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  4. A Multicenter Phase II Study of Second-Line Axitinib for Patients with Advanced Hepatocellular Carcinoma Failing First-Line Sorafenib Monotherapy
 
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A Multicenter Phase II Study of Second-Line Axitinib for Patients with Advanced Hepatocellular Carcinoma Failing First-Line Sorafenib Monotherapy

Journal
Oncologist
Date Issued
2020
Author(s)
ZHONG-ZHE LIN  
BANG-BIN CHEN  
Hung, Yi-Ping
HUANG, PO-HSIANG  
Ying-Chun Shen  
YU-YUN SHAO  
CHIH-HUNG HSU  
ANN-LII CHENG  
Lee, Rheun-Chuan
Chao, Yee
CHIUN HSU  
DOI
10.1634/theoncologist.2020-0143
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85083207398&doi=10.1634%2ftheoncologist.2020-0143&partnerID=40&md5=81d04cb9fb1a5df114f940ee1dc52a11
https://scholars.lib.ntu.edu.tw/handle/123456789/487250
Abstract
Lessons Learned: For patients with advanced hepatocellular carcinoma after failure of first-line sorafenib monotherapy, second-line axitinib provides modest efficacy with tolerable toxicity. The discrepant tumor responses and survival outcomes in trials using axitinib as salvage therapy highlight the importance of optimal patient selection with the aid of clinical biomarkers. Background: Multikinase inhibitors have been effective treatment for hepatocellular carcinoma (HCC). This multicenter phase II study explored the efficacy and safety of second-line axitinib for advanced HCC. Methods: Patients with advanced HCC and Child-Pugh A liver function, experiencing progression on first-line sorafenib monotherapy, were eligible. Axitinib 5 mg twice daily was given continuously with allowed dose escalation. Tumor assessment was performed according to RECIST version 1.1. The primary endpoint was rate of disease control. Results: From April 2011 to March 2016, 45 patients were enrolled. Thirty-seven patients (82%) tested positive for hepatitis B surface antigen. The disease control rate was 62.2%, and the response rate was 6.7%, according to RECIST criteria. Median progression-free survival (PFS) and overall survival (OS) were 2.2 months and 10.1 months, respectively. Treatment-related adverse events were compatible with previous reports of axitinib. Conclusion: Second-line axitinib has moderate activity and acceptable toxicity for patients with advanced HCC after failing the first-line sorafenib monotherapy. ? AlphaMed Press; the data published online to support this summary are the property of the authors.
SDGs

[SDGs]SDG3

Other Subjects
axitinib; hepatitis B surface antigen; sorafenib; antineoplastic agent; axitinib; carbanilamide derivative; nicotinamide; sorafenib; adult; anorexia; Article; Child Pugh score; clinical article; constipation; controlled study; drug efficacy; drug safety; dyspnea; fatigue; female; hand foot syndrome; human; hypertension; liver cell carcinoma; male; middle aged; mucosa inflammation; multicenter study; nausea; overall survival; phase 2 clinical trial; priority journal; progression free survival; proteinuria; treatment response; vomiting; clinical trial; liver tumor; treatment outcome; Antineoplastic Agents; Axitinib; Carcinoma, Hepatocellular; Humans; Liver Neoplasms; Niacinamide; Phenylurea Compounds; Sorafenib; Treatment Outcome
Publisher
Wiley-Blackwell
Type
journal article

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