Evidence map›Paper›PMID 38599660›Full record

ArticleJournal for immunotherapy of cancer2024

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

Steven T Chen, Yevgeniy R Semenov, Allireza Alloo, Daniel Q Bach, Allison Betof Warner, Amina Bougrine, Leeann Burton, Laura C Cappelli, Mariana Castells, Justine Cohen and 31 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 20 citations in OpenAlex.

  1. Sex-Biased Immunity: The Hidden Variable in Immuno-oncology.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Multidisciplinary management gaps in cancer treatment-related skin toxicities.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  8. When Checkpoint Inhibitors Break Barriers: Mechanisms and Challenges of irAEs of the Skin, Gastrointestinal Tract, and Lung.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  9. Article
  10. Perspectives on managing skin manifestations in cancer patients: a multidisciplinary mixed-method survey of oncologists and dermatologists.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  11. Review
  12. From supportive care to strategic intervention: toward a multidisciplinary approach to cutaneous adverse events in cancer treatment.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  13. Assessing Treatment Efficacy for Dermatologic Immune-Related Adverse Events: A Systematic Review.JID innovations : skin science from molecules to population health · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

41 authors at 20 institutions in 2 countries.

Steven T ChenDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0001-8844-3284
Yevgeniy R SemenovDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-7387-3094
Allireza AllooDepartment of Dermatology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York, USA.
Daniel Q BachDepartment of Dermatology, Cedars Sinai, Los Angeles, California, USA.
Allison Betof WarnerMemorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID 0000-0001-6422-2997
Amina BougrineDepartment of Dermatology, Université de Montréal, Montreal, Quebec, Canada.
Leeann BurtonBiogen Inc, Cambridge, Massachusetts, USA.
Laura C CappelliJohns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Mariana CastellsHarvard Medical School, Boston, Massachusetts, USA.
Justine CohenHarvard Medical School, Boston, Massachusetts, USA.
Anna K DewanVanderbilt University Medical Center, Nashville, Tennessee, USA.
Riley FaddenMass General Cancer Center, Boston, MA, USA.
Lauren GugginaHarvard Medical School, Boston, Massachusetts, USA.
Aparna HegdeUAB, Birmingham, Alabama, USA.ORCID 0000-0001-6616-4882
Victor HuangDepartment of Dermatology, University of California Davis, Davis, California, USA.
Douglas B JohnsonVanderbilt University Medical Center, Nashville, Tennessee, USA.
Benjamin KaffenbergerDepartment of Dermatology, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Daniela KroshinskyDepartment of Dermatology, Duke University Medical Center, Durham, North Carolina, USA.
Shawn KwatraJohns Hopkins Department of Dermatology, Baltimore, Maryland, USA.
Bernice KwongStanford University School of Medicine, Stanford, UK.
Mario E LacoutureMSKCC, New York, New York, USA.
Cecilia LaroccaHarvard Medical School, Boston, Massachusetts, USA.
Jonathan LeventhalDepartment of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA.
Alina MarkovaMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Jon McDunnProject Data Sphere ®, Morrisville, North Carolina, USA.
Meghan J MooradianMass General Cancer Center, Boston, MA, USA.ORCID 0000-0002-8289-8015
Jarushka NaidooJohns Hopkins University, The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA.ORCID 0000-0002-3470-8686
Jennifer ChoiNorthwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Vinod NambudiriHarvard Medical School, Boston, Massachusetts, USA.
Caroline A NelsonDepartment of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA.
Anisha B PatelDepartment of Dermatology, Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-5372-784X
Julia PimkinaHarvard Medical School, Boston, Massachusetts, USA.
Johnathan RineProject Data Sphere ®, Morrisville, North Carolina, USA.
Krista M RubinMass General Cancer Center, Boston, MA, USA.
Maxwell SauderDIvision of Dermatology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Sheila ShaiganyDepartment of Dermatology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York, USA.
Afreen ShariffDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Ryan J SullivanMass General Cancer Center, Boston, MA, USA.ORCID 0000-0001-5344-6645
Leyre ZubiriMass General Cancer Center, Boston, MA, USA.ORCID 0000-0003-4226-7443
Kerry L ReynoldsMass General Cancer Center, Boston, MA, USA.ORCID 0000-0002-7793-654X
Nicole R LeBoeufHarvard Medical School, Boston, Massachusetts, USA nleboeuf@bwh.harvard.edu.ORCID 0000-0002-8264-834X
Harvard University · USBrigham and Women's Hospital · USDonald & Barbara Zucker School of Medicine at Hofstra/Northwell · USMassachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USVanderbilt University Medical Center · USYale University · USBiogen (United States) · USBloomberg (United States) · USCedars-Sinai Medical Center · USDuke Medical Center · USDuke University · USJohns Hopkins University · USNorthwestern University · USNYU Langone Health · USThe Ohio State University Wexner Medical Center · USThe University of Texas MD Anderson Cancer Center · USUniversité de Montréal · CAUniversity of California, Davis · USUniversity of Toronto · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Systems Pharmacology of Therapeutic and Adverse Responses to ImmuneCheckpoint and Small Molecule DrugsU54CA225088 · NCI · HARVARD MEDICAL SCHOOL · PI SHARPE, ARLENE H. · 2018 to 2022
$10.8M
Understanding Inflammatory Arthritis due to Immune Checkpoint InhibitorsK23AR075872 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI CAPPELLI, LAURA CHRISTINE · 2019 to 2023
$779k
Predictive modeling of cutaneous immune checkpoint inhibitor toxicitiesK23AR080791 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI Yevgeniy R Semenov · 2023 to 2026
$704k
NCATS NIH HHS UL1 TR001863NCI NIH HHS P30 CA008748NCI NIH HHS U54 CA225088NIAMS NIH HHS K23 AR075872NIAMS NIH HHS K23 AR080791
6 · The paper itself

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.

Indexed as

ExanthemaOncologistsConsensusConsensus Statements as TopicHumansImmune Checkpoint InhibitorsRadioimmunotherapyImmune Checkpoint InhibitorsGuidelines as TopicImmune Checkpoint InhibitorsImmunotherapyInflammation

Identifiers

PMID38599660
PMCPMC11015215
OpenAlexW4394690662

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.