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Small and Steatotic Hepatocellular Carcinoma

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

HCC

Study type

Observational

Funder types

Other

Identifiers

NCT03428321
RECHMPL17_0436

Details and patient eligibility

About

Percutaneous thermoablation in an effective local curative treatment in patients with cirrhosis and HCC smaller than 3 cm in diameter (BCLC 0-A).

Around 30% of HCC patients referred for percutaneous ablation were regarded as non-feasible because of a difficult-at risk location or undetectable nodules.

We used percutaneous thermoablation to treat HCC on high risk locations (subcapsular or liver dome) with or without lipiodol marked (for undetectable HCC).

No clinical study has been published so far to compare percutaneous thermoablation of HCC on liver dome CT guided with artificial pneumothorax and lipiodol marked, and percutaneous thermoablation of HCC guided by ultrasonography (non subcapsular, distent form diaphragm).

This retrospective study evaluate the overall survival, the local tumor progression or distant liver progression after percutaneous ablation for HCC and determine prognostic factors.

Full description

We performed 412 percutaneous thermoablations on 238 patients for HCC between January 2015 and November 2019.

All thermoablation procedures were performed percutaneously under ultrasound or CT guidance, with ou without artificial pneumothorax or ascites, with ou without lipiodol marked.

Purposes:

  • Tumor response upon mRECIST criteria
  • Progression-free survival
  • Overall survival
  • Local tumor progression
  • Distent liver progression
  • Prognostic factors

Enrollment

238 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HCC according to histological examination or Barcelona criteria
  • BCLC0 or A
  • Measurable targets according to mRECIST v1.1
  • Child A or B7 cirrhosis
  • HCC < 4 cm, < 3 nodules, Age ≥ 18 years
  • No extrahepatic metastasis, no vascular invasion
  • Performance status 0 or 1
  • Thrombocytes ≥ 50 000/mm3, TP > 50%

Exclusion criteria

  • Follow-up < 1month
  • Lobar/main portal venous thrombus
  • Abundant ascites
  • Antecedent of bilio-digestive anastomosis or endoscopic sphincterotomy
  • Combined treatment with embolization or chemo-embolization

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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