A Randomized, Multicenter, Open-Label, Phase II Trial of Atezolizumab Plus Bevacizumab Alone or Combined with External Beam RadioTherapy for HepatoCellular Carcinoma with Macrovascular Invasion (ALERT-HCC)

Status: Recruiting
Location: See location...
Intervention Type: Drug, Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The recent global IMbrave150 study evaluated the combination of atezolizumab and bevacizumab versus sorafenib in 501 patients with advanced or metastatic Hepatocellular Carcinoma (HCC). The median overall survival (OS) was notably better in the atezolizumab/bevacizumab group. However, for HCC patients with intrahepatic macrovascular invasion (MVI), the prognosis remains poor, indicating a significant unmet need in this group. External Beam Radiotherapy (EBRT) has shown promising results in treating HCC with MVI, especially when used in combination with trans-arterial chemoembolization (TACE). It has been reported that radiotherapy may make tumor cells more susceptible to immune-mediated therapy, potentially enhancing the effects of atezolizumab and bevacizumab. Thus, this study aims to investigate the efficacy and safety of atezolizumab/bevacizumab alone versus atezolizumab/bevacizumab in combination with EBRT in HCC patients with macrovascular invasion.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 79
Healthy Volunteers: f
View:

• Older than 19 years of age, lower than 80 years of age

• Child-Pugh class A hepatic function

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1

• Patients with HCC \[diagnosed according to AASLD guidelines\] invading the intrahepatic vascular system

• No prior systemic therapy for HCC

• At least one measurable HCC lesion with ≥ 1cm diameter

• Adequate hematologic and organ function

‣ Hemoglobin ≥ 9.0 g/dL

⁃ Absolute neutrophil count ≥ 1,000 /mm3

⁃ Platelet ≥ 50,000/ mm3 without transfusion

• Total bilirubin ≤ 2.5 mg/dL

Locations
Other Locations
Republic of Korea
Asan Medical Center
RECRUITING
Seoul
Contact Information
Primary
Jihyun An
starlit1@naver.com
82-31-560-2209
Backup
Ju Hyun Shim
s5854@amc.seoul.kr
Time Frame
Start Date: 2022-10-22
Estimated Completion Date: 2026-03
Participants
Target number of participants: 138
Treatments
Experimental: Radiotherapy combination
Atezolizumab+Bevacizumab, combined EBRT to vascular invasion~* Atezolizumab will be administered by IV, 1200 mg on day 1 of each 21day cycle.~* Bevacizumab will be administered by IV, 15 mg/kg on day 1 of each 21day cycle.~* The external beam radiotherapy will commence after day 2 of the first cycle of A+B, and will be delivered in accordance with institutional protocol.
Active_comparator: Atezolizumab+Bevacizumab
* Atezolizumab will be administered by IV, 1200 mg on day 1 of each 21day cycle.~* Bevacizumab will be administered by IV, 15 mg/kg on day 1 of each 21day cycle.
Related Therapeutic Areas
Sponsors
Collaborators: Seoul National University Hospital, Soon Chun Hyang University, Hanyang University
Leads: Asan Medical Center

This content was sourced from clinicaltrials.gov