Please use this identifier to cite or link to this item: https://doi.org/10.1002/cncr.27758
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dc.titlePhase 2 trial of linifanib (ABT-869) in patients with unresectable or metastatic hepatocellular carcinoma
dc.contributor.authorToh, H.C.
dc.contributor.authorChen, P.-J.
dc.contributor.authorCarr, B.I.
dc.contributor.authorKnox, J.J.
dc.contributor.authorGill, S.
dc.contributor.authorAnsell, P.
dc.contributor.authorMcKeegan, E.M.
dc.contributor.authorDowell, B.
dc.contributor.authorPedersen, M.
dc.contributor.authorQin, Q.
dc.contributor.authorQian, J.
dc.contributor.authorScappaticci, F.A.
dc.contributor.authorRicker, J.L.
dc.contributor.authorCarlson, D.M.
dc.contributor.authorYong, W.P.
dc.date.accessioned2014-12-12T07:50:50Z
dc.date.available2014-12-12T07:50:50Z
dc.date.issued2013-01-15
dc.identifier.citationToh, 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
dc.identifier.issn0008543X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/116518
dc.description.abstractBackground: 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/cncr.27758
dc.sourceScopus
dc.subjectangiogenesis
dc.subjecthepatocellular carcinoma (HCC)
dc.subjectlinifanib
dc.subjectplatelet-derived growth factor receptor (PDGFR)
dc.subjectsorafenib
dc.subjectvascular endothelial growth factor receptor (VEGFR)
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1002/cncr.27758
dc.description.sourcetitleCancer
dc.description.volume119
dc.description.issue2
dc.description.page380-387
dc.description.codenCANCA
dc.identifier.isiut000313365500019
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