Contribution of F-18 Fluoro-Deoxy-Glucose PET/CT (Positron Emission Tomography) to the Assessment of HCC (Hepato-cellular Carcinoma) Treatment Efficiency
NCT ID: NCT01322477
Last Updated: 2011-03-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
25 participants
OBSERVATIONAL
Brief Summary
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Recurrence rate is very high, and extrahepatic disease develops in about 30% of the cases and in up to 20% after liver transplantation.
Systemic treatment is thus an option. Sorafenib (multi-kinase inhibitor) is the first agent to significantly improve the overall survival in advanced HCC. However, the drug has serious side effects and is very expensive.
PET/CT with F18-FDG is a common tool for systemic evaluation and staging of various tumors.
The value of the FDG PET for evaluation of HCC is controversial, in particular due to the unique metabolic pathway of glucose in the HCC cells. Since 2007 more and more studies suggest the feasibility of FDG PET/CT for monitoring local recurrence (especially after RF) and metastatic spread of HCC, including detection of active disease only suspected by AFP (alphafoetoprotein) elevation.
Early detection of treatment response to therapy by whole body FDG PET/CT allows for change of treatment as early as possible,when the tumor is non-responsive before serious side effects appear or before depletion of body resources.
The aim of our study is to investigate the contribution of FDG PET/CT to assessment of treatment response.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Hepatocellular Carcinoma
Patients with advanced HCC
F18-FDG PET/CT
Interventions
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F18-FDG PET/CT
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Other liver disease (e.g. metastases and benign lesions)
18 Years
80 Years
ALL
No
Sponsors
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Hadassah Medical Organization
OTHER
Locations
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Hadassah Hebrew University Medical Center
Jerusalem, , Israel
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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0022-11-HMO
Identifier Type: -
Identifier Source: org_study_id
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