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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 ORCID Kaken ID publons researchmap
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
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
発行日
2026-05
出版物タイトル
International Journal of Urology
巻
33巻
号
5号
出版者
Wiley
開始ページ
e70494
ISSN
0919-8172
NCID
AA11042471
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2026 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
関連URL
isVersionOf https://doi.org/10.1111/iju.70494
ライセンス
http://creativecommons.org/licenses/by/4.0/
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.