Cited by 123Cancer Immunotherapy and BiomarkersLung Cancer Treatments and MutationsFerroptosis and cancer prognosis

Development of thyroid dysfunction is associated with clinical response to PD-1 blockade treatment in patients with advanced non-small cell lung cancer

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Kim, Hye In, Kim, Mijin, Lee, Se-Hoon, Park, So Young, Kim, Young Nam, Kim, Hosu, Jeon, Min Ji, Kim, Tae Yong +10 more·2018·OncoImmunology

Abstract

Purpose: Drugs that blockade interaction between programmed cell-death protein 1 (PD-1) and its ligand (PD-L1) are promising. Immune-related adverse events (irAEs) might be associated with favorable clinical outcomes, and thyroid dysfunction is one of the most common irAE. We evaluated the association of thyroid dysfunction during PD-1 blockade with the treatment efficacy in patients with non-small cell lung cancer (NSCLC).Experimental Design: A total 58 patients with stage IV NSCLC treated with PD-1 blockade were enrolled. Patients were categorized into thyroid dysfunction and euthyroid groups. Overall survival (OS) and progression-free survival (PFS) of the two groups were compared. Patients, tumor, and medication factors were adjusted using Cox proportional hazard modeling. Objective response rate (RR) and durable control rate were assessed according to the severity of thyroid dysfunction.Results: OS [median 118.0 (73.0-267.0) vs. 71.0 (28.0-160.0) days, log-rank P = 0.025] and PFS [118.0 (73.0-267.0) vs. 61.0 (28.0-130.0), log-rank P = 0.014] were longer in the thyroid dysfunction group. After adjustment, thyroid dysfunction was an independent predictive factor for favorable outcome [adjusted HR = 0.11 (95% CI) 0.01-0.92 for overall death; 0.38 (0.17-0.85) for disease progression]. The severity of thyroid dysfunction was associated with durable control rate (P for trend = 0.008).Conclusions: Thyroid dysfunction during PD-1 blockade is associated with treatment response and could provide supplementary information for immune monitoring in patients with advanced NSCLC.

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Authors
Kim, H. I., Kim, M., Lee, S.-H., Park, S. Y., Kim, Y. N., Kim, H., Jeon, M. J., Kim, T. Y., Kim, S. W., Kim, W. B., Kim, S.-W., Lee, D. H., Park, K., Ahn, M.-J., Chung, J. H., Shong, Y. K., Kim, W. G., & Kim, T. H.
Affiliations
  • Samsung Medical Center (KR)
  • Asan Medical Center (KR)
  • Division of Endocrinology & Metabolism, Department of Medicine, Thyroid Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
  • Division of Oncology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
Corresponding author
  • Kim, Won Gu
  • Kim, Tae Hyuk
Venue
OncoImmunology
Published
2017-09-21
Volume
7
Issue
1
Pages
e1375642
ISSN
  • 2162-4011 (ISSN-L)
  • 2162-402X
OpenAlex
W2751281338
Cited by
123
References
26
Citations by year
2026: 8 · 2025: 6 · 2024: 16 · 2023: 13 · 2022: 20 · 2021: 23 · 2020: 20 · 2019: 13 · 2018: 4
FWCI
4.46
Type
journal article
Language
en
Open access
Locations
  • OncoImmunology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Ferroptosis and cancer prognosis
Keywords
thyroid dysfunction, anti-PD-1 therapy, immune-related adverse events, non-small cell lung cancer, immune checkpoint inhibitors, PD-L1, treatment response, overall survival, progression-free survival, immune monitoring, prognostic factors

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