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Defining D-irAEs: consensus-based disease definitions for the diagnosis of dermatologic adverse events from immune checkpoint inhibitor therapy

Authors :
Laura C Cappelli
Bernice Kwong
Jarushka Naidoo
Jonathan Leventhal
Mario E Lacouture
Meghan J Mooradian
Douglas B Johnson
Justine Cohen
Aparna Hegde
Steven T Chen
Riley Fadden
Leyre Zubiri
Shawn Kwatra
Ryan J Sullivan
Kerry L Reynolds
Allison Betof Warner
Yevgeniy R Semenov
Nicole R LeBoeuf
Krista M Rubin
Anna K Dewan
Alina Markova
Allireza Alloo
Daniel Q Bach
Amina Bougrine
Leeann Burton
Mariana Castells
Lauren Guggina
Victor Huang
Benjamin Kaffenberger
Daniela Kroshinsky
Cecilia Larocca
Jon McDunn
Jennifer Choi
Vinod Nambudiri
Caroline A Nelson
Anisha B Patel
Julia Pimkina
Johnathan Rine
Maxwell Sauder
Sheila Shaigany
Afreen Shariff
Source :
Journal for ImmunoTherapy of Cancer, Vol 12, Iss 4 (2024)
Publication Year :
2024
Publisher :
BMJ Publishing Group, 2024.

Abstract

With an increasing number of patients eligible for immune checkpoint inhibitors, the incidence of immune-related adverse events (irAEs) is on the rise. Dermatologic immune-related adverse events (D-irAEs) are the most common and earliest to manifest, often with important downstream consequences for the patient. Current guidelines lack clarity in terms of diagnostic criteria for D-irAEs. The goal of this project is to better define D-irAE for the purposes of identification, diagnosis, and future study of this important group of diseases.The objectives of this project were to develop consensus guidance for an approach to D-irAEs including disease definitions and severity grading. Knowing that consensus among oncologists, dermatologists, and irAE subspecialists would be critical for usability, we formed a Dermatologic irAE Disease Definition Panel. The panel was composed of 34 experts, including oncologists, dermatologists, a rheumatologist, and an allergist/immunologist from 22 institutions across the USA and internationally. A modified Delphi consensus process was used, with two rounds of anonymous ratings by panelists and two virtual meetings to discuss areas of controversy. Panelists rated content for usability, appropriateness, and accuracy on 9-point scales in electronic surveys and provided free text comments. A working group aggregated survey responses and incorporated them into revised definitions. Consensus was based on numeric ratings using the RAND/UCLA Appropriateness Method with prespecified definitions.Following revisions based on panelist feedback, all items received consensus in the second round of ratings. Consensus definitions were achieved for 10 core D-irAE diagnoses: ICI-vitiligo, ICI-lichen planus, ICI-psoriasis, ICI-exanthem, ICI-bullous pemphigoid, ICI-Grover’s, ICI-eczematous, ICI-eruptive atypical squamous proliferation, ICI-pruritus without rash, and ICI-erosive mucocutaneous. A standard evaluation for D-irAE was also found to reach consensus, with disease-specific exceptions detailed when necessary. Each disorder’s description includes further details on disease subtypes, symptoms, supportive exam findings, and three levels of diagnostic certainty (definite, probable, and possible).These consensus-driven disease definitions standardize D-irAE classification in a useable framework for multiple disciplines and will be the foundation for future work. Given consensus on their accuracy and usability from a representative panel group, we anticipate that they can be used broadly across clinical and research settings.

Details

Language :
English
ISSN :
20511426
Volume :
12
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Journal for ImmunoTherapy of Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.0f9ad47d419c4ad4b3131ec90c49be9f
Document Type :
article
Full Text :
https://doi.org/10.1136/jitc-2023-007675