Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID05763277

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

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Monitoring

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

Loading map...

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

Similar Trials

Clinical Impact of 18F-FDGal PET/CT and PET/MRI in Patients ...

Hepatocellular Carcinoma

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here