• Expert Opin Pharmacother · Sep 2010

    Review

    Molecular targeted therapy of advanced hepatocellular carcinoma beyond sorafenib.

    • Thomas Yau, Roberta Pang, Pierre Chan, and Ronnie T Poon.
    • The University of Hong Kong, Queen Mary Hospital, Department of Medicine, Hong Kong.
    • Expert Opin Pharmacother. 2010 Sep 1;11(13):2187-98.

    Importance Of The FieldWith the recent advances in the knowledge of molecular biology of hepatocellular carcinoma (HCC), there have been encouraging developments in targeted therapy for advanced HCC.Areas Covered In This ReviewThis review discusses the development of targeted therapy for advanced HCC patient since 2006. Among the newly identified targets, promising results have been shown in targeting the anti-angiogenic pathway. Pure anti-angiogenic agents such as bevacizumab and PTK 787 demonstrate modest activity in treating patients with advanced HCC. Sorafenib, a multi-targeted tyrosine kinase inhibitor with both anti-angiogenic and anti-proliferative effects, has been shown to prolong the overall survival of patients with advanced HCC in two Phase III randomized trials. Like sorafenib, other anti-angiogenic multi-targeted tyrosine kinase inhibitors, such as sunitinib, pazopanib, brivanib and linifanib, also show promising activity in various stages of clinical trials. Other on-going early-phase studies are exploring the activities of drugs targeting novel pathways, such as PI3K/AKT/m TOR, hepatocyte growth factor/mesenchymal epithelial transition factor and insulin-like growth factor.What The Reader Will GainAfter reading this review, the reader should have an in-depth understanding of the latest developments in the molecular targeted therapy of advanced HCC.Take Home MessageThe development of sorafenib in the treatment of advanced HCC proves the concept that molecular targeted therapies, especially anti-angiogenic agents, play a pivotal role in the treatment of this otherwise chemoresistant neoplasm. Future progress depends on further unraveling more molecular mechanisms of HCC for therapeutic intervention.

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