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Volumetric Analysis of Hepatocellular Carcinoma After Transarterial Chemoembolization

B

Brno University Hospital

Status

Completed

Conditions

Hepatocellular Carcinoma by BCLC Stage
Hepatocellular Carcinoma

Treatments

Procedure: Transarterial Chemoembolization

Study type

Observational

Funder types

Other

Identifiers

NCT04780789
01-080616/EK

Details and patient eligibility

About

The application of transarterial chemoembolisation (TACE) with drug-eluting beads in patients with hepatocellular carcinoma and its response to the treatment will be observed. The registry has the following objectives:

To assess the response to the treatment by standard methods and volumetric analysis as well as trying to determine any predictive response factors To determinate interobserver variability of the methods.

Full description

The patients with hepatocellular carcinoma in stage suitable for treatment by transarterial chemoembolization (TACE) with drug-eluting beads are included in the study. The investigators assess the response to the treatment by standard methods (RECIST, mRECIST) as well as by volumetric analysis. The size of tumor is evaluated on CT/MRI by two investigators prior to first TACE and then on all the check-ups (routinely every three months) until 31 December, 2019 or the patients' death.

Enrollment

61 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of HCC by a radiologist according to the European Association for the Study of the Liver (EASL) criteria or confirmed histologically
  • at least one TACE undergone at the University Hospital Brno
  • initial/ closing CT (Brillance 64, Philips, Netherlands; contrast enhancement 125 mL Iomeron 400, Bracco, Germany) or MRI study (Achieva, Philips, Netherlands, SENSE XL Torso coil 16 1.5T; contrast enhancement 15 mL Primovist, Bayer, Germany)
  • follow-up on or before December 31, 2019.

Exclusion criteria

  • when the inclusion criteria are not met.

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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