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Effectiveness and Safety of Atzeolizumab and Bevacizumab among patients with unresectable hepatocellular carcinoma in real-world clinical practice in China

Effectiveness and Safety of Atzeolizumab and Bevacizumab among patients with unresectable hepatocellular carcinoma in real-world clinical practice in China

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109767
Enrollment
Unknown
Registered
2025-09-24
Start date
2024-06-28
Completion date
Unknown
Last updated
2025-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unresectable hepatocellular carcinoma

Interventions

observation group:None

Sponsors

Xi'an International Medical Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged >= 18 years at the initiation of Atezo/Bev; 2.Initiating Atezo/Bev between 28 October 2020 and 31 December 2023; 3.Diagnosed with unresectable HCC as evidenced clinically or by radiology, histology or cytology before or at the initiation of Atezo/Bev. The evidence of being diagnosed as "unresectable" may include but is not limited to below: o "Unresectable" or "advanced" directly documented in the medical records o History of extrahepatic metastasis as evidenced clinically or by radiology, histology or cytology OR China Liver Cancer (CNLC) Stage IIIb; 4.At least one visit record after the initiation of Atezo/Bev;

Exclusion criteria

Exclusion criteria: 1.Diagnosed with concomitant cancer except for basal cell carcinoma before or at the initiation of Atezo/Bev; 2.Participating in interventional clinical studies before or at initiating Atezo/Bev;

Design outcomes

Primary

MeasureTime frame
Real-world overall survival;TRAE, SAE, and AE related death;

Secondary

MeasureTime frame
Demographics and vital signs;Clinical characteristics;Time to discontinuation;Time to next treatment;Serum alpha-fetoprotein (AFP) reduction;Prothrombin induced by the absence of vitamin K or antagonist-II (PIVKA-II) reduction;Liver function abnormality;Renal function abnormality;Hemorrhage;rwPFS;Hepatitis virus reactivation;Immune-related adverse events;

Countries

China

Contacts

Public ContactHan Guohong

Xi'an International Medical Center Hospital

13991969930@126.com+86 29 6830 2656

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026