ID | 69044 |
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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
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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
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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.
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Keywords | Renal cell carcinoma
Immune checkpoint inhibitor
ICI
Eosinophil
Immune-related adverse event
Treatment-related adverse event
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Published Date | 2025-07-25
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Publication Title |
Scientific Reports
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Volume | volume15
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Issue | issue1
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Publisher | Springer Science and Business Media LLC
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Start Page | 27163
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ISSN | 2045-2322
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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Copyright Holders | © The Author(s) 2025
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File Version | publisher
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PubMed ID | |
DOI | |
Related Url | isVersionOf https://doi.org/10.1038/s41598-025-08767-9
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License | http://creativecommons.org/licenses/by-nc-nd/4.0/
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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
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