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Kawada, Tatsushi Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Katayama, Satoshi Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yanagisawa, Takafumi Department of Urology, The Jikei University School of Medicine
Mori, Keiichiro Department of Urology, The Jikei University School of Medicine
Fukuokaya, Wataru Department of Urology, The Jikei University School of Medicine
Komura, Kazumasa Department of Urology, Osaka Medical and Pharmaceutical University
Tsujino, Takuya Department of Urology, Osaka Medical and Pharmaceutical University
Maenosono, Ryoichi Department of Urology, Osaka Medical and Pharmaceutical University
Takahara, Kiyoshi Department of Urology, Fujita Health University School of Medicine
Nukaya, Takuhisa Department of Urology, Fujita Health University School of Medicine
Inoki, Lan Department of Urology, Kindai University Faculty of Medicine
Toyoda, Shingo Department of Urology, Kindai University Faculty of Medicine
Hashimoto, Takeshi Department of Urology, Tokyo Medical University
Hirasawa, Yosuke Department of Urology, Tokyo Medical University
Edamura, Kohei Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kobayashi, Tomoko Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Bekku, Kensuke Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Nishimura, Shingo Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Iwata, Takehiro Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID
Sadahira, Takuya Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID researchmap
Tominaga, Yusuke Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yamanoi, Tomoaki Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yoshinaga, Kasumi Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Tsuboi, Kazuma Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kobayashi, Yasuyuki Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID
Takamoto, Atsushi Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kurose, Kyohei Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kimura, Takahiro Department of Urology, The Jikei University School of Medicine
Azuma, Haruhito Department of Urology, Osaka Medical and Pharmaceutical University
Shiroki, Ryoichi Department of Urology, Fujita Health University School of Medicine
Fujita, Kazutoshi Department of Urology, Kindai University Faculty of Medicine
Ohno, Yoshio Department of Urology, Tokyo Medical University
Araki, Motoo Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID publons researchmap
Abstract
Immune checkpoint inhibitors (ICIs) are a key component of first-line treatment for metastatic renal cell carcinoma (mRCC). However, predicting treatment-related adverse events (TRAEs) remains challenging. This study investigated the utility of eosinophil-related biomarkers as predictors of Common Terminology Criteria for Adverse Events grade ≥ 3 TRAEs in mRCC patients undergoing ICI combination therapy. In this retrospective analysis across 21 hospitals in Japan, we examined 180 patients treated with ICI/ICI therapy and 216 patients treated with ICI/tyrosine kinase inhibitor (TKI) therapy. Grade ≥ 3 TRAEs occurred in 39.4% and 31.9% of patients in the ICI/ICI and ICI/TKI groups, respectively. An elevated eosinophil proportion of ≥ 2.0% (odds ratio [OR]: 2.36; 95% CI [confidence interval] 1.23–4.54, p = 0.01) and a low neutrophil/eosinophil ratio (NER) of ≤ 40.0 (OR: 2.78, 95% CI 1.39–5.53, p = 0.004) were significant predictors of severe TRAEs in the ICI/ICI group. However, no significant associations were found in the ICI/TKI group. These findings may help identify patients who suffer from grade ≥ 3 TRAEs and help determine individualized treatment strategies in patients with mRCC.
Keywords
Renal cell carcinoma
Immune checkpoint inhibitor
ICI
Eosinophil
Immune-related adverse event
Treatment-related adverse event
Published Date
2025-07-25
Publication Title
Scientific Reports
Volume
volume15
Issue
issue1
Publisher
Springer Science and Business Media LLC
Start Page
27163
ISSN
2045-2322
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2025
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DOI
Related Url
isVersionOf https://doi.org/10.1038/s41598-025-08767-9
License
http://creativecommons.org/licenses/by-nc-nd/4.0/
Citation
Kawada, T., Katayama, S., Yanagisawa, T. et al. Eosinophils as a predictive marker of treatment-related adverse events in mRCC patients treated with first-line immune-checkpoint inhibitor combination therapy. Sci Rep 15, 27163 (2025). https://doi.org/10.1038/s41598-025-08767-9