
| ID | 70813 |
| フルテキストURL | |
| 著者 |
Tamura, Keita
Department of Urology, Hamamatsu University School of Medicine
Matsushita, Yuto
Department of Urology, Hamamatsu University School of Medicine
Watanabe, Hiromitsu
Department of Urology, Hamamatsu University School of Medicine
Yanagisawa, Takafumi
Department of Urology, Jikei University School of Medicine
Mori, Keiichiro
Department of Urology, Jikei University School of Medicine
Morinaka, Hirofumi
Department of Urology, Kawasaki Medical School
Bekku, Kensuke
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Toyoda, Shingo
Department of Urology, Kindai University Faculty of Medicine
Nukaya, Takuhisa
Department of Urology, Fujita-Health University School of Medicine
Maenosono, Ryoichi
Department of Urology, Osaka Medical and Pharmaceutical University
Komura, Kazumasa
Department of Urology, Kawasaki Medical School
Araki, Motoo
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
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Fujita, Kazutoshi
Department of Urology, Kindai University Faculty of Medicine
Takahara, Kiyoshi
Department of Urology, Fujita-Health University School of Medicine
Azuma, Haruhito
Department of Urology, Osaka Medical and Pharmaceutical University
Inamoto, Teruo
Department of Urology, Hamamatsu University School of Medicine
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| 抄録 | Objectives: Sarcomatoid renal cell carcinoma (sRCC) is an aggressive histological variant associated with a poor prognosis. While immune checkpoint inhibitor (ICI)-based combinations have become the standard of care, the optimal first-line regimen, specifically dual immunotherapy (IO-IO) vs. IO plus tyrosine kinase inhibitor (IO-TKI), remains controversial. We herein examined the real-world clinical outcomes of Japanese patients with sRCC.
Methods: We conducted a retrospective multicenter study on 46 patients with advanced or metastatic sRCC receiving first-line ICI-based combination therapy between January 2018 and December 2024 (IO-IO: n = 18; IO-TKI: n = 28). In a comparative survival analysis, three favorable-risk patients in the IO-TKI group were excluded to align risk profiles, focusing on intermediate/poor-risk groups (n = 43). The primary endpoint was overall survival (OS). Results: In the entire cohort (n = 46), the objective response rate was numerically higher in the IO-TKI group (64.3%) than in the IO-IO group (50.0%) (p = 0.37). In the comparative analysis of intermediate/poor-risk patients (n = 43), progression-free survival (PFS) was slightly longer (p = 0.071), and OS was significantly longer (p = 0.016) in the IO-TKI group than in the IO-IO group. A multivariable analysis adjusted for IMDC risk categories showed favorable survival with the IO-TKI regimen (HR 0.37, p = 0.061). Conclusions: The present study indicates that first-line IO-TKI combination therapy represents a promising treatment option with a potential survival advantage over IO-IO therapy for Japanese patients with sRCC. However, due to the retrospective design and small sample size, reliably determining the comparative efficacy of these regimens remains challenging, and further validation is warranted. |
| キーワード | dual immunotherapy
immune checkpoint inhibitor
immunotherapy plus tyrosine kinase inhibitor
sarcomatoid renal cell carcinoma
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| 発行日 | 2026-05
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| 出版物タイトル |
International Journal of Urology
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| 巻 | 33巻
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| 号 | 5号
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| 出版者 | Wiley
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| 開始ページ | e70494
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| ISSN | 0919-8172
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| NCID | AA11042471
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © 2026 The Author(s).
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| 論文のバージョン | publisher
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| PubMed ID | |
| DOI | |
| 関連URL | isVersionOf https://doi.org/10.1111/iju.70494
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| ライセンス | http://creativecommons.org/licenses/by/4.0/
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| Citation | K. Tamura, Y. Matsushita, H. Watanabe, et al., “Comparative Efficacy of First-Line Immune Checkpoint Inhibitor-Based Combination Therapies in Patients With Sarcomatoid Renal Cell Carcinoma: A Japanese Multicenter Cohort Study,” International Journal of Urology33, no. 5 (2026): e70494, https://doi.org/10.1111/iju.70494.
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