Clinical Trial

Validation of Blood-Based Biomarkers in TACE-Treated Hepatocellular Carcinoma

Study acronym: BLOOD-TACE-M
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
The goal of this prospective observational study is to validate the clinical utility of specific blood-based biomarkers for predicting and monitoring treatment response in patients with hepatocellular carcinoma (HCC) undergoing Transarterial Chemoembolization (TACE). The study aims to determine if longitudinal changes in these biomarkers can reliably correlate with early radiological treatment response, as measured by Modified Response Evaluation Criteria in Solid Tumors (mRECIST). Participants will receive standard-of-care TACE treatment and will provide blood samples at baseline and during subsequent clinical follow-up cycles. Biomarker levels will be compared against routine multiphase computed tomography (CT) or Magnetic Resonance Imaging (MRI) scans performed four to eight weeks post-procedure to establish their accuracy as predictive tools for clinical success.
Trial Details
NCT Number NCT07414433
Lead Sponsor University of Belgrade
Conditions Hepatocellular Carcinoma (HCC), Liver Neoplasms
Enrollment 60 participants
Start Date 2026-03-01
Primary Completion 2029-03-30 (estimated)
Study Completion 2029-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-02-17