Hepatocellular carcinoma: Where there is unmet need

被引:99
作者
Bupathi, Manojkumar [1 ]
Kaseb, Ahmed [2 ]
Meric-Bernstam, Funda [1 ]
Naing, Aung [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Phase Clin Trials Program 1, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Gastrointestinal Med Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Hepatocellular carcinoma; PI3K; AKT; mTOR; Molecular targets; ENDOTHELIAL GROWTH-FACTOR; TIVANTINIB ARQ 197; RECEPTOR TYROSINE KINASE; ADVANCED SOLID TUMORS; PHASE-II TRIAL; ADULT PATIENTS; ANGIOPOIETIN-2; DISPLAYS; SIGNALING PATHWAY; POTENTIAL TARGET; SERUM-LEVELS;
D O I
10.1016/j.molonc.2015.06.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Hepatocellular carcinoma (HCC) is a complex and heterogeneous tumor most commonly associated with underlying chronic liver disease, especially hepatitis. It is a growing problem in the United States and worldwide. There are two potential ways to prevent HCC. Primary prevention which is based on vaccination or secondary prevention involving agents that slow down carcinogenesis. Several pathways have been thought to play a role in the development of HCC; specifically, those involving vascular endothelial growth factor (VEGF)-mediated angiogenesis, WNT, phosphatidylinositol 3-Idnase (PI3K)/AKT/mammalian target of rapamycin (mTOR), AMP-activated protein kinase (AMPK), and c-MET. Currently, there are only a limited number of drugs which have been proven as effective treatment options for HCC and several clinical trials are testing drugs which target aberrations in the pathways mentioned above. In this review, we discuss currently approved therapies, monotherapies and combination therapy for the treatment of HCC. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1501 / 1509
页数:9
相关论文
共 71 条
[1]
Phase II study of sorafenib in patients with advanced hepatocellular carcinoma [J].
Abou-Alfa, Ghassan K. ;
Schwartz, Lawrence ;
Ricci, Sergio ;
Amadori, Dino ;
Santoro, Armando ;
Figer, Arie ;
De Greve, Jacques ;
Douillard, Jean-Yves ;
Lathia, Chetan ;
Schwartz, Brian ;
Taylor, Ian ;
Moscovici, Marius ;
Saltz, Leonard B. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (26) :4293-4300
[2]
Secondary erythrocytosis produced by the tyrosine kinase inhibitors sunitinib and sorafenib [J].
Alexandrescu, Doru T. ;
McClure, Rebecca ;
Farzanmehr, Haleh ;
Dasanu, Constantin A. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (24) :4047-4048
[3]
[Anonymous], 2023, NCCN guidelines: treatment by cancer type
[4]
Arora Navanshu, 2011, Gastrointest Cancer Res, V4, P141
[5]
Transcriptome classification of HCC is related to gene alterations and to new therapeutic targets [J].
Boyault, Sandrine ;
Rickman, David S. ;
de Reynies, Aurelien ;
Balabaud, Charles ;
Rebouissou, Sandra ;
Jeannot, Emmanuelle ;
Herault, Aurelie ;
Saric, Jean ;
Belghiti, Jacques ;
Franco, Dominique ;
Bioulac-Sage, Paulette ;
Laurent-Puig, Pierre ;
Zucman-Rossi, Jessica .
HEPATOLOGY, 2007, 45 (01) :42-52
[6]
BRaf and MEK Inhibitors Differentially Regulate Cell Fate and Microenvironment in Human Hepatocellular Carcinoma [J].
Breunig, Christian ;
Mueller, Bernadett J. ;
Umansky, Ludmila ;
Wahl, Kristin ;
Hoffmann, Katrin ;
Lehner, Frank ;
Manns, Michael P. ;
Bantel, Heike ;
Falk, Christine S. .
CLINICAL CANCER RESEARCH, 2014, 20 (09) :2410-2423
[7]
Buitrago-Molina LE, 2012, CURR CANCER DRUG TAR, V12, P1045
[8]
Efficacy and safety of sorafenib in patients with advanced hepatocellular carcinoma according to baseline status: Subset analyses of the phase III Sorafenib Asia-Pacific trial [J].
Cheng, Ann-Lii ;
Guan, Zhongzhen ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Yang, Tsai-Sheng ;
Tak, Won Young ;
Pan, Hongming ;
Yu, Shiying ;
Xu, Jianming ;
Fang, Fang ;
Zou, Jessie ;
Lentini, Giuseppe ;
Voliotis, Dimitris ;
Kang, Yoon-Koo .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (10) :1452-1465
[9]
COXON A, 2008, P 99 ANN M AM ASS CA
[10]
Fausto N, 1991, Prog Growth Factor Res, V3, P219, DOI 10.1016/0955-2235(91)90008-R