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. 2025 Apr 8;13(4):e011049.
doi: 10.1136/jitc-2024-011049.

Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitors

Affiliations

Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitors

Eileen L Chang et al. J Immunother Cancer. .

Abstract

Ophthalmic immune-related adverse events (Eye-irAEs) from immune checkpoint inhibitors can cause visual morbidity. The absence of standardized definitions for Eye-irAEs not only impedes the development of evidence-based treatments but also progress in translational research. The objective of this study was to develop consensus guidance for an approach to Eye-irAEs.Four ophthalmic physicians (uveitis specialists and neuro-ophthalmologists) drafted Eye-irAE consensus guidance and definitions, which were reviewed by the multidisciplinary Eye-irAE definition panel. The panel was divided into Group A (Neuro-ophthalmology/Orbital Disease) and Group B (Uveitis/Ocular Surface Disease). A modified Delphi consensus process was used, with two rounds of anonymous ratings by panelists and two meetings to discuss areas of controversy. For each disorder, five diagnostic components were evaluated: symptoms, examination findings, laboratory studies/imaging findings, diagnostic criteria, and treatment. Panelists rated content for usability, appropriateness and accuracy on 9-point scales in electronic surveys and provided free-text comments. Aggregated survey responses were incorporated into revised definitions. Consensus was based on numeric ratings using the RAND Corporation/ University of California Los Angeles Health Services Utilization Study (RAND/UCLA) Appropriateness Method with prespecified definitions.29 panelists from 25 academic medical centers voted on 114 rating scales (66 neuro-ophthalmic/orbital disease components, 48 uveitis/ocular surface disease components); of these, 86.3% (57/66) in Group A and 89.6% (43/48) in Group B reached first-round consensus. After revisions, all items except 6.1% (4/66) in Group A and 1.6% (1/60) in Group B received second-round consensus. Consensus definitions were achieved for 10/11 neuro-ophthalmic/orbital disorders: optic neuritis, inflammatory optic disc edema, arteritic ischemic optic neuropathy, optic perineuritis, orbital inflammation, thyroid eye disease-like orbital inflammation, cavernous sinus syndrome, oculomotor mononeuritis, trochlear mononeuritis, and abducens mononeuritis. Consensus definitions were achieved for 9/10 uveitis/ocular surface disorders: anterior uveitis, intermediate uveitis, posterior uveitis, panuveitis, Vogt-Koyanagi-Harada-like syndrome, sarcoidosis-like syndrome, acute macular neuroretinopathy, dry eye disease, and scleritis.These disease definitions establish a standardized classification for Eye-irAE, highlighting differences between irAEs and other inflammatory disorders. Importantly, diagnostic certainty does not always align directly with the need to treat as an Eye-irAE. Given the consensus from this representative panel group, it is anticipated the definitions will be used broadly across clinical and research settings.

Keywords: Immune Checkpoint Inhibitor; Immune related adverse event - irAE; Immunotherapy.

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Conflict of interest statement

Competing interests: FC is on the advisory board of Healio Live, Horizon Therapeutics, Sanofi, and Alexion. LAD is a consultant for IDEAYA Biosciences and has funding from the CTSA Grant Number KL2 TR002379 from the National Center for Advancing Translational Science. SKF is a consultant/advisory board member for Amgen, Sling, Viridian, Immunovant, Poriferous, Lassen, Merida/Third Rock, WL Gore, Kriya, Medtronic, Janssen. ACG receives grant support from MGNet Rare Disease Network for the ADAPT teleMG study on telemedicine in MG, Explore MG2 natural history study (NIH Rare Disease Clinical Research Network Consortium supported by U54 NS115054), Wearable Sensor and Digital Technologies for Quantitative Assessment and Remote Monitoring of Symptoms in Myasthenia Gravis (Project Number1R44NS122672), and Project Data Sphere and the Dysimmune Disease Foundation for work in neurologic immune-related adverse events. She is also on the medical advisory boards for UCB, Alexion, Argenx, Regeneron. DBJ has served on advisory boards or as a consultant for AstraZeneca, BMS, The Jackson Laboratory, Merck, Mosaic ImmunoEngineering, Novartis, Pfizer, Targovax, and Teiko, and has received research funding from BMS and Incyte, and has patents pending for use of MHC-II as a biomarker for immune checkpoint inhibitor response, and abatacept as treatment for immune-related adverse events. AGL is a consultant for Amgen, Alexion, Viridian, AstraZeneca, Bristol Myers Squibb, Stoke, NFL, NASA, and US DOJ. HNS is an employee of Sanofi Pharmaceuticals R&D. AS is a speaker for Novartis and Merck and a consultant for Merck and BMS. The remaining authors have no reported competing interests.

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