RecruitingNCT07378709

Exploratory Blood-Based Biomarkers in TACE-Treated Hepatocellular Carcinoma

Blood-Based Biomarkers for Prediction and Monitoring of Response to TACE in Hepatocellular Carcinoma: A Pilot Study


Sponsor

University of Belgrade

Enrollment

15 participants

Start Date

Aug 21, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this observational study is to evaluate changes in selected biomarkers and their potential connection with early radiological outcomes in adult patients with hepatocellular carcinoma (HCC) who are candidates for Transarterial Chemoembolization (TACE) treatment. The main questions it aims to answer are whether specific biomarkers change in response to TACE treatment and if there is a correlation between these changes and early radiological treatment response as measured by Modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria. Participants will undergo standard-of-care TACE as decided by a multidisciplinary team and will provide blood samples at predefined, clinically relevant time points, specifically before the first TACE procedure and during subsequent follow-up cycles on the day of either a new TACE or a control Computed Tomography (CT) scan. Additionally, participants will undergo routine clinical and radiological assessments, including multiphase CT or Magnetic Resonance Imaging (MRI) scans four to eight weeks after the procedure to monitor treatment success, with all data being collected from medical records and standard diagnostic procedures.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study explores whether blood-based biomarkers (measurable substances in the blood) can predict how well liver cancer patients respond to a procedure called TACE (transarterial chemoembolization), which delivers chemotherapy directly to liver tumors while blocking their blood supply. **You may be eligible if...** - You are 18 or older with a confirmed diagnosis of hepatocellular carcinoma (liver cancer) - You are scheduled to receive TACE as part of your standard treatment - Your liver function score (Child-Pugh) is 7 or below - You are in good overall health (ECOG performance status of 0) - You are able to return for follow-up scans 4–8 weeks after TACE **You may NOT be eligible if...** - Your liver function score is 8 or higher - Your cancer has spread outside the liver or has invaded major blood vessels - TACE is not technically feasible for your tumor - You have severe blood clotting problems or are pregnant or breastfeeding - You are allergic to iodine contrast dye Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

KBC Bežanijska kosa

Belgrade, Serbia

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07378709


Related Trials