About this trial
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
Eligibility criteria
Qualifiers
A single liver tumor, ≤ 2 cm, classified as BCLC stage 0 (very early stage).
Tumors ≤ 3 in number, each ≤ 3 cm, or a single tumor ≤ 5 cm, classified as BCLC stage A (early stage) liver cancer.
ECOG performance status of 0.
Age ≥ 18 years.
Disqualifiers
A single tumor > 5 cm, or multiple tumors > 3 cm.
Diffuse hepatocellular carcinoma.
Vascular invasion (e.g., portal vein obstruction).
Extrahepatic tumor spread.
Trial design
Treatments tested in this trial
- Ga-68 Dolacga PET scan