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Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
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Patterns of hormonal changes in hypophysitis by immune checkpoint inhibitor
Hyunji Sang1,2, Yun Kyung Cho3,4, Sang-Hyeok Go3,4
1Department of Endocrinology and Metabolism, Kyung Hee University Hospital, Seoul, Korea.
The Korean Journal of Internal Medicine
|September 10, 2024
Summary
Immune checkpoint inhibitors (ICIs) can cause hypophysitis. This study analyzed 21 patients, finding high rates of hormone deficiencies in the hypophysitis group and a median onset of 7.7 months after ICI initiation.
Area of Science:
- Endocrinology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events, including endocrine dysfunctions.
- Immune-related hypophysitis (irH) is a significant concern, but its clinical course and characteristics require further elucidation.
Purpose of the Study:
- To analyze the clinical course and characteristics of immune-related hypophysitis (irH) in patients treated with immune checkpoint inhibitors (ICIs).
Main Methods:
- A retrospective single-center study analyzed electronic medical records of adult patients with solid tumors treated with ICIs from January 2017 to June 2021.
- Evaluated thyroid, adrenal, gonadotropin, and growth hormone function, comparing patients with and without irH.
Main Results:
- Twenty-one patients were included; 13 had irH. No significant difference in clinical characteristics was observed between groups.
- The irH group showed high deficiency rates: 76.9% for ACTH, 61.5% for gonadotropins, 23.1% for TSH, and 15.4% for GH.
- The overall incidence of irH was 0.9 per person-year, with a median onset of 7.7 months post-ICI initiation.
Conclusions:
- Findings suggest that clinical course and characteristics may aid in predicting ICI-induced irH.
- Early identification and management of irH are crucial for patient health and quality of life.

