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Immune Checkpoint Inhibitor Toxicities
Julian A Marin-Acevedo1, Razvan M Chirila1, Roxana S Dronca2
1Division of General Internal Medicine, Mayo Clinic, Jacksonville, FL.
Abstract:
Immune checkpoint inhibitors are molecules that increase the endogenous immune response against tumors. They have revolutionized the field of oncology. Since their initial approval for the treatment of advanced melanoma, their use has expanded to the treatment of several other advanced cancers. Unfortunately, immune checkpoint inhibitors have also been associated with the emergence of a new subset of autoimmune-like toxicities, known as immune-related adverse events. These toxicities differ depending on the agent, malignancy, and individual susceptibilities. Although the skin and colon are most commonly involved, any organ may be affected, including the liver, lungs, kidneys, and heart. Most of these toxicities are diagnosed by excluding other secondary infectious or inflammatory causes. Corticosteroids are commonly used for treatment of moderate and severe immune-related adverse events, although additional immunosuppressive therapy may occasionally be required. The occurrence of immune-related toxicities may require discontinuation of immunotherapy, depending on the specific toxicity and its severity. In this article, we provide a focused review to familiarize practicing clinicians with this important topic given that the use of immune checkpoint inhibitors continues to increase.
Insights
Immune checkpoint inhibitors boost anti-tumor immunity but can cause immune-related adverse events. Early recognition and management are crucial for patient safety and continued cancer treatment.
Area of Science:
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) have transformed cancer therapy.
- Their use has expanded across multiple advanced cancer types.
- ICIs activate the immune system to target tumors.
Purpose of the Study:
- To review immune-related adverse events (irAEs) associated with ICIs.
- To familiarize clinicians with irAEs for increased ICI use.
- To guide management of ICI-induced toxicities.
Main Methods:
- Literature review focusing on ICI-related toxicities.
- Discussion of irAE presentation, diagnosis, and management.
- Emphasis on clinical recognition and differential diagnosis.
Main Results:
- ICIs can cause autoimmune-like toxicities (irAEs) affecting any organ.
- Skin and colon are most frequently involved.
- Diagnosis often involves excluding other causes; corticosteroids are primary treatment.
Conclusions:
- irAEs are a significant consideration in ICI therapy.
- Management requires prompt diagnosis and appropriate immunosuppression.
- Balancing immunotherapy efficacy with toxicity management is key.
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