Actively Recruiting
Developing Atezolizumab-Bevacizumab Treatment Response Early Prediction Model in Advanced Hepatocellular Carcinoma Patients
Led by Seoul National University Hospital · Updated on 2025-05-15
170
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to develop a model to predict early treatment response in patients with advanced hepatocellular carcinoma, a type of liver cancer with a poor prognosis compared to other cancers. The study focuses on comparing the combination therapy of atezolizumab and bevacizumab with each drug alone, as there is currently no information on how to evaluate treatment response early for this combination. The goal is to improve understanding of treatment effects in this patient group. Participants in the study are adults aged 18 to 80 years diagnosed with advanced hepatocellular carcinoma who receive atezolizumab and bevacizumab every three weeks as first-line therapy. Before the second treatment cycle, blood tests and imaging are performed around week 5 to assess early response, followed by standard response evaluations between weeks 9 and 12. This observational study tracks patients receiving standard treatment without altering therapy. During the study, researchers monitor progression-free survival and overall survival, with follow-up continuing until June 22, 2025. Participants undergo blood and imaging tests to evaluate treatment response. The study excludes patients with severe contrast allergies or significant other health problems. Participation involves regular clinical visits and tests over the follow-up period, aiming to gather data for the predictive model.
CONDITIONS
Brief Title
Ate-Bev Early Response Prediction Model in Advanced HCC
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with advanced hepatocellular carcinoma
- Patients scheduled to receive atezolizumab-bevacizumab as first-line therapy
- Patients willing to participate in this study
- Adults aged between 18 and 80 years
You will not qualify if you...
- Individuals with a history of severe contrast allergy
- Individuals with severe comorbidities as defined by the American Society of Clinical Oncology-Friends of Cancer Research Organ Dysfunction
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 weeks
Participants receive atezolizumab and bevacizumab every three weeks with blood tests and imaging tests conducted before the second treatment cycle to evaluate early response.
Approximately 2 visits (in-person)
Duration - Up to 2 years
Participants are followed to assess progression-free survival and overall survival until June 22nd, 2025.
Follow-up visits as scheduled by healthcare providers
Trial Site Locations
Total: 1 location
1
Seoul National University Hospital
Seoul, South Korea
Actively Recruiting
Research Team
J
Jeong-Hoon Lee, MD PhD
H
Hyunjae Shin, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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