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Ga-68 Dolacga PET Scan in HCC Under RFA

The Role of Ga-68 Dolacga PET Scan in Patients With Hepatocellular Carcinoma Under Radiofrequency Ablation

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06792097
Acronym
HCC; RFA
Enrollment
10
Registered
2025-01-24
Start date
2025-02-01
Completion date
2026-12-31
Last updated
2025-01-24

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

Conditions

Computed Tomography, Deep Learning, Hepatocellular Carcinoma (HCC), PET Scan, Radiofrequency Ablation

Keywords

Hepatocellular carcinoma, Radiofrequency ablation, Ga-68 Dolacga PET scan, Liver function, Neural network, Radiomics

Brief summary

This study aims to investigate the use of Ga-68 Dolacga PET scan technology to assess treatment response and liver function changes in patients of early-stage liver cancer receiving RFA. The main questions it aims to answer are: 1. How to assess treatment response and liver function changes in hepatocellular carcinoma patients undergo RFA via Ga-68 Dolacga PET scan? 2. Compared with computed tomography (CT) scans, how effective is Ga-68 Dolacga PET scan for treatment response assessment? 3. What is the correlation between Ga-68 Dolacga PET scan findings and patient treatment outcomes by tracking liver function and tumor recurrence after RFA? Participants will: 1. Undergo Ga-68 Dolacga PET scans and computed tomography before and one month after RFA treatment, followed by monitoring every three months thereafter. 2. Total liver functional volume and residual liver functional volume are obtained from Ga-68 Dolacga PET scan

Detailed description

This study aims to investigate the use of Ga-68 Dolacga PET scan technology to assess treatment response and liver function changes in patients of early-stage liver cancer receiving RFA. This study also compares the results of Ga-68 Dolacga PET scans with computed tomography (CT) scans and evaluate the correlation between Ga-68 Dolacga PET scan findings and patient treatment outcomes by tracking liver function and tumor recurrence after RFA. This study adopts a prospective clinical trial design, enrolling patients with early-stage liver cancer and undergoing RFA treatment. Clinical data, laboratory results, serum, biopsy tissues for pathology and relevant imaging findings are collected for analysis. Participants undergo Ga-68 Dolacga PET scans and CT before and one month after RFA treatment, followed by monitoring every three months thereafter. Quantitative analysis utilizes region of interest techniques to measure standardized uptake values (SUV). Total liver functional volume and residual liver functional volume are obtained from Ga-68 Dolacga PET scan injection dose percentages and SUV values. Changes in liver storage capacity as determined by Ga-68 Dolacga PET scans are evaluated and correlated with traditional laboratory liver function tests and imaging evaluations.

Interventions

DIAGNOSTIC_TESTGa-68 Dolacga PET scan

Contrast Name: Nuclear Medicine Dolacga (Lyophilized product for the preparation of gallium Ga68 Dolacga injection). Active Ingredient, Dosage, Route: NOTA-Hexa lactoside (INER038), 40 micrograms, IV injection. PET Imaging Schedule: Before radiofrequency ablation therapy, one month after ablation therapy, and follow-up every three months thereafter.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with hepatocellular carcinoma (BCLC stage 0 and stage A) eligible for radiofrequency ablation (RFA) treatment exhibit the following characteristics: 1. A single liver tumor, ≤ 2 cm, classified as BCLC stage 0 (very early stage). 2. Tumors ≤ 3 in number, each ≤ 3 cm, or a single tumor ≤ 5 cm, classified as BCLC stage A (early stage) liver cancer. 3. ECOG performance status of 0. 4. Age ≥ 18 years.

Exclusion criteria

* Intermediate (BCLC B stage) and advanced (BCLC C stage) liver cancer patients: 1. A single tumor \> 5 cm, or multiple tumors \> 3 cm. 2. Diffuse hepatocellular carcinoma. 3. Vascular invasion (e.g., portal vein obstruction). 4. Extrahepatic tumor spread. * Early-stage liver cancer (BCLC A stage): 1. Contraindications for radiofrequency ablation (RFA). 2. Target lesions previously treated with local therapies, including surgical resection, percutaneous ethanol injection (PEI), or liver transplantation.

Design outcomes

Primary

MeasureTime frameDescription
Patient liver reserve capacity before and after radiofrequency ablation therapy2 yearsExpressed as percentage of injected dose (%ID) and standardized uptake value (SUV). 1. Correlation with patients' baseline characteristics, laboratory data, tumor characteristics 2. Compared with ICG test 3. Compared with computed tomography 4. Correlation with patients' overall survival, progression free survival, objective response rate

Contacts

Primary ContactJa-Der Liang, MD, phD
jdliangntu@ntu.edu.tw+886 0223123456
Backup ContactGeng-Hao Bai, MD
b101105010@gmail.com+886953861233

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026