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Small and Steatotic Hepatocellular Carcinoma

Small and Steatotic Hepatocellular Carcinoma : a Distinctive Radiological Variant With Improved Outcome After Percutenous Ablation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03428321
Enrollment
238
Registered
2018-02-09
Start date
2015-01-01
Completion date
2019-12-30
Last updated
2020-05-06

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

Conditions

HCC

Keywords

Microwave ablation, Percutaneous thermalablation, High risk location, Articifial pneumothorax, Lipiodol marked, Prognostic factor

Brief summary

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.

Detailed 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

Interventions

None listed

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Thermal ablations1 dayEvaluation of thermal ablations (radiofrequency and microwave ablation)

Countries

France

Outcome results

None listed

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