ID | 119522 |
Author |
Sazuka, Tomokazu
Chiba University
Matsushita, Yuto
Hamamatsu University School of Medicine
Sato, Hiroaki
Chiba University
Osawa, Takahiro
Hokkaido University
Hinata, Nobuyuki
Hiroshima University
Hatakeyama, Shingo
Hirosaki University
Numakura, Kazuyuki
Akita University
Ueda, Kosuke
Kurume University
Kimura, Takahiro
The Jikei University School of Medicine
Takahashi, Masayuki
Tokushima University
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Tanaka, Hajime
Tokyo Medical and Dental University
Kawasaki, Yoshihide
Tohoku University
Kurahashi, Toshifumi
Hyogo Prefectural Cancer Center
Kato, Takuma
Kagawa University
Fujita, Kazutoshi
Kindai University
Miyake, Makito
Nara Medical University
Kojima, Takahiro
Aichi Cancer Center
Kitamura, Hiroshi
University of Toyama
Miyake, Hideaki
Hamamatsu University School of Medicine
Ichikawa, Tomohiko
Chiba University
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Content Type |
Journal Article
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Description | Immuno-oncology (IO) combination therapy is utilized as a first-line systemic treatment for advanced renal cell carcinoma. However, evidence supporting the use of cabozantinib after IO combination therapy is lacking. We retrospectively analyzed patients who received second-line cabozantinib after IO combination therapy using the Japanese Urological Oncology Group (JUOG) database. In total, 254 patients were enrolled in the JUOG global study, and 118 patients who received second-line cabozantinib comprised the study cohort. The objective response rate, disease control rate, second-line cabozantinib progression-free survival (PFS), and overall survival from second-line for overall were 32%, 75%, 10.5 months, and not reached, respectively, for first-line IO-IO therapy were 37%, 77%, 11.1 months, and not reached, respectively, versus 24%, 71%, 8.3 months, and not reached, respectively, for first-line IO-tyrosine kinase inhibitor therapy. In univariate and multivariate analyses, discontinuation of first-line treatment because of progressive disease and liver metastasis were independent risk factors for PFS. All-grade adverse events occurred in 72% of patients, and grade 3 or higher adverse events occurred in 28% of patients. Second line-cabozantinib after first-line IO combination therapy for advanced renal cell carcinoma was expected to be effective after either IO-IO or IO-TKI treatment and feasible in real-world practice.
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Journal Title |
Scientific Reports
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ISSN | 20452322
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Publisher | Springer Nature
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Volume | 13
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Start Page | 20629
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Published Date | 2023-11-23
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Rights | This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
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language |
eng
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Publisher
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departments |
Medical Sciences
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