Literature DB >> 20707757

Molecular targeted therapy of advanced hepatocellular carcinoma beyond sorafenib.

Thomas Yau1, Roberta Pang, Pierre Chan, Ronnie T Poon.   

Abstract

IMPORTANCE OF THE FIELD: With 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 REVIEW: This 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 GAIN: After 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 MESSAGE: The 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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Year:  2010        PMID: 20707757     DOI: 10.1517/14656561003724705

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  5 in total

Review 1.  The two faces of FBW7 in cancer drug resistance.

Authors:  Zhiwei Wang; Hidefumi Fukushima; Daming Gao; Hiroyuki Inuzuka; Lixin Wan; Alan W Lau; Pengda Liu; Wenyi Wei
Journal:  Bioessays       Date:  2011-08-30       Impact factor: 4.345

2.  Novel antiangiogenic therapies against advanced hepatocellular carcinoma (HCC).

Authors:  R A Pazo-Cid; M Lanzuela; G Esquerdo; J L Pérez-Gracia; A Antón; G Amigo; J Martínez Trufero; A L García-Otín; P Martín-Duque
Journal:  Clin Transl Oncol       Date:  2012-07-18       Impact factor: 3.405

3.  Endoplasmic reticulum stress promotes autophagy and apoptosis and reverses chemoresistance in human ovarian cancer cells.

Authors:  Jin-Long Hu; Xin-Long Hu; Ai-Ye Guo; Chao-Jie Wang; Yi-Yang Wen; Shun-Dong Cang
Journal:  Oncotarget       Date:  2017-07-25

4.  Mistletoe extract Fraxini inhibits the proliferation of liver cancer by down-regulating c-Myc expression.

Authors:  Peiying Yang; Yan Jiang; Yong Pan; Xiaoping Ding; Patrea Rhea; Jibin Ding; David H Hawke; Dean Felsher; Goutham Narla; Zhimin Lu; Richard T Lee
Journal:  Sci Rep       Date:  2019-04-23       Impact factor: 4.379

5.  A (90)Y-labelled anti-ROBO1 monoclonal antibody exhibits antitumour activity against hepatocellular carcinoma xenografts during ROBO1-targeted radioimmunotherapy.

Authors:  Kentaro Fujiwara; Keitaro Koyama; Kosuke Suga; Masako Ikemura; Yasutaka Saito; Akihiro Hino; Hiroko Iwanari; Osamu Kusano-Arai; Kenichi Mitsui; Hiroyuki Kasahara; Masashi Fukayama; Tatsuhiko Kodama; Takao Hamakubo; Toshimitsu Momose
Journal:  EJNMMI Res       Date:  2014-06-01       Impact factor: 3.138

  5 in total

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