About this trial
To determine the efficacy and safety of atezolizumab-bevacizumab combination therapy plus stereotactic body radiotherapy(SBRT) in patients with advanced hepatocellular carcinoma, Subjects will start SBRT for one or more primary cancers and/or metastatic lesions and no more than 5 sites within two month before and after the start date of atezolizumab-bevacizumab combination therapy.
In this study, it is expected to improve the treatment response rate of atezolizumab-bevacizumab therapy, which is currently first-line chemotherapy but has a low treatment response rate.
Eligibility criteria
Qualifiers
Age 19 to 80 years old
Liver function Child-Pugh class A
ECOG 0-1
Patient clinically or pathologically diagnosed with hepatocellular carcinoma
Disqualifiers
Brain metastases
Have a history of malignancy other than hepatocellular carcinoma within the last 5 years (except for malignancies with little risk of metastasis or death, e.g., adequately treated cervical carcinoma in situ, non-melanoma skin cancer, localized prostate cancer, tubular carcinoma in situ, or stage 1 uterine cancer.)
Subjects with a high probability of untreated gastric or esophageal varices or bleeding
Serious uncontrolled medical comorbidities
Trial design
Treatments tested in this trial
- Stereotactic body radiotherapy