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Endocrine toxicity of immune checkpoint inhibitors: essential crosstalk between endocrinologists and oncologists
Frédéric Illouz1, Claire Briet1,2, Lucie Cloix3
1Department of Endocrinology, Diabetes and Nutrition, Reference Centre of Rare Thyroid Disease, Hospital of Angers, Angers Cedex 09, F-49933, France.
Abstract:
Two types of immune checkpoint inhibitors, both antibodies that target cytotoxic T-lymphocyte antigen-4 and those that target programmed cell death-protein 1, have been approved for use in melanoma, non-small-cell lung cancer, and renal cell carcinoma as first-line or second-line therapy. Their adverse events are primarily regarded as immune-related adverse events. We felt it was important to pinpoint and discuss certain preconceptions or misconceptions regarding thyroid dysfunction, hypophysitis, and diabetes induced by immune checkpoint inhibitors. We have identified areas of uncertainty and unmet requirements, including essential interaction between endocrinologists and oncologists. Five issues have been identified for discussion: (1) diagnosis of endocrine toxicity, (2) assessment of toxicity severity, (3) treatment of toxicity, (4) withdrawal or continuation of immunotherapy, (5) preventive action.
Insights
Immune checkpoint inhibitors targeting CTLA-4 and PD-1 can cause endocrine toxicities like thyroid dysfunction. This review clarifies diagnosis, severity assessment, treatment, and management strategies for these adverse events.
Area of Science:
- Immunology
- Endocrinology
- Oncology
Background:
- Immune checkpoint inhibitors (ICIs) targeting cytotoxic T-lymphocyte antigen-4 (CTLA-4) and programmed cell death-protein 1 (PD-1) are approved for melanoma, non-small-cell lung cancer, and renal cell carcinoma.
- Adverse events associated with ICIs are often immune-related, including endocrine toxicities.
Purpose of the Study:
- To address preconceptions and misconceptions surrounding endocrine dysfunctions induced by ICIs.
- To identify areas of uncertainty and unmet needs in managing ICI-related endocrine toxicities.
- To highlight the importance of collaboration between endocrinologists and oncologists.
Main Methods:
- Literature review and expert discussion.
- Identification and analysis of five key issues in managing endocrine toxicity.
Main Results:
- Five critical areas for discussion were identified: diagnosis, severity assessment, treatment of endocrine toxicity, immunotherapy withdrawal/continuation, and preventive actions.
- Emphasis on the need for clear guidelines and interdisciplinary communication.
Conclusions:
- Addressing misconceptions and establishing standardized protocols are crucial for optimal patient care.
- Enhanced collaboration between endocrinologists and oncologists is essential for managing immune-related endocrine adverse events effectively.
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