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Risk Factors for Cutaneous Immune-Related Adverse Events in the Japanese Population: A Retrospective Single-Center
Tomoya Watanabe1, Kohei Yamakawa1, Miyu Kobayashi2
1Department of Environmental Immuno-Dermatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Combination immunotherapy increases the risk of skin immune-related adverse events (irAEs). Higher eosinophil counts and melanoma also elevate this risk. Female sex and elevated monocyte counts are linked to severe skin irAEs.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Immune checkpoint inhibitors (ICIs) can cause immune-related adverse events (irAEs).
- Cutaneous irAEs are common and occur early, but risk factors are unclear.
- Understanding these factors is crucial for patient management.
Purpose of the Study:
- To identify risk factors for the development and severity of cutaneous irAEs in patients receiving ICIs.
- To analyze the association between specific ICI therapies and cutaneous irAEs.
- To investigate demographic and hematological factors influencing cutaneous irAE risk.
Main Methods:
- Retrospective analysis of 1224 Japanese patients treated with ICIs from 2014-2024.
- Multivariable logistic regression analysis to identify risk factors.
- Evaluation of ICI type, baseline eosinophil and monocyte counts, sex, and cancer type (melanoma).
Main Results:
- 10.9% of patients experienced cutaneous irAEs; 1.5% had grade 4 events.
- Combination anti-PD-1 and anti-CTLA-4 therapy significantly increased cutaneous irAE risk compared to monotherapy.
- Higher baseline eosinophil counts and melanoma diagnosis were associated with increased cutaneous irAE risk.
- Female sex and high baseline monocyte counts were risk factors for severe (grade 4) cutaneous irAEs.
Conclusions:
- Combination ICI therapy, elevated eosinophils, and melanoma are risk factors for developing cutaneous irAEs.
- Female sex and elevated monocytes are associated with severe cutaneous irAEs.
- These findings aid in predicting and managing ICI-induced skin toxicities.
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