1st University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
General Hospital of Volos, Volos, Greece.
Adv Ther. 2022 Jan;39(1):5-32. doi: 10.1007/s12325-021-01949-7. Epub 2021 Nov 1.
Neovascular age-related macular degeneration (nAMD) represents a leading cause of irreversible visual loss affecting the quality of life of millions of elderly patients worldwide. Although the introduction of intravitreal injections with anti-vascular endothelial growth factors (anti-VEGF) agents has revolutionized the management of nAMD, their effectiveness and ultimate success are limited by several therapeutic challenges. Consequently, real-world efficacy appears significantly inferior to that reported by randomized controlled trials. Therefore, further innovative, long-term treatment options are essential to improve the prognosis and outcome of nAMD therapy.
Emerging pharmacological therapies for nAMD and those currently in clinical trials are reviewed and their mechanism of action, safety, and efficacy are discussed. The evidence presented herein has been collected from online databases PubMed, Cochrane library, and the ClinicalTrials.gov site.
A number of promising technologies and novel anti-VEGF therapies are currently being tested and some have already reached phase III trials. Anti-VEGF agents with enhanced durability and possibly efficacy, gene therapy, angiogenic targets, alternative drug delivery routes such as sustained delivery implants, drug carriers, and encapsulated cell technology are currently being explored. We briefly discuss the potential value of these options.
Several options may optimize future nAMD management. On the basis of current, albeit limited evidence, the most promising technology to reach clinical practice soon appears to be the sustained drug delivery options, which may improve visual outcome and reduce the socioeconomic burden of nAMD.
新生血管性年龄相关性黄斑变性(nAMD)是一种导致全球数百万老年患者视力丧失且无法恢复的主要疾病,严重影响生活质量。虽然抗血管内皮生长因子(anti-VEGF)药物的玻璃体腔内注射已经彻底改变了 nAMD 的治疗方式,但它们的有效性和最终疗效受到多种治疗挑战的限制。因此,实际疗效明显低于随机对照试验报道的结果。因此,需要进一步开发创新的、长期的治疗方法,以改善 nAMD 治疗的预后和结果。
对 nAMD 的新兴药物治疗方法和目前正在进行的临床试验进行了综述,并讨论了它们的作用机制、安全性和疗效。本文中的证据来自在线数据库 PubMed、Cochrane 图书馆和 ClinicalTrials.gov 网站。
目前正在测试许多有前途的技术和新型抗 VEGF 疗法,其中一些已经进入了 III 期临床试验。具有增强的持久性和潜在疗效的抗 VEGF 药物、基因治疗、血管生成靶点、替代药物输送途径,如持续药物输送植入物、药物载体和封装细胞技术,目前正在探索中。我们简要讨论了这些选择的潜在价值。
有几种选择可能会优化未来 nAMD 的治疗方式。基于目前有限的证据,最有希望很快进入临床实践的技术似乎是持续药物输送选择,这可能会改善视力结果并减轻 nAMD 的社会经济负担。