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Sicca induced by immune checkpoint inhibitors
Rakiba Belkhir1, Marjolaine Gosset2, Antoine Rousseau3
1Rheumatology Department, FHU CARE, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Bicêtre, Le Kremlin-Bicêtre, Paris, France.
Summary
Immune checkpoint inhibitors (ICIs) can cause sicca syndrome, affecting 5-24% of patients. Early detection and management, distinct from Sjögren disease, are crucial for improving patient quality of life.
Area of Science:
- Oncology
- Immunology
- Rheumatology
Background:
- Immune checkpoint inhibitors (ICIs) have transformed cancer therapy.
- Immune-related adverse events (irAEs) are common with ICIs, including sicca syndrome (ocular/oral dryness).
- ICI-induced sicca syndrome is under-recognized and impacts patient quality of life.
Purpose of the Study:
- Review prevalence, clinical features, and management of ICI-induced sicca syndrome.
- Differentiate ICI-induced sicca from Sjögren disease (SjD).
- Emphasize early detection and treatment strategies.
Main Methods:
- Literature review focusing on ICI-induced sicca syndrome.
- Analysis of prevalence, clinical presentation, and pathophysiology.
- Evaluation of current and proposed management strategies.
Main Results:
- ICI-induced sicca affects an estimated 5-24% of patients.
- Pathophysiology involves T-lymphocyte infiltration of salivary glands, differing from SjD.
- Management includes symptomatic relief and corticosteroids.
Conclusions:
- ICI-induced sicca is a significant irAE requiring attention.
- Further research needed on frequency, screening, early treatments, and long-term outcomes.
- Multidisciplinary collaboration is essential for guideline development and improved patient care.
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