Management, biomarkers and prognosis in people developing endocrinopathies associated with immune checkpoint inhibitors
- PMID: 39779950
- DOI: 10.1038/s41574-024-01077-6
Management, biomarkers and prognosis in people developing endocrinopathies associated with immune checkpoint inhibitors
Abstract
Immune-related adverse events (irAEs), including endocrine irAEs, can occur in response to cancer immunotherapy using immune checkpoint inhibitors (ICIs). Of the endocrine irAEs, pituitary and thyroid irAEs are most frequently observed, followed by primary adrenal insufficiency, type 1 diabetes mellitus and hypoparathyroidism. Notably, pituitary irAEs and type 1 diabetes mellitus can be lethal if overlooked, potentially leading to adrenal crisis and diabetic ketoacidosis, respectively. On the other hand, pituitary and thyroid irAEs are reported to be associated with more favourable prognoses in some cancers if treated appropriately with hormone-replacement therapies. It would be useful to identify those people who are likely to develop endocrine irAEs before initiating therapy with ICIs. Anti-pituitary antibodies and thyroid autoantibodies have been identified as potential biomarkers for the development of pituitary and thyroid irAEs, respectively. This Review elaborates on the clinical characteristics and management strategies of several endocrine irAEs, using the latest research findings and guidelines published by several academic societies.
© 2025. Springer Nature Limited.
Conflict of interest statement
Competing interests: S.I. received personal fees from Ono Pharmaceutical Company, Bristol–Myers Squibb, Chugai Pharmaceutical, MSD, AstraZeneca and Merck Biopharma outside this study. T.K. has no competing interests. H.A. received grants from Ono Pharmaceutical Company, MSD, and Chugai Pharmaceutical, as well as personal fees from Ono Pharmaceutical Company, Bristol–Myers Squibb and MSD outside this study.
References
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- Corsello, S. M. et al. Endocrine side effects induced by immune checkpoint inhibitors. J. Clin. Endocrinol. Metab. 98, 1361–1375 (2013). - PubMed
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