TAE and MWA Combination Therapy in Early-stage Hepatocellular Carcinoma
Hepatocellular Carcinoma, Hepatoma, Liver Cancer, Adult

About this trial
This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Therapeutic Embolization, Ablation Techniques, Transarterial Embolization, TAE, Microwave Ablation, MWA
Eligibility Criteria
Inclusion Criteria:
- Primary diagnosis of hepatocellular carcinoma (HCC)
- HCC classification of stage 0 (very early) or stage A (early) according to Barcelona Clinic Liver Cancer (BCLC) staging system criteria
- Adequate clinical condition to undergo laparoscopic or robot-assisted laparoscopic transarterial embolization (TAE) and/or microwave ablation (MWA) as treatment for HCC
- Willing and able to give informed consent
Exclusion Criteria:
- Radiologic (computed tomography or magnetic resonance imaging) evidence of invasion into major portal/hepatic venous branches and no extrahepatic metastases
- Evidence of residual disease at first post-MWA computed tomography examination
- Body Mass Index (BMI) > 35
- Previous history of hepatic resections
- Severe renal dysfunction (creatinine clearance of <40 mL/min)
- Pregnant or nursing women
Sites / Locations
- Carolinas Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
TAE + MWA combination therapy
MWA monotherapy
In patients randomized to receive the experimental therapy, transarterial embolization (TAE) treatments will be initiated within one week of randomization. Blunt embolization will be performed with LC beads with a maximum size of 700 µm. Microwave ablation (MWA) will be performed up to one month following randomization. The LC beads will be admixed with 8-15 mL of contrast and injected into the arterial branch at a rate of 1-2 mL/min. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request.
Microwave ablation (MWA) will be performed up to one month following randomization. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request. All operative MWAs will be performed in a laparoscopic or robot-assisted laparoscopic setting. All ablations will be guided by intraoperative ultrasound. Ablations will be performed with a 2.45-GHz generator with a 1.8-mm-diameter transcutaneous antenna.