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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
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
Content Type
Journal Article
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.
Journal Title
Scientific Reports
ISSN
20452322
Publisher
Springer Nature
Volume
13
Start Page
20629
Published Date
2023-11-23
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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departments
Medical Sciences