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Cabozantinib in Patients with Advanced and Progressing Hepatocellular Carcinoma

Open access
Abou-Alfa, Ghassan K., Meyer, Tim, Cheng, Ann-Lii, El-Khoueiry, Anthony B., Rimassa, Lorenza, Ryoo, Baek-Yeol, Cicin, Irfan, Merle, Philippe, Chen, YenHsun, Park, Joong-Won, Blanc, Jean-Frederic, Bolondi, Luigi, Klümpen, Heinz-Josef, Chan, Stephen L., Zagonel, Vittorina, Pressiani, Tiziana, Ryu, Min-Hee, Venook, Alan P., Hessel, Colin, Borgman-Hagey, Anne E., Schwab, Gisela, Kelley, Robin K.·2018·New England Journal of Medicine

Abstract

BACKGROUND: Cabozantinib inhibits tyrosine kinases, including vascular endothelial growth factor receptors 1, 2, and 3, MET, and AXL, which are implicated in the progression of hepatocellular carcinoma and the development of resistance to sorafenib, the standard initial treatment for advanced disease. This randomized, double-blind, phase 3 trial evaluated cabozantinib as compared with placebo in previously treated patients with advanced hepatocellular carcinoma. METHODS: A total of 707 patients were randomly assigned in a 2:1 ratio to receive cabozantinib (60 mg once daily) or matching placebo. Eligible patients had received previous treatment with sorafenib, had disease progression after at least one systemic treatment for hepatocellular carcinoma, and may have received up to two previous systemic regimens for advanced hepatocellular carcinoma. The primary end point was overall survival. Secondary end points were progression-free survival and the objective response rate. RESULTS: At the second planned interim analysis, the trial showed significantly longer overall survival with cabozantinib than with placebo. Median overall survival was 10.2 months with cabozantinib and 8.0 months with placebo (hazard ratio for death, 0.76; 95% confidence interval [CI], 0.63 to 0.92; P=0.005). Median progression-free survival was 5.2 months with cabozantinib and 1.9 months with placebo (hazard ratio for disease progression or death, 0.44; 95% CI, 0.36 to 0.52; P<0.001), and the objective response rates were 4% and less than 1%, respectively (P=0.009). Grade 3 or 4 adverse events occurred in 68% of patients in the cabozantinib group and in 36% in the placebo group. The most common high-grade events were palmar-plantar erythrodysesthesia (17% with cabozantinib vs. 0% with placebo), hypertension (16% vs. 2%), increased aspartate aminotransferase level (12% vs. 7%), fatigue (10% vs. 4%), and diarrhea (10% vs. 2%). CONCLUSIONS: Among patients with previously treated advanced hepatocellular carcinoma, treatment with cabozantinib resulted in longer overall survival and progression-free survival than placebo. The rate of high-grade adverse events in the cabozantinib group was approximately twice that observed in the placebo group. (Funded by Exelixis; CELESTIAL ClinicalTrials.gov number, NCT01908426 .).

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Metadata

Authors
Abou-Alfa, G. K., Meyer, T., Cheng, A.-L., El-Khoueiry, A. B., Rimassa, L., Ryoo, B.-Y., Cicin, I., Merle, P., Chen, Y., Park, J.-W., Blanc, J.-F., Bolondi, L., Klümpen, H.-J., Chan, S. L., Zagonel, V., Pressiani, T., Ryu, M.-H., Venook, A. P., Hessel, C., Borgman-Hagey, A. E., Schwab, G., & Kelley, R. K.
Venue
New England Journal of Medicine
Published
2018-07-05
Volume
379
Issue
1
Pages
54-63
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2809889937
Cited by
2,344
References
30
FWCI
139.34
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Cabozantinib in Patients with Advanced and Progressing Hepatocellular Carcinoma. https://app.cochat.ai/papers/10.1056/nejmoa1717002
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Abou-Alfa, G. K., Meyer, T., Cheng, A.-L., El-Khoueiry, A. B., Rimassa, L., Ryoo, B.-Y., Cicin, I., Merle, P., Chen, Y., Park, J.-W., Blanc, J.-F., Bolondi, L., Klümpen, H.-J., Chan, S. L., Zagonel, V., Pressiani, T., Ryu, M.-H., Venook, A. P., Hessel, C., . . . Kelley, R. K. (2018). Cabozantinib in Patients with Advanced and Progressing Hepatocellular Carcinoma. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1717002

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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