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Comparison of Response and Recurrence Rates Following Percutaneous Microwave Coagulation Therapy Versus Percutaneous Radiofrequency Ablation (Thermoablation)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Completed

Conditions

Chronic Liver Disease
Hepatocellular Carcinoma
Thermoablation

Treatments

Other: Percutaneous Radiofrequency Ablation
Other: Percutaneous Microwave Ablation

Study type

Interventional

Funder types

Other

Identifiers

NCT02859753
GUIU MicroS 2012

Details and patient eligibility

About

To date, the majority of studies that have evaluated the efficacy of microwave ablation (MWA) in the treatment of hepatocellular carcinoma (HCC) lesions in cirrhotic patients and compared its efficacy with that of percutaneous radiofrequency ablation (RFA) for local recurrence and survival have been retrospective. There have been no prospective randomized studies comparing percutaneous microwave ablation (PMWA) with RFA for ablated tumour volume, the response after one session, local recurrence rates in the first year, complication rates and survival at 3 and 5 years for HCC lesions > 2 cm in patients with Child-Pugh A and B cirrhosis. The hypothesis the investigators wish to explore is that though the 2 methods are equivalent for lesions ≤ 2 cm, MWA could show better efficacy with a similar risk for lesions > 2 cm and for lesions close to vessels ≥ 3 mm in diameter, as shown in retrospective studies.

Enrollment

35 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient who have been informed about the research and given their oral consent
  • Patients with national health insurance cover
  • Patients ≥ 18 years
  • ≤ 3 CHC lesions ≤ 4 cm, with a maximum of 3 lesions with a diagnosis of HCC based on histology, or according to European Society for the Study of the Liver (EASL) criteria
  • Chronic liver disease or cirrhosis with a Child-Pugh score between 5 and 8 points
  • Contra-indication for surgical resection at the time of the therapeutic decision made during a multidisciplinary meeting

Exclusion criteria

  • Informed consent not obtained (refusal of patient or patient lacking discernment)
  • Kidney failure with creatinine clearance < 30 ml/min thus preventing the injection of contrast for the initial or follow-up radiological imaging
  • Presence of a malignant tumour other than the HCC at the time of the diagnosis, unless a basocellular carcinoma
  • Cirrhosis with a Child-Pugh score > 8
  • Contra-indication for percutaneous treatment according to Barcelona Clinic Liver Cancer (BCLC) criteria
  • Patients without national health insurance cover

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

35 participants in 2 patient groups

RFA
Experimental group
Treatment:
Other: Percutaneous Radiofrequency Ablation
MCT
Active Comparator group
Treatment:
Other: Percutaneous Microwave Ablation

Trial contacts and locations

1

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Central trial contact

Boris GUIU

Data sourced from clinicaltrials.gov

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