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一项关于潜在参与者对眼部基因治疗看法的跨国调查。

A multinational survey of potential participant perspectives on ocular gene therapy.

机构信息

Department of Optometry and Vision Sciences, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia.

Ophthalmology, Department of Surgery, University of Melbourne, Melbourne, VIC, Australia.

出版信息

Gene Ther. 2024 May;31(5-6):314-323. doi: 10.1038/s41434-024-00450-4. Epub 2024 Apr 2.

Abstract

Amidst rapid advancements in ocular gene therapy, understanding patient perspectives is crucial for shaping future treatment choices and research directions. This international cross-sectional survey evaluated knowledge, attitudes, and perceptions of ocular genetic therapies among potential recipients with inherited retinal diseases (IRDs). Survey instruments included the Attitudes to Gene Therapy-Eye (AGT-Eye), EQ-5D-5L, National Eye Institute Visual Functioning Questionnaire (NEI-VFQ-25), and Patient Attitudes to Clinical Trials (PACT-22) instruments. This study included 496 participant responses (89% adults with IRDs; 11% parents/guardians/carers) from 35 countries, with most from the United States of America (USA; 69%) and the United Kingdom (11%). Most participants (90%) indicated they would likely accept gene therapy if it was available, despite only 45% agreeing that they had good knowledge of gene therapy. The main sources of information were research registries (60% of participants) and the internet (61%). Compared to data from our recently published Australian national survey of people with IRDs (n = 694), USA respondents had higher knowledge of gene therapy outcomes, and Australian respondents indicated a higher perceived value of gene therapy treatments. Addressing knowledge gaps regarding outcomes and financial implications will be central to ensuring informed consent, promoting shared decision-making, and the eventual clinical adoption of genetic therapies.

摘要

在眼科基因治疗快速发展的背景下,了解患者的观点对于确定未来的治疗选择和研究方向至关重要。本国际横断面调查评估了遗传性视网膜疾病(IRDs)潜在受者对眼部基因治疗的知识、态度和看法。调查工具包括基因治疗眼部态度量表(AGT-Eye)、EQ-5D-5L、国家眼科研究所视觉功能问卷(NEI-VFQ-25)和患者对临床试验的态度量表(PACT-22)。该研究共纳入 35 个国家的 496 名参与者(89%为 IRD 成年患者,11%为患者的父母/监护人/照护者),其中大多数来自美国(69%)和英国(11%)。尽管只有 45%的参与者表示对基因治疗有很好的了解,但大多数参与者(90%)表示,如果基因治疗可用,他们很可能会接受。主要的信息来源是研究注册处(60%的参与者)和互联网(61%)。与我们最近发表的澳大利亚全国 IRD 患者调查(n=694)的数据相比,美国受访者对基因治疗结果的了解程度更高,而澳大利亚受访者表示对基因治疗的治疗效果的预期价值更高。解决有关治疗结果和经济影响的知识差距,对于确保知情同意、促进共同决策以及最终在临床上采用基因治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d793/11090820/52da5d422763/41434_2024_450_Fig1_HTML.jpg

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