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Use of the PET/CT [18F]-Fluorocholine: Diagnostics and Follow-up of Hepatocellular Carcinoma

Use of the PET/CT [18F]-Fluorocholine: Diagnostics and Follow-up of Hepatocellular Carcinoma - FCH PET/CT and HCC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36749
Enrollment
100
Registered
2011-03-03
Start date
2010-11-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hepatocellular carcinoma livercancer

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. 18 years of age or older 2. Signed informed consent 3. Affirmed or suspected diagnosis of HCC based on current standard of care and guidelines 4. Expected (partial) treatment and follow-up at the AMC

Exclusion criteria

Exclusion criteria: Exclusioncriteria in regard to the multiphase CT scan combined with the PETscan include: 1.1. Renal impairment and allergy to the contrast agent. These patients undergo pre-treatment according to the AMC radiology protocol, after which the combined FCH PET / (multiphase) CT scan will be performed. 1.2. If patients cannot undergo the multiphase CT scan, an MRI is performed instead and FCH PET/CT is made with a low dose CT scan and no contrast is used. 1.3. If however no imaging studies with CT or MR are possible, because of contraindications against both imaging modalities, patient is excluded.

Design outcomes

Primary

MeasureTime frame
For further details see - Protocol section: 2 - 1. Sensitivity and specificity of the FCH PET/CT scan ( in reference to current golden standard of: ) - Histological outcome (and differentiation of the tumor) OR: - Outcome of imaging results corresponding with HCC

Secondary

MeasureTime frame
For further details see - Protocol section: 2 - 1. Diagnosis of HCC, spread of the disease or metastatic disease in an earlier stage, compared to diagnosis with conventional imaging modalities. 2. Change in treatment 3. Differentiation grade of the HCC based on the SUV-ratio (golden standard is histological outcome)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)