Final efficacy and safety results and biomarker analysis of a phase 2 study of cabozantinib in Japanese patients with advanced renal cell carcinoma

• Published in: International journal of clinical oncology 2023-03, Vol.28 (3), p.416-426
• Main Authors: Nakaigawa, Noboru, Tomita, Yoshihiko, Tamada, Satoshi, Tatsugami, Katsunori, Osawa, Takahiro, Oya, Mototsugu, Kanayama, Hiroomi, Miura, Yuji, Sassa, Naoto, Nishimura, Kazuo, Nozawa, Masahiro, Masumori, Naoya, Miyoshi, Yasuhide, Kuroda, Shingo, Kimura, Akiko
• Format: Article
• Language: English
• Subjects: Biomarkers; Cancer Research; Carcinoma, Renal Cell - drug therapy; East Asian People; Growth factors; Hepatocyte growth factor; Humans; Kidney cancer; Kidney Neoplasms - drug therapy; Kinases; Medicine; Medicine & Public Health; NCT; NCT03339219; Oncology; Original; Original Article; Protein Kinase Inhibitors - therapeutic use; Protein-tyrosine kinase receptors; Receptors, Vascular Endothelial Growth Factor - antagonists & inhibitors; Renal cell carcinoma; Response rates; Safety; Surgical Oncology; Vascular endothelial growth factor; Vascular endothelial growth factor receptors
• ISSN: 1341-9625; 1437-7772; 1437-7772
• DOI: 10.1007/s10147-022-02283-w

Background Cabozantinib was established as the standard of care for the treatment of patients with renal cell carcinoma (RCC) whose disease had progressed after vascular endothelial growth factor receptor tyrosine kinase inhibitor (VEGFR-TKI) therapy in the global randomized trial METEOR. A phase 2 study was conducted to bridge the findings in METEOR to Japanese patients. Here, we report a biomarker analysis and update the efficacy and safety results of cabozantinib treatment. Methods Japanese patients with RCC who received at least one prior VEGFR-TKI were enrolled and received cabozantinib 60 mg orally once daily. The primary endpoint was objective response rate. Secondary endpoints included progression-free survival, overall survival, and safety. Exploratory analyses included the relationship between plasma protein hepatocyte growth factor (HGF) levels and treatment responses. Results In total, 35 patients were enrolled. The median treatment duration was 58.3 (range 5.1–131.4) weeks. The objective response rate was 25.7% (90% confidence interval [CI] 14.1–40.6). Kaplan–Meier estimate of median progression-free survival was 11.1 months (95% CI 7.4–18.4). The estimated progression-free survival proportion was 73.1% (95% CI 54.6–85.0) at 6 months. Median overall survival was not reached. Adverse events were consistent with those in METEOR and the safety profile was acceptable. Nonresponders to cabozantinib showed relatively higher HGF levels than responders at baseline. Conclusions Updated analyses demonstrate the long-term efficacy and safety of cabozantinib in Japanese patients with advanced RCC after at least one VEGFR-TKI therapy. Responders tended to show lower baseline HGF levels ClinicalTrials.gov Identifier: NCT03339219.