Evaluation of molecular biomarkers for hepatocellular carcinoma (HCC) therapy
- Conditions
- Liver CancerHepatocellular CarcinomaLiver CirrhosisOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colonCancer - Liver
- Registration Number
- ACTRN12623000762651
- Lead Sponsor
- A/Prof Adam Testro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Study question 1:
1.Age 18 or greater
2.Adult patients undergoing therapy for Hepatocellular Carcinoma (HCC)
a.Therapy may include 3 broad categories
i.Interventional radiology
1.Transarterial Chemo-embolisaion (TACE)
2.Microwave ablation (MWA)
3.Radiofrequency ablation (RFA)
4.Selective Internal Radiation-Therapy (SIRT)
5.Percutaneous Ethanol Injection (PEI)
ii.Surgery
1.Liver resection
2.Liver transplantation
iii.Radiation oncology
1.Stereotactic Body Radiation Therapy (SBRT)
iv.Medical oncology
1.Systemic therapy
v.Other
3.Informed consent
Study Question 2:
1.Age 18 or greater
2.Adult patients diagnosed with HCC
a.Referred to the HCC Multi-disciplinary meeting for consideration of liver transplant assessment or
b.Referred to the pre-liver transplant clinic for consideration of liver transplant assessment
3.Patients must have been informed by a clinician from the Liver Transplant Unit that they are being considered for liver transplant assessment, with documentation in medical records
a.Patients may or may not yet have been formally assessed or wait listed for liver transplantation
4.Patients may or may not have undergone prior therapy for HCC
5.Informed consent
1.Unable to consent
2.Withdrawal of consent
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method