Phase
Condition
Carcinoma
Treatment
atezolizumab plus bevacizumab
Clinical Study ID
Ages > 19 All Genders
Study Summary
Eligibility Criteria
Inclusion
The following two groups will be integrated and analyzed. The criteria for both groups are the same.
Group 1. Prospective Group
Inclusion Criteria
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
Exclusion Criteria
Patients who have systemic conditions accompanied by instability of vital signs, such as infections or organ failure
Those with mental/neurological conditions or dementia who have difficulties understanding and completing the consent form
Those who are assessed as not suitable for this study, at the discretion of the researcher
Group 2. Retrospective Group
Inclusion Criteria
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
Exclusion criteria
Patients who have systemic conditions accompanied by instability of vital signs, such as infections or organ failure
Those with mental/neurological conditions or dementia who have difficulties understanding and completing the consent form
Those who are assessed as not suitable for this study, at the discretion of the researcher
Study Design
Study Description
Connect with a study center
CHA Bundang Medical Center
Seongnam-si, Gyeonggi-do 13496
Korea, Republic ofActive - Recruiting

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