Multicenter Interspecialty Consensus on Experimental Oncology Drug–Related Ocular Adverse Event Reporting

医学 分级(工程) 不利影响 重症监护医学 临床试验 入射(几何) 梅德林 多中心研究 医学物理学 内科学 肿瘤科 临床肿瘤学 分级比例尺 药物不良事件 患者安全 急诊医学 验光服务 终点测定 事件(粒子物理) 外科 事件数据
作者
Neel D. Pasricha,Stella K. Kim,Asim V. Farooq,Ethan S. Lindgren,Rongshan Yan,Gerami D. Seitzman,Matilda F. Chan,Jessica G. Shantha,Dimitra Skondra,Bennie H. Jeng,Winston Chamberlain,Kathryn Colby,Debra A. Goldstein,Lucia Sobrin,Ivana K. Kim,Kuldev Singh,Wiley Chambers,William M. Boyd,Jordyn Silverstein,Paula R. Pohlmann
出处
期刊:JAMA Ophthalmology [American Medical Association]
卷期号:144 (1): 62-62 被引量:2
标识
DOI:10.1001/jamaophthalmol.2025.3159
摘要

Importance: The current ocular Common Terminology Criteria for Adverse Events (CTCAE) mix eye signs with symptoms and lack standardized clinical photographs and experimental oncology drug dose modification recommendations. Robust reporting of ocular adverse events (AEs) is important to maintain patient safety and to guide the development of novel efficacious drugs. Objective: To develop improved ocular AE grading scales to reliably evaluate and grade ocular AEs in patients on experimental oncology drug therapy and to provide clear drug dose modification recommendations. Design, Setting, and Participants: A collaborative multicenter interspecialty working group consisting of oncologists and academic ophthalmologists from 11 academic centers in the US and ophthalmologists from the US Food and Drug Administration was assembled in February 2023 to form a consensus on new experimental oncology drug-related ocular AE grading scales. The grading scales were released in June 2023. Main Outcomes and Measures: Expert consensus on novel experimental oncology drug-related ocular AE grading scales. Results: Six experimental oncology drug-related ocular AE grading scales were developed with agreement from ophthalmologists and oncologists for use in antibody-drug conjugate clinical trials: visual acuity, eye symptoms, cornea, conjunctiva/sclera, anterior chamber, and retina/posterior segment. Conclusions and Relevance: The new experimental oncology drug-related ocular AE grading scales developed by the consensus panel were developed to be more concise, containing photographs where applicable, and to provide clear drug dose modification recommendations compared with the previous CTCAE. Use of these ocular AE grading scales may allow for more objective and consistent incidence measurements of ocular AEs throughout clinical trials and postmarketing, potentially facilitating safe testing of novel agents that may cause eye toxicity.
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