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Ongoing Clinical Trials

Phase II Trial of Avastin® in Pre- and Post- Transarterial Chemoembolisation for Unresectable Hepatocellular Carcinoma

Official Title A phase II single arm, multi-centre study of Bevacizumab (Avastin®) pre- and post- transarterial chemoembolisation (TACE) treatment for localised unresectable Hepatocellular Carcinoma (HCC)
Countries Hong Kong
Clinical Phase Phase II
Study Arm Single arm: All patients will receive Avastin combine with TACE
Description

Curative surgical or ablative therapies are indicated in 30-40% of HCC patients. However, for patients who are not suitable for curative therapies, other locoregional therapies such as transarterial chemoembolization (TACE), is indicated based on disease burden, liver function and performance status.

HCC is a hypervascular tumour. Tumour angiogenesis is essential for HCC growth, invasion, or metastasis. Tumour expression of vascular endothelial growth factor (VEGF), a potent stimulator of angiogenesis, is upregulated in HCC. Avastin is a humanized monoclonal antibody that binds VEGF to reduce its functional activity. It has been shown to be an effective anticancer drug in other cancers such as colorectal cancer.

The possible benefit of concurrent combination of bevacizumab and TACE as first-line therapy in patients with localized unresectable hepatocellular carcinoma will be investigated.

Age Eligible for study 18 years and older
Genders Eligible for Study Both
Key Inclusion Criteria
  1. Diagnosed hepatocellular carcinoma (HCC)
  2. Overall tumour lesions occupy < 50% of liver volume
  3. Have preserved liver function
Key Exclusion Criteria
  1. Have previously received any treatment for HCC
  2. Have previously received any biological agents
  3. Have extrahepatic disease
 
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