Management of advanced hepatocellular carcinoma in the era of targeted therapy

被引:63
|
作者
Yau, Thomas [1 ]
Chan, Pierre [1 ]
Epstein, Richard [1 ]
Poon, Ronnie Tung Ping [2 ]
机构
[1] Queen Mary Hosp, Univ Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Queen Mary Hosp, Univ Dept Surg, Hong Kong, Hong Kong, Peoples R China
关键词
advanced hepatocellular carcinoma; bevacizumab; sorafenib; targeted therapy; ENDOTHELIAL GROWTH-FACTOR; RECEPTOR TYROSINE KINASES; RANDOMIZED PHASE-III; COMBINATION CHEMOTHERAPY; MOLECULAR PATHOGENESIS; RAF/MEK/ERK PATHWAY; ANTITUMOR-ACTIVITY; TUMOR PROGRESSION; PATIENTS PTS; EXPRESSION;
D O I
10.1111/j.1478-3231.2008.01916.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Systemic chemotherapy has had a disappointing track record in the management of advanced hepatocellular carcinoma (HCC). Single-agent doxorubicin produces a response rate of 10-15%, but without any survival benefit, and combination chemotherapy has also yielded unimpressive results. With recent advances in the knowledge of hepato-carcinogenesis, there has been encouraging development in the systemic therapy of advanced HCC patients, and particularly in the targeted therapy of advanced HCC. Among the newly identified targets, exciting results have been shown in targeting the anti-angiogenic pathway and the Raf/mitogen-activated protein kinase pathways. Bevacizumab, both as a single agent and in combination with other agents, has shown initial encouraging activity in treating advanced HCC. More recently, single-agent sorafenib, a putative multitargeted kinase inhibitor, has shown to prolong the overall survival of patients with advanced HCC in the pivotal phase III Sorafenib HCC Assessment Randomized Protocol (SHARP) and Oriental study. Currently, sorafenib is the only approved targeted therapy for patients with advanced HCC. In addition, however, promising early results have been reported for other molecular-targeted drugs including erlotinib and sunitinib. Future progress seems likely to depend on using controlled clinical trials to optimize synergistic combination treatments.
引用
收藏
页码:10 / 17
页数:8
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