英文摘要 |
Recent advances in target therapy have led to breakthroughs in ophthalmology, revolutionizing the treatment landscape. Among them, anti-VEGF drugs play one of the most important roles in the management of retinal diseases. Through intravitreal injection, target therapy agents could be directly applied to the retina, minimizing systemic side-effects. Since studies discovered the critical role of abnormal VEGF signaling in numerous retinal diseases, such as neovascular age related macular degeneration (nAMD), diabetic macular edema, and retinal vein occlusions, VEGF inhibition has been established as a highly effective treatment and significantly improved the outcome of these patients. Yet what comes along with the success are the new problems that come to the fore. The administration of these target therapy requires repeated visits for imaging, examination and injections, over a long period of time, which is a heavy burden for both patients and physicians. Despite clinical studies demonstrated the benefit of anti-VEGF target therapy in treating retinal diseases, there is still a group of poor responders that should not be overlooked. Therefore, the availability of biomarkers to guide the treatment protocol for patients, as well as the development of new drugs with longer half-life or multiple targets are the current main focus of drug development. While these drugs hold great promise in terms of efficacy, some toxic side-effects could not be completely avoided even with local administration of the drugs, despite intraocular injection reduces the risk of systemic drug exposure. On the other hand, advances in other novel target therapy drugs such as immunotherapies for cancer are not without their risks, including potentially ocular toxicity linked to the drugs' mechanism of action. |