Evidence map›Paper›PMID 41093625›Full record

ArticleJournal for immunotherapy of cancer2025

Consensus-based disease definitions for endocrine immune-related adverse events of immune checkpoint inhibitors.

Ling Zhu, Yee-Ming M Cheung, Cherie Chiang, Emily J Gallagher, Ole-Petter R Hamnvik, Jennifer Mammen, Zoe Quandt, Renisha Jones, Jon McDunn, Huda Al-Bahadili and 27 more

Abstract readConsensus Statement
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
  3. Article
  4. Article
  5. Article
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  7. Review
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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

37 authors.

Ling ZhuDepartment of Endocrinology, Singapore General Hospital, Singapore.ORCID http://orcid.org/0000-0001-9594-8467
Yee-Ming M CheungMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Cherie ChiangDepartment of Diabetes and Endocrinology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Emily J GallagherIcahn School of Medicine at Mount Sinai, New York, New York, USA.
Ole-Petter R HamnvikDivision of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Jennifer MammenDivision of Endocrinology, Diabetes and Metabolism, Johns Hopkins Medicine, Baltimore, Maryland, USA.
Zoe QuandtMedicine, Endocrinology, UCSF, San Francisco, California, USA.ORCID http://orcid.org/0000-0002-4568-4368
Renisha JonesProject Data Sphere LLC, Cary, North Carolina, USA.
Jon McDunnProject Data Sphere LLC, Morrisville, North Carolina, USA.
Huda Al-BahadiliDivision of Endocrinology, Metabolism and Lipid Research, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.
Trevor AngellDivision of Endocrinology and Diabetes, USC Keck School of Medicine, Los Angeles, California, USA.
Irina BancosDivision of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, Minnesota, USA.
Allison Betof WarnerStanford University School of Medicine, Stanford, California, USA.ORCID http://orcid.org/0000-0001-6422-2997
Susan BlackwellDuke Cancer Institute, Durham, North Carolina, USA.
Cassandra CalabreseDepartment of Rheumatologic and Immunologic Disease, Cleveland Clinic, Cleveland, Ohio, USA.
Tracey A ChoThe University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Michael DouganDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Michelle FerreiraJohns Hopkins Medicine, Baltimore, Maryland, USA.
Pauline FunchainStanford University School of Medicine, Stanford, California, USA.ORCID http://orcid.org/0000-0002-7568-8626
Justine HerndonDivision of Endocrinology, Diabetes, Metabolism and Nutrition, Mayo Clinic, Rochester, Minnesota, USA.
Douglas B JohnsonDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Randol KennedyDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Meenal KheterpalDepartment of Dermatology, Duke University School of Medicine, Durham, North Carolina, USA.
Michel KhouriDivision of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
Melissa G LechnerDivision of Endocrinology, Diabetes, and Metabolism, University of California Los Angeles David Geffen School of Medicine, Los Angeles, California, USA.
Annette M LimDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-0777-2279
Alina MarkovaMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Alexa MearaDivision of Oncology, The Ohio State University, Columbus, Ohio, USA.
Laura OvertonDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.
Ana Luisa PerdigotoYale University Department of Medical Oncology, New Haven, Connecticut, USA.
Nirupa SachithanandanPeter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Elad SharonDana-Farber Cancer Institute, Boston, Massachusetts, USA.
Lavinia SpainMedical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Katy TsaiHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California, USA.ORCID http://orcid.org/0000-0002-7705-1813
Mark YarchoanJohns Hopkins Medicine Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA.
Kerry L ReynoldsHarvard Medical School, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0002-7793-654X
Afreen ShariffDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina, USA afreen.shariff@duke.edu.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) are an important class of cancer treatment. Endocrine immune-related adverse events (E-irAEs) account for a significant proportion of irAEs in ICI-treated patients. Diagnosing E-irAEs accurately and timely can be challenging in the absence of clear categorization and standardization across oncology, endocrinology and other specialties. While existing guidelines provide some broad directions to diagnosis and management, they lack clarity on irAE-specific symptom evaluation and work-up, as well as assessment of severity. These limitations can then impact triage, time-sensitive management and care escalation to specialists such as oncoendocrinologists. The objective of this study was to develop consensus-based statements on disease definitions for E-irAEs.A core working group of endocrinologists with expertise in the oncoendocrinology field drafted a survey with statements outlining the general approach to E-irAEs, disease definition and management approach of six specific diagnoses: ir-thyroiditis thyrotoxic phase, ir-thyroiditis hypothyroidism, ir-Graves' disease, ir-hypophysitis, ir-adrenalitis and ir-type 1 diabetes mellitus. Severity grading tables were drafted for three disease categories-"thyroid", "pituitary and adrenal", and "diabetes mellitus". A two-round modified Delphi process, using the RAND/University of California Los Angeles (RAND/UCLA) Appropriateness Method, was employed. In this process, a 25-member voting panel consisting of endocrinologists, oncologists and other specialists and healthcare providers with experience in management of ICI-treated patients and irAEs was recruited. The panel rated anonymously on usability, accuracy, appropriateness or agreement of 41 items on a 9-point scale in Survey 1, after which a meeting was convened. Statements were modified based on voting results from Survey 1 and Meeting 1, and the process was repeated in Survey 2 and Meeting 2. At the end of this process, consensus was achieved for all statements.Our study findings address the gap in standardized nomenclature, clinical, laboratory and radiological evaluations, and management principles of E-irAEs. With consensus achieved from a panel of experts from a variety of disciplines, we anticipate that the statements can form the basis for standardization of the diagnostic process and improvement of patient care.

Indexed as

Drug-Related Side Effects and Adverse ReactionsEndocrine System DiseasesImmune Checkpoint InhibitorsNeoplasmsHumansImmune Checkpoint InhibitorsDiabetesHypophysitisImmune Checkpoint InhibitorImmune related adverse event - irAEThyroid toxicity

Identifiers

PMID41093625
PMCPMC12530408

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.