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Contribution of F-18 Fluoro-Deoxy-Glucose PET/CT (Positron Emission Tomography) to the Assessment of HCC (Hepato-cellular Carcinoma) Treatment Efficiency

H

Hadassah Medical Center

Status

Unknown

Conditions

Hepatocellular Carcinoma

Treatments

Other: F18-FDG PET/CT

Study type

Observational

Funder types

Other

Identifiers

NCT01322477
0022-11-HMO

Details and patient eligibility

About

HCC (Hepato-cellular Carcinoma) is the fifth most frequent cancer in humans and its prevalence is growing. The most effective treatment of HCC is surgical and includes resection and liver transplantation; however, only 20% of the patients can be treated surgically. Local interventional therapy, such as radiofrequency (RF) ablation and transarterial embolization is also used.

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.

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • advanced HCC for systemic treatment

Exclusion criteria

  • HCC only localized in liver,
  • Other liver disease (e.g. metastases and benign lesions)

Trial design

25 participants in 1 patient group

Hepatocellular Carcinoma
Description:
Patients with advanced HCC
Treatment:
Other: F18-FDG PET/CT

Trial contacts and locations

1

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Central trial contact

Roland Chisin, MD; Marina Orevi, MD

Data sourced from clinicaltrials.gov

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