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A retrospective study of the efficacy and safety of HAIC combined with Renvastinib and tirellizumab versus TACE combined with Renvastinib and tirellizumab in the treatment of advanced hepatocellular carcinoma

A retrospective study of the efficacy and safety of HAIC combined with Renvastinib and tirellizumab versus TACE combined with Renvastinib and tirellizumab in the treatment of advanced hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096470
Enrollment
Unknown
Registered
2025-01-24
Start date
2025-02-05
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

advanced hepatocellular carcinoma

Interventions

Exposed group:HAIC was administered in combination with lenvatinib and tirellizumab
Non-exposed group:TACE was administered in combination with lenvatinib and tirellizumab

Sponsors

Affiliated Hospital of Guangdong Medicine University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patient age > 18 years old, no gender requirement; 2.Pathological or clinical diagnosis of unresectable hepatocellular carcinoma; 3. American Eastern Oncology Consortium (EC0C) or Activity Status (PS) score 0-1; 4.Child-Pugh grade A/B ;5.No previous systematic treatment ;6.Complete clinical data:

Exclusion criteria

Exclusion criteria: 1.Patients who are allergic to the drug being studied; 2. combined with other serious diseases such as serious heart disease and cerebrovascular embolism; 3. Exclude patients with active infectious diseases, such as active tuberculosis, syphilis, etc.; 4. pregnant or lactating women, who are in the fertile period and do not take effective contraceptive measures;

Design outcomes

Primary

MeasureTime frame
Overal Survival;Progression-Free Survival;

Secondary

MeasureTime frame
Objective remission rate;Disease control rate;Safety (including adverse event rate (AES), Serious Adverse Event (SAE));

Countries

China

Contacts

Public ContactLiang Qilian

Affiliated Hospital of Guangdong Medicine University

13822522910@163.com+86 138 2252 2910

Outcome results

None listed

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