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

Steven T. Chen(Harvard University), Yevgeniy R. Semenov(Harvard University), Allireza Alloo(Donald & Barbara Zucker School of Medicine at Hofstra/Northwell), Daniel Q. Bach(Cedars-Sinai Medical Center), Allison Betof Warner(Memorial Sloan Kettering Cancer Center), Amina Bougrine(Université de Montréal), Leeann B Burton(Biogen (United States)), Laura C. Cappelli(Johns Hopkins University), Mariana Castells(Brigham and Women's Hospital), Justine V. Cohen(Harvard University), Anna K. Dewan(Vanderbilt University Medical Center), Riley Fadden(Massachusetts General Hospital), Lauren Guggina(Brigham and Women's Hospital), Aparna Hegde, Victor Huang(University of California, Davis), Douglas B. Johnson(Vanderbilt University Medical Center), Benjamin H. Kaffenberger(The Ohio State University Wexner Medical Center), Daniela Kroshinsky(Duke Medical Center), Shawn G. Kwatra, Bernice Y. Kwong, Mario E. Lacouture(NYU Langone Health), Cecilia Larocca(Brigham and Women's Hospital), Jonathan S. Leventhal(Yale University), Alina Markova(Memorial Sloan Kettering Cancer Center), Jon McDunn, Meghan J. Mooradian(Harvard University), Jarushka Naidoo(Bloomberg (United States)), Jennifer N. Choi(Northwestern University), Vinod E. Nambudiri(Brigham and Women's Hospital), Caroline A. Nelson(Yale University), Anisha B. Patel(The University of Texas MD Anderson Cancer Center), Julia Pimkina(Harvard University), Johnathan Rine, Krista M. Rubin(Massachusetts General Hospital), Maxwell Sauder(University of Toronto), Sheila Shaigany(Donald & Barbara Zucker School of Medicine at Hofstra/Northwell), Afreen Shariff(Duke University), Ryan J. Sullivan(Harvard University), Leyre Zubiri(Harvard University), Kerry L. Reynolds(Harvard University), Nicole R. LeBoeuf(Brigham and Women's Hospital)
Journal for ImmunoTherapy of Cancer
April 1, 2024
Cited by 25Open Access
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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.


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