Please use this identifier to cite or link to this item: https://doi.org/10.1002/cncr.27758
Title: Phase 2 trial of linifanib (ABT-869) in patients with unresectable or metastatic hepatocellular carcinoma
Authors: Toh, H.C.
Chen, P.-J.
Carr, B.I.
Knox, J.J.
Gill, S.
Ansell, P.
McKeegan, E.M.
Dowell, B.
Pedersen, M.
Qin, Q.
Qian, J.
Scappaticci, F.A.
Ricker, J.L.
Carlson, D.M.
Yong, W.P. 
Keywords: angiogenesis
hepatocellular carcinoma (HCC)
linifanib
platelet-derived growth factor receptor (PDGFR)
sorafenib
vascular endothelial growth factor receptor (VEGFR)
Issue Date: 15-Jan-2013
Citation: Toh, H.C., Chen, P.-J., Carr, B.I., Knox, J.J., Gill, S., Ansell, P., McKeegan, E.M., Dowell, B., Pedersen, M., Qin, Q., Qian, J., Scappaticci, F.A., Ricker, J.L., Carlson, D.M., Yong, W.P. (2013-01-15). Phase 2 trial of linifanib (ABT-869) in patients with unresectable or metastatic hepatocellular carcinoma. Cancer 119 (2) : 380-387. ScholarBank@NUS Repository. https://doi.org/10.1002/cncr.27758
Abstract: Background: The efficacy and safety of linifanib (ABT-869), a selective inhibitor of vascular endothelial growth factor and platelet-derived growth factor receptor tyrosine kinases, were assessed in this phase 2, single-arm, open-label, multicenter trial. Methods: Eligible patients had unresectable or metastatic hepatocellular carcinoma and had received ≤ 1 prior systemic therapy. Patients received oral linifanib at a fasting dose of 0.25 mg/kg,. The primary endpoint was the progression-free rate at 16 weeks. Tumor response was assessed every 8 weeks. Secondary endpoints included the time to disease progression, overall survival, and objective response rate. Safety was also assessed. Results: Of the 44 patients enrolled, the majority were Asian (89%), had received no prior systemic therapy (82%), had Child-Pugh class A hepatic function (86%), and had hepatitis B virus infection (61%). The estimated progression-free rate at 16 weeks was 31.8% (34.2% for patients with Child-Pugh class A hepatic function), the estimated objective response rate was 9.1% (10.5% for patients with Child-Pugh class A hepatic function), the median time to disease progression was 3.7 months (3.7 months for patients with Child-Pugh class A hepatic function), and the median overall survival was 9.7 months (10.4 months for patients with Child-Pugh class A hepatic function). The most common linifanib-related adverse events were diarrhea (55%) and fatigue (52%). The most common linifanib-related grade 3/4 adverse events were hypertension (25%) and fatigue (14%). Serum levels of biomarkers cancer antigen (CA) 125, cytokeratin fragment (CYFRA)21.1, and protein induced by vitamin K absence or antagonist II (PIVKA) demonstrated potential as prognostic indicators of patient response or outcome. Conclusions: Single-agent linifanib was found to be clinically active in patients with advanced hepatocellular carcinoma, with an acceptable safety profile. © 2012 American Cancer Society.
Source Title: Cancer
URI: http://scholarbank.nus.edu.sg/handle/10635/116518
ISSN: 0008543X
DOI: 10.1002/cncr.27758
Appears in Collections:Staff Publications

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