Neovascular Age-Related Macular Degeneration (nAMD): A Review of Emerging Treatment Options

被引:49
|
作者
Tan, Colin S. [1 ,2 ]
Ngo, Wei Kiong [1 ,2 ]
Chay, Isaac W. [1 ,2 ]
Ting, Dominic S. [1 ,2 ]
Sadda, SriniVas R. [3 ]
机构
[1] Tan Tock Seng Hosp, Natl Healthcare Grp Eye Inst, Singapore, Singapore
[2] Natl Healthcare Grp Eye Inst, Fundus Image Reading Ctr, Singapore, Singapore
[3] Doheny Eye Inst, Doheny Image Reading Ctr, 3623,1450 San Pablo St, Los Angeles, CA 90033 USA
来源
CLINICAL OPHTHALMOLOGY | 2022年 / 16卷
基金
英国医学研究理事会;
关键词
neovascular AMD; anti-VEGF; retina; gene therapy; ENDOTHELIAL GROWTH-FACTOR; GENE-THERAPY; CHOROIDAL NEOVASCULARIZATION; INCREASED EXPRESSION; TRANSGENIC MICE; RANIBIZUMAB; VERTEPORFIN; BEVACIZUMAB; EFFICACY; OUTCOMES;
D O I
10.2147/OPTH.S231913
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Neovascular age-related macular degeneration (nAMD) is a common world-wide cause of visual loss. Intravitreal anti-vascular endothelial growth factor (anti-VEGF) agents are an effective means to treat nAMD and reduce its impact on vision compared to either sham treatment or photodynamic therapy. Currently, the approved anti-VEGF drugs include ranibizumab, aflibercept and brolucizumab. In addition, bevacizumab, used as an off-label drug, and has been shown to be effective in treating nAMD. While anti-VEGF agents are effective, its limitations include the requirement for frequent, often monthly injections, and the need for long-term treatment of nAMD. These present significant burdens on the healthcare system and on the patients. In addition, reviews of patients with nAMD treated with anti-VEGF have reported deterioration of vision over time with progression of geographic atrophy. These limitations are partly addressed by exploring different treatment regimens that reduce the frequency of treatments. Newer anti-VEGF drugs have been shown in Phase III clinical trials to have injection intervals as long as 12 or even 16 weeks for a proportion of patients. There is research on newer drugs that affect other pathways, such as the angiopoietin pathway, which may impact nAMD by extending the treatment interval and reducing the burden of treatment. Other measures include the use of sustained-release implants that release the drug regularly over a period of time, and can be refilled periodically, as well as hydrogel platforms that serve to release the drug. The use of biosimilars will also serve to reduce the cost of treatment for nAMD. A new frontier of gene therapy, primarily targeting genes involved in the transduction of retinal cells to produce anti-VEGF proteins intraocularly, also opens a new avenue of therapeutic approaches that can be used for treatment. This review paper will discuss both current treatment options and the newer treatments under development.
引用
收藏
页码:917 / 933
页数:17
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