Enzendorfer Marie Louise, Tratnig-Frankl Merle, Eidenberger Anna, Schrittwieser Johannes, Kuchernig Lukas, Schmidt-Erfurth Ursula
Laboratory for Ophthalmic Image Analysis, Department of Ophthalmology and Optometry, Medical University of Vienna, 1090 Vienna, Austria.
Pharmaceuticals (Basel). 2025 Feb 20;18(3):284. doi: 10.3390/ph18030284.
Age-related macular degeneration (AMD) is a leading cause of blindness in the developed world. Due to an aging population, its prevalence is expected to increase, making novel and optimized therapy options imperative. However, both late-stage forms of the disease, neovascular AMD (nAMD) and geographic atrophy (GA), exhibit considerable variability in disease progression and treatment response, complicating the evaluation of therapeutic efficacy and making it difficult to design clinical trials that are both inclusive and statistically robust. Traditional trial designs frequently rely on generalized endpoints that may not fully capture the nuanced benefits of treatment, particularly in diseases like GA, where functional improvements can be gradual or subtle. Artificial intelligence (AI) has the potential to address these issues by identifying novel, condition-specific biomarkers or endpoints, enabling precise patient stratification and improving recruitment strategies. By providing an overview of the advances and application of AI-based optical coherence tomography analysis in the context of AMD clinical trials, this review highlights the transformative potential of AI in optimizing clinical trial outcomes for patients with nAMD or GA secondary to AMD.
年龄相关性黄斑变性(AMD)是发达国家失明的主要原因。由于人口老龄化,其患病率预计会上升,因此新型且优化的治疗方案势在必行。然而,该疾病的两种晚期形式,即新生血管性AMD(nAMD)和地图样萎缩(GA),在疾病进展和治疗反应方面表现出相当大的变异性,这使得治疗效果的评估变得复杂,也难以设计出既具有包容性又在统计学上可靠的临床试验。传统的试验设计通常依赖于通用的终点指标,这些指标可能无法完全捕捉到治疗的细微益处,尤其是在GA这类疾病中,功能改善可能是渐进的或细微的。人工智能(AI)有潜力通过识别新的、针对特定病症的生物标志物或终点指标来解决这些问题,从而实现精确的患者分层并改进招募策略。通过概述基于AI的光学相干断层扫描分析在AMD临床试验中的进展和应用,本综述强调了AI在优化nAMD或AMD继发GA患者的临床试验结果方面的变革潜力。