Abstract | OBJECTIVE: METHODS: We searched multiple databases (PubMed, Web of Science, Cochrane, and Scopus) up to February 2020 for case reports on adrenalitis and PAI caused by ICIs. RESULTS: We identified 15 case reports on ICI-induced adrenalitis and PAI and reviewed their clinical presentation, characteristics, immunologic and imaging features, and treatment. We also developed a screening strategy for PAI in patients treated with ICIs. CONCLUSION: Given the morbidity and mortality associated with acute adrenal crisis, physicians-especially endocrinologists and oncologists-should be aware of this particular risk. PAI caused by autoimmune adrenalitis predominantly occurs in patients treated with programmed death 1 inhibitor monotherapy. PAI often coexists with other endocrinopathies and requires mineralocorticoid as well as glucocorticoid replacement. Even after withdrawal of ICIs, PAI can persist and requires lifelong replacement therapy.
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Authors | Yun Shi, Min Shen, Xuqin Zheng, Tao Yang |
Journal | Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
(Endocr Pract)
Vol. 27
Issue 2
Pg. 165-169
(Feb 2021)
ISSN: 1530-891X [Print] United States |
PMID | 33554872
(Publication Type: Journal Article, Review, Systematic Review)
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Copyright | Copyright © 2020 AACE. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Antineoplastic Agents, Immunological
- Immune Checkpoint Inhibitors
|
Topics |
- Addison Disease
(chemically induced, drug therapy)
- Adrenal Insufficiency
(chemically induced)
- Antineoplastic Agents, Immunological
(adverse effects)
- Humans
- Immune Checkpoint Inhibitors
- Neoplasms
(drug therapy)
|