Kaiser Peter K
Vitreoretinal Department, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio 44106, USA.
Retina. 2009 Jun;29(6 Suppl):S15-7. doi: 10.1097/IAE.0b013e3181ad240c.
Clinical trials increasingly support the premise that inhibition of vascular endothelial growth factor is a viable but insufficient target for long-term control of age-related macular degeneration (AMD). Additional biologic therapies targeted at very specific steps in the proliferative signaling pathway are being actively sought as alternatives or adjunctive strategies for the treatment of AMD. This rapidly advancing area of drug development is particularly encouraging because of the growing appreciation for the redundancies and interrelationships between the molecular events. The complexity of this signaling pathway supports the development of combination treatments for optimal control of biologic functions.
越来越多的临床试验支持这样一个前提,即抑制血管内皮生长因子是长期控制年龄相关性黄斑变性(AMD)的一个可行但并不充分的靶点。目前正在积极寻找针对增殖信号通路中非常特定步骤的其他生物疗法,作为治疗AMD的替代或辅助策略。由于对分子事件之间的冗余和相互关系的认识不断增加,这个药物开发迅速发展的领域尤其令人鼓舞。该信号通路的复杂性支持联合治疗的开发,以实现对生物功能的最佳控制。