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[Endocrine consequences of immune checkpoint inhibitors]
A S Chachati1, I Potorac1, P Petrossians1
1Service d'Endocrinologie, CHU Liège, Belgique.
Abstract:
Immune checkpoints inhibitors have fundamentally changed the management of oncologic patients. These treatments consist of monoclonal antibodies directed against CTLA-4 (cytotoxic T-lymphocyte antigen 4), PD-1 (programmed cell death protein-1) and PD-L1 (one of its ligands). By blocking these receptors or ligands, the antibodies reverse the immune tolerance induced by the cancerous cell on the T-lymphocyte and favour lymphocytic reactivation and anti-tumor activity. Immune tolerance to auto-antigens is maintained with the help of these checkpoints. Targeting them can lead to auto-immune side effects. These latter mostly impact the cutaneous and digestive system, but the endocrine glands are not spared. In this article, we provide monitoring and treatment algorithms for these endocrine immune side effects. An early diagnosis followed by the appropriate treatment would reduce their negative impact on the oncologic care.
Insights
Immune checkpoint inhibitors, like those targeting CTLA-4, PD-1, and PD-L1, can cause immune-related side effects affecting endocrine glands. Early diagnosis and treatment are crucial for managing these side effects in cancer patients.
Area of Science:
- Oncology
- Immunology
- Endocrinology
Background:
- Immune checkpoint inhibitors (ICIs) targeting CTLA-4, PD-1, and PD-L1 have revolutionized cancer treatment.
- ICIs restore anti-tumor T-cell activity by blocking immune tolerance mechanisms.
- While effective, ICIs can disrupt the natural immune tolerance to auto-antigens, leading to immune-related adverse events (irAEs).
Purpose of the Study:
- To outline monitoring and treatment strategies for endocrine immune side effects caused by ICIs.
- To emphasize the importance of early detection and intervention for managing irAEs.
- To provide clinicians with practical algorithms for addressing endocrine irAEs in cancer patients.
Main Methods:
- Review of current literature on ICI-induced endocrine irAEs.
- Development of clinical algorithms for monitoring and managing endocrine irAEs.
- Analysis of common endocrine glands affected by ICIs.
Main Results:
- Endocrine glands are frequently affected by ICI therapy, alongside cutaneous and digestive systems.
- Specific monitoring protocols and treatment algorithms are proposed for endocrine irAEs.
- Timely management of endocrine irAEs can mitigate negative impacts on cancer care.
Conclusions:
- ICI therapy necessitates vigilant monitoring for endocrine irAEs.
- Implementing structured monitoring and treatment algorithms is essential for optimal patient outcomes.
- Proactive management of endocrine irAEs supports the successful continuation of oncologic care.
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