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A retrospective study on the treatment of hepatocellular carcinoma with different doses of bevacizumab combined with sintilimab and TACE/HAIC

A retrospective study on the treatment of hepatocellular carcinoma with different doses of bevacizumab combined with sintilimab and TACE/HAIC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129193
Enrollment
Unknown
Registered
2026-07-31
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Hepatocellular carcinoma

Interventions

Reduced-dose bevacizumab in combination with TACE and/or HAIC plus sintimab for the treatment of HCC patients:None
Standard-dose bevacizumab in combination with TACE and/or HAIC plus sintimab for the treatment of HCC patients:None

Sponsors

HenanCancerHospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. Confirmed diagnosis of hepatocellular carcinoma (HCC) based on imaging or pathological criteria; 3. Unresectable disease and having received at least one cycle of transcatheter arterial chemoembolization (TACE) and/or hepatic arterial infusion chemotherapy (HAIC) in combination with at least two cycles of sintilimab and a bevacizumab biosimilar; 4. At least one measurable lesion per RECIST version 1.1 criteria; 5. Eastern Cooperative Oncology Group (ECOG) performance status of 0–2; 6. Child-Pugh class A or B (score <= 7); 7. Barcelona Clinic Liver Cancer (BCLC) stage B or C; 8. Availability of complete baseline and follow-up data.

Exclusion criteria

Exclusion criteria: 1. Prior systemic or locoregional therapy for hepatocellular carcinoma; 2. Concurrent malignancy or history of other malignancies within the past 5 years; 3. Incomplete clinical data or loss to follow-up; 4. Subsequent receipt of surgical resection; 5. Non-standard or non-protocol-compliant treatment.

Design outcomes

Primary

MeasureTime frame
Objective remission rate;

Secondary

MeasureTime frame
Disease control rate;Overall survival;

Countries

China

Contacts

Public ContactHang Yuan

HenanCancerHospital

934266242@qq.com+86 371 65587372

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026