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Thyroid Dysfunction in Lung Cancer Patients Treated with Immune Checkpoint Inhibitors (ICIs): Outcomes in a
Angelica D'Aiello1, Juan Lin2, Rasim Gucalp3
1Department of Medicine, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10467, USA.
Thyroid dysfunction is common in lung cancer patients on immune checkpoint inhibitors (ICIs). Black patients had higher rates of thyrotoxicosis, but overall thyroid dysfunction did not impact progression-free survival (PFS).
Area of Science:
- Oncology
- Endocrinology
- Immunotherapy
Background:
- Immune checkpoint inhibitors (ICIs) targeting PD-1/PD-L1 are revolutionizing lung cancer treatment.
- Thyroid dysfunction is a known immune-related adverse event (irAE) associated with ICIs.
- Understanding demographic and clinical associations with ICI-induced thyroid dysfunction is crucial for patient management.
Purpose of the Study:
- To characterize thyroid dysfunction in a multiethnic lung cancer cohort treated with ICIs.
- To investigate associations between thyroid dysfunction and baseline characteristics, including race.
- To evaluate the impact of thyroid dysfunction on progression-free survival (PFS).
Main Methods:
- Retrospective chart review of 205 lung cancer patients receiving anti-PD1 or PD-L1 agents.
- Multivariate Cox proportional hazards models to assess time to thyroid dysfunction by race.
- Log-rank test to compare PFS at 24 weeks between patients with and without thyroid dysfunction.
Main Results:
- 37.1% (76/205) of patients developed thyroid dysfunction.
- Thyroid dysfunction occurred at similar rates across racial groups (p=0.92).
- Black patients showed higher rates of thyrotoxicosis compared to White and Hispanic patients (p=0.016).
- No significant association was found between gender, concurrent chemotherapy, and thyroid dysfunction.
- Progression-free survival (PFS) was similar for patients with and without thyroid dysfunction (p=0.353).
Conclusions:
- While overall thyroid dysfunction rates were similar across races, Black race emerged as a risk factor for thyrotoxicosis.
- Immune-related thyroid dysfunction did not significantly affect PFS in this cohort.
- Further research is needed to elucidate the mechanisms underlying race-specific irAE development.
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