Regional Differences in Efficacy, Safety, and Biomarkers for Second-Line Axitinib in Patients with Advanced Hepatocellular Carcinoma: From a Randomized Phase II Study
Author(s) -
Masatoshi Kudo,
YoonKoo Kang,
JoongWon Park,
Shukui Qin,
Yoshitaka Inaba,
Éric Assenat,
Yoshiko Umeyama,
María José Lechuga,
Olga Valota,
Yosuke Fujii,
JeanFrançois Martini,
James A. Williams,
Shuntaro Obi
Publication year - 2017
Publication title -
liver cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.916
H-Index - 34
eISSN - 2235-1795
pISSN - 1664-5553
DOI - 10.1159/000484620
Subject(s) - axitinib , medicine , sorafenib , hepatocellular carcinoma , oncology , placebo , subgroup analysis , proportional hazards model , ramucirumab , overall survival , meta analysis , pathology , alternative medicine
An unmet need exists for treatment of patients with advanced hepatocellular carcinoma (HCC) who progress on or are intolerant to sorafenib. A global randomized phase II trial (ClinicalTrial.gov No. NCT01210495) of axitinib, a vascular endothelial growth factor receptor 1-3 inhibitor, in combination with best supportive care (BSC) did not prolong overall survival (OS) over placebo/BSC, but showed improved progression-free survival in some patients. Subgroup analyses were conducted to identify potential predictive/prognostic factors.
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