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

delete2025-04-08
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OA
AI
E
Eileen Chang
R
Renee Liu
K
Katie Huynh
M
Meghan Berkenstock
M
M. Tariq Bhatti
J
John J. Chen
J
James Chodosh
F
Fiona Costello
L
Lauren A. Dalvin
D
Delott, Lindsey B.
M
Marc Dinkin
R
Robert A. Egan
C
Clare L. Fraser
S
Suzanne K. Freitag
S
Sapna Gangaputra
L
Lynn K. Gordon
A
Amanda C. Guidon
D
Douglas B. Johnson
N
Ninani Kombo
M
Michal Kramer
A
Andrew G. Lee
M
Michaël Levy
A
Anne-Marie Lobo-Chan
D
Dimosthenis Mantopoulos
G
George N. Papaliodis
M
Misha Pless
J
Julia S. Pimkina
K
Krista M. Rubin
H
H. Nida Sen
A
Afreen Shariff
P
Prem S. Subramanian
E
Edmund Tsui
M
Michael K. Yoon
J
Jon McDunn
J
Johnathan Rine
K
Kerry L. Reynolds
L
Lucia Sobrin *
B
Bart K. Chwalisz
DOI:10.1136/jitc-2024-011049delete
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Abstract

Abstract

En 中文
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 related adverse event - irAE
Immunotherapy
Immune Checkpoint Inhibitor

Journal

Journal for ImmunoTherapy of Cancer cover
Journal for ImmunoTherapy of Cancer
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