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Defining D-irAEs: consensus-based disease definitions for the diagnosis of dermatologic adverse events from immune checkpoint inhibitor therapy.
Chen, Steven T; Semenov, Yevgeniy R; Alloo, Allireza; Bach, Daniel Q; Betof Warner, Allison; Bougrine, Amina; Burton, Leeann; Cappelli, Laura C; Castells, Mariana; Cohen, Justine; Dewan, Anna K; Fadden, Riley; Guggina, Lauren; Hegde, Aparna; Huang, Victor; Johnson, Douglas B; Kaffenberger, Benjamin; Kroshinsky, Daniela; Kwatra, Shawn; Kwong, Bernice; Lacouture, Mario E; Larocca, Cecilia; Leventhal, Jonathan; Markova, Alina; McDunn, Jon; Mooradian, Meghan J; Naidoo, Jarushka; Choi, Jennifer; Nambudiri, Vinod; Nelson, Caroline A; Patel, Anisha B; Pimkina, Julia; Rine, Johnathan; Rubin, Krista M; Sauder, Maxwell; Shaigany, Sheila; Shariff, Afreen; Sullivan, Ryan J; Zubiri, Leyre; Reynolds, Kerry L; LeBoeuf, Nicole R.
Affiliation
  • Chen ST; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Semenov YR; Mass General Cancer Center, Boston, MA, USA.
  • Alloo A; Harvard Medical School, Boston, Massachusetts, USA.
  • Bach DQ; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Betof Warner A; Harvard Medical School, Boston, Massachusetts, USA.
  • Bougrine A; Department of Dermatology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York, USA.
  • Burton L; Department of Dermatology, Cedars Sinai, Los Angeles, California, USA.
  • Cappelli LC; Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Castells M; Department of Dermatology, Université de Montréal, Montreal, Quebec, Canada.
  • Cohen J; Biogen Inc, Cambridge, Massachusetts, USA.
  • Dewan AK; Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Fadden R; Harvard Medical School, Boston, Massachusetts, USA.
  • Guggina L; Department of Medicine, Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Hegde A; Harvard Medical School, Boston, Massachusetts, USA.
  • Huang V; Department of Medical Oncology, Centers for Cutaneous and Melanoma Oncology, Dana-Farber Cancer Insititute, Boston, MA, USA.
  • Johnson DB; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Kaffenberger B; Mass General Cancer Center, Boston, MA, USA.
  • Kroshinsky D; Harvard Medical School, Boston, Massachusetts, USA.
  • Kwatra S; Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Kwong B; Center for Cutaneous Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Lacouture ME; UAB, Birmingham, Alabama, USA.
  • Larocca C; Department of Dermatology, University of California Davis, Davis, California, USA.
  • Leventhal J; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Markova A; Department of Dermatology, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • McDunn J; Department of Dermatology, Duke University Medical Center, Durham, North Carolina, USA.
  • Mooradian MJ; Johns Hopkins Department of Dermatology, Baltimore, Maryland, USA.
  • Naidoo J; Stanford University School of Medicine, Stanford, UK.
  • Choi J; MSKCC, New York, New York, USA.
  • Nambudiri V; NYU Langone Health, New York, New York, USA.
  • Nelson CA; Harvard Medical School, Boston, Massachusetts, USA.
  • Patel AB; Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Pimkina J; Center for Cutaneous Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Rine J; Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Rubin KM; Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Sauder M; Project Data Sphere ®, Morrisville, North Carolina, USA.
  • Shaigany S; Mass General Cancer Center, Boston, MA, USA.
  • Shariff A; Harvard Medical School, Boston, Massachusetts, USA.
  • Sullivan RJ; Johns Hopkins University, The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA.
  • Zubiri L; Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Reynolds KL; Harvard Medical School, Boston, Massachusetts, USA.
  • LeBoeuf NR; Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
J Immunother Cancer ; 12(4)2024 Apr 10.
Article in En | MEDLINE | ID: mdl-38599660
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Exanthema / Oncologists Limits: Humans Language: En Journal: J Immunother Cancer Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Exanthema / Oncologists Limits: Humans Language: En Journal: J Immunother Cancer Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom