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Updated: Jun 17, 2026

An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
Sorafenib
1Department of Hematology and Oncology, Freiburg University Medical Center, Hugstetterstrasse 55, 79102, Freiburg, Germany. jens.hasskarl@uniklinik-freiburg.de
Abstract:
Sorafenib (BAY 43-9006, Nexavar) is a novel oral kinase inhibitor that targets multiple tyrosine kinases in vivo and in vitro. Main targets are receptor tyrosine kinase pathways frequently deregulated in cancer such as the raf-ras pathway, vascular endothelial growth factor (VEGF) pathway, and FMS-like tyrosine kinase 3 (FLT3). Sorafenib was approved by the FDA in fast track for advanced renal cell cancer and hepatocellular cancer and shows good clinical activity in thyroid cancer. Multiple clinical trials are undertaken to further investigate the role of sorafenib alone or in combination for the treatment of various tumor entities.
Insights
Sorafenib is an oral kinase inhibitor targeting cancer pathways like raf-ras and VEGF. It is approved for advanced kidney and liver cancer, with ongoing trials for other tumor types.
Area of Science:
- Oncology
- Pharmacology
Background:
- Sorafenib is an oral kinase inhibitor targeting multiple tyrosine kinases.
- Key targets include receptor tyrosine kinase pathways deregulated in cancer, such as raf-ras, VEGF, and FLT3.
Purpose of the Study:
- To summarize the role of sorafenib in cancer treatment.
- To highlight its mechanism of action and clinical applications.
Main Methods:
- Review of in vitro and in vivo studies.
- Analysis of clinical trial data for various tumor entities.
Main Results:
- Sorafenib targets multiple receptor tyrosine kinases involved in cancer.
- FDA approval for advanced renal cell and hepatocellular cancer.
- Demonstrated clinical activity in thyroid cancer.
Conclusions:
- Sorafenib is a validated therapeutic agent for specific advanced cancers.
- Further clinical trials are investigating its efficacy in broader oncological settings.
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