
Vol. 27, No. 2, 2009
Free Abstract Article (References)
Article (PDF 388 KB)
Treatment and Modalities
Systemic Therapies in Hepatocellular Carcinoma
Marcus Alexander Wörns, Arndt Weinmann, Marcus Schuchmann, Peter Robert Galle
First Department of Internal Medicine, Johannes Gutenberg-University, Mainz, Germany
Address of Corresponding Author
Dig Dis 2009;27:175-188 (DOI: 10.1159/000218351)
Key Words
- Hepatocarcinogenesis
- Hepatocarcinogenesis, signaling pathways
- Hepatocellular carcinoma, systemic therapies
- Molecular hepatocarcinogenesis, overview
- Molecular targeted therapy in HCC
- Potential targets in HCC
- Systemic therapy in HCC, historical perspective
Abstract
Hepatocellular carcinoma (HCC) is one of the most common and lethal malignant tumors worldwide in the human population. Due to late diagnosis and/or advanced underlying liver cirrhosis, only limited treatment options with marginal clinical benefit are available in up to 70% of patients. During the last decades, no effective conventional cytotoxic systemic therapy was available contributing to the dismal prognosis in patients with advanced disease. However, a better knowledge of molecular hepatocarcinogenesis provides today the opportunity for targeted therapy. Positive data from the pivotal phase III SHARP trial assessing the efficacy and safety of the multikinase inhibitor sorafenib broadened the horizon for patients with advanced disease. After years of therapeutic nihilism, sorafenib was the first agent to demonstrate a statistically significant improvement in overall survival for patients with advanced HCC. This article reviews the historical perspective of systemic therapy in HCC and provides a brief overview of molecular hepatocarcinogenesis and potential targets in HCC. Most promising molecular targeted agents tested within clinical trials in advanced HCC are summarized, with a special attention to sorafenib, sunitinib, bevacizumab, and erlotinib. Copyright © 2009 S. Karger AG, Basel
Author Contacts Marcus Alexander Wörns First Department of Internal Medicine, Johannes Gutenberg University Langenbeckstrasse 1, DE–55131 Mainz (Germany) Tel. +49 6131 176 863, Fax +49 6131 176 410 E-Mail woerns@uni-mainz.de
Article Information
Disclosures of potential conflicts of interest: M.A.W., A.W. and P.R.G. have a consultant/advisory role for Bayer Health Care, Leverkusen, Germany.
Published online: June 22, 2009
Number of Print Pages : 14
Number of Figures : 0, Number of Tables : 2, Number of References : 152 |
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