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Ongoing Clinical Trials

Phase II Trial of Sorafenib with Capecitabine and Oxaliplatin in Advanced Hepatocellular Carcinoma

Official Title Phase II Study of Sorafenib with Capecitabine and Oxaliplatin in Advanced Hepatocellular Carcinoma
Countries Hong Kong and Singapore
Study Arm Single arm: All patients will receive Sorafenib with Capecitabine and Oxaliplatin
Description

HCC is an aggressive, largely chemo-resistant cancer with a poor prognosis, currently there is no effective systemic chemotherapy for HCC. Vascular endothelial growth factor (VEGF), a potent stimulator of angiogenesis, is overexpressed in HCC and thought to contribute to tumor development. Oxaliplatin in combination with other chemotherapies or biologic agents have been shown to be an effective and safe treatment in advanced HCC patients. Sorafenib, an oral multi-kinase inhibitor, blocks tumor cell proliferation by targeting multiple growth factor pathways and also exerts an anti-angiogenic effect via inhibition of VEGF.

This study aims to evaluate combination of Sorafenib and a combining chemotherapy (Capecitabine and Oxaliplatin) cytotoxic drug to achieve tumor shrinkage in locally advanced or metastatic HCC patients.

Age Eligible for study 18 years and older
Genders Eligible for Study Both
Key Inclusion Criteria
  1. Diagnosed hepatocellular carcinoma (HCC)
  2. No prior systemic therapy
  3. Have preserved liver function
Key Exclusion Criteria
  1. Patients with ascites uncontrolled by medication
  2. Patients with main portal vein tumor thrombosis or have extrahepatic disease
  3. Patients unable to swallow oral medications
 
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