacy and safety of aflibercept and conbercept in diabetic macular edema

被引:56
作者
Cai, Siwei [1 ]
Yang, Qianhui [1 ]
Li, Xiaorong [1 ]
Zhang, Yan [1 ]
机构
[1] Tianjin Med Univ, Eye Hosp, Coll Optometry & Ophthalmol, Eye Inst, Tianjin 300384, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2018年 / 12卷
基金
中国国家自然科学基金;
关键词
diabetes; diabetic retinopathy; diabetic macular edema; therapy; aflibercept; conbercept; clinical trial; VEGF decoy receptor; ENDOTHELIAL GROWTH-FACTOR; ACETONIDE VITREOUS INSERTS; DOMAIN-CONTAINING RECEPTOR; VEGF TRAP-EYE; INTRAVITREAL AFLIBERCEPT; FUSION PROTEIN; DA VINCI; RANIBIZUMAB; BEVACIZUMAB; LASER;
D O I
10.2147/DDDT.S177192
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetic macular edema (DME) has shown an increasing prevalence during the past years and is the leading cause of diabetic retinopathy blindness. Traditional treatment modalities include laser and corticosteroid therapy, which, however, either act through unclear mechanisms or cause cataracts and elevated intraocular pressure. In recent years, as the pathogenic role of VEGF in DME has been well-recognized, the intravitreal injection of anti-VEGF drugs has become the first-line treatment of DME due to their great efficacy in improving visual acuity and mitigating macular edema. Advantages have been shown for aflibercept and conbercept, the two recombinant decoy receptors that can bind VEGF with high specificity and affinity, in DME treatment in clinical trials conducted both worldwide and in People's Republic of China. This review introduces the structural characteristics and molecular mechanisms of action of these two anti-VEGF drugs, and summarizes the clinical trials evaluating their efficacy and safety, with the hope to provide clues for designing optimal and personalized therapeutic regimens for DME patients.
引用
收藏
页码:3471 / 3483
页数:13
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