Int. Journal of Clinical Pharmacology and Therapeutics, Volume 62 (2024) - February (69 - 76)

Effect of pre-treatment with EGFR-TKIs on immune checkpoint inhibitor-associated interstitial lung disease in lung cancer patients: Analysis using a Japanese claims database
Naoto Okada1, 2, Hirofumi Hamano3, 4, Kenta Yagi5, Takahiro Niimura5, Fuka Aizawa2, Mitsuhiro Goda2, 3, Yoshito Zamami3, 4, Takashi Kitahara1, 6, Keisuke Ishizawa2, 3, 5
1 Pharmacy Department, Yamaguchi University Hospital, Yamaguchi, 2 Department of Pharmacy, 3 Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, 4 Department of Pharmacy, Okayama University Hospital, Okayama, 5 Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, and 6 Clinical Pharmacology, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan

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DOI 10.5414/CP204491

Abstract

Background: Immune checkpoint inhibitors (ICI) and epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKI) are key drugs for the treatment of EGFR mutation-positive lung cancer. While previous studies reported that the concomitant use of these drugs increases the risk of interstitial lung disease (ILD), the impact of sequential treatment on ILD risk is unknown. This study aimed to analyze the impact of EGFR-TKI pre-treatment on the risk of developing ILD after subsequent ICI administration.
Materials and methods: We conducted a retrospective study using a Japanese health insurance claims database. ILD-naive lung cancer patients who had first ICI administration during the screening period from July 2014 to February 2019 were selected. Patients who had ILD within 1 year of receiving the first ICI dose were included in the ILD group. Multivariate logistic regression analysis was conducted to evaluate the effect of pre-treatment with EGFR-TKI on the development of ICI-associated ILD.
Results: A total of 353 patients were included, of which 61 were included in the ILD group. The median time to onset of ILD after ICI administration was 3 months. Multivariate logistic regression analysis revealed that pre-treatment with EGFR-TKI was not associated with ICI-associated ILD (odds ratio: 0.26, 95% confidence interval: 0.033 – 2.01).
Conclusion: Although further analyses are required to confirm our findings, this study indicated that pre-treatment with EGFR-TKI might not increase the ILD risk after ICI treatment.


Author Details

Authors

Departments

  • 1 Pharmacy Department, Yamaguchi University Hospital, Yamaguchi,
  • 2 Department of Pharmacy,
  • 3 Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima,
  • 4 Department of Pharmacy, Okayama University Hospital, Okayama,
  • 5 Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, and
  • 6 Clinical Pharmacology, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan

Address

Naoto Okada, PhD
Pharmacy Department, Yamaguchi University Hospital
1-1-1 Minamikogushi, Ube
Yamaguchi, 775-8505, Japan
Email: [email protected]

Citation

Naoto Okada, Hirofumi Hamano, Kenta Yagi, Takahiro Niimura, Fuka Aizawa, Mitsuhiro Goda, Yoshito Zamami, Takashi Kitahara, Keisuke Ishizawa.Effect of pre-treatment with EGFR-TKIs on immune checkpoint inhibitor-associated interstitial lung disease in lung cancer patients: Analysis using a Japanese claims database. Int J Clin Pharmacol Ther. 2024; 62: 69-76. doi: 10.5414/CP204491. Pubmed: https://pubmed.ncbi.nlm.nih.gov/37969096/; PMID: 37969096.

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