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Role PET Imaging in Response Assessment for Hepatocellular Carcinoma (HCC)

Phase 1
Completed
Conditions
Primary Liver Cancer
Interventions
Procedure: MRI of the liver before start of treatment
Procedure: MRI after treatment
Procedure: PET-scan before treatment start
Procedure: PET scan after treatment
Registration Number
NCT01116804
Lead Sponsor
University Hospital, Ghent
Brief Summary

Present imaging modalities for primary liver cancer (hepatocellular carcinoma or HCC) have several shortcomings. One important shortcoming is the time delay between successful treatment and radiological confirmation of this response. Often it takes several months for anatomical changes to occur and to be appreciated on morphological imaging such as CT or MRI (shrinkage of tumor, absence of contrast enhancement). Functional imaging by means of Fluor-18 deoxyglucose or Fluor-18 Choline (positron emitters, PET-scan) might be an early indicator of response. This "early" information might help to tailor treatment. For instance, if no response is induced, an early switch in therapy can be planned.

The present study investigates whether the routine PET-tracer (Fluor-18 deoxyglucose) and the experimental PET-tracer, Fluor-18 Choline help to predict response if a patient with inoperable primary liver cancer is treated (radionuclide therapy, biologicals).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
inoperable liver cancer patientsMRI after treatment-
inoperable liver cancer patientsMRI of the liver before start of treatment-
inoperable liver cancer patientsPET-scan before treatment start-
inoperable liver cancer patientsPET scan after treatment-
Primary Outcome Measures
NameTimeMethod
To evaluate the efficacy of PET-imaging versus classic response assessment (MRI, CT-scam) in patients with inoperable liver cancer6 months after start of treatment
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital Ghent

🇧🇪

Ghent, Belgium

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