Investigation of Predictive Biomarkers in Patients With Advanced Hepatocellular Carcinoma Treated With Atezolizumab Plus Bevacizumab

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about in patients with advanced hepatocellular carcinoma treated with atezoliozumab and bevacizumab. In this clinical study, we intend to analyze the multiomics data by analyzing the peripheral blood and tumor tissue before and after treatment of patients with advanced liver cancer receiving systemic drug treatment, and analyzing the correlation with the treatment. This is an exploratory study that aims to discover biomarkers that are highly correlated with treatment response.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Those above the age of 20 who understand the purpose of the study and agree to participate in the collection of samples during the study.

• Patients who have been diagnosed with unresectable advanced HCC through imaging, histological, or cytological tests.

• Patients who underwent an NGS test with advanced HCC tissues

• Patients planning to receive atezolizumab and bevacizumab combination therapy

• Patients with measurable lesions based on RECIST v1.1

• ECOG performance status 0 or 1

• Patients with a life expectancy of at least three months

• Those above the age of 20 who understand the purpose of the study and agree to participate in the collection of samples during the study.

• Patients who have been diagnosed with unresectable advanced HCC through imaging, histological, or cytological tests.

• Patients who underwent an NGS test with advanced HCC tissues

• Patients have received atezolizumab and bevacizumab combination therapy

• Patients with measurable lesions based on RECIST v1.1

• ECOG performance status 0 or 1

• Patients with a life expectancy of at least three months

Locations
Other Locations
Republic of Korea
CHA Bundang Medical Center
RECRUITING
Seongnam-si
Contact Information
Primary
Hong Jae Chon, MD,PhD
minidoctor@cha.ac.kr
82-031-780-3928
Time Frame
Start Date: 2021-08-02
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 100
Treatments
analytic group
advanced HCC Patients
Related Therapeutic Areas
Sponsors
Leads: CHA University
Collaborators: Boryung Pharmaceutical Co., Ltd

This content was sourced from clinicaltrials.gov