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Prospective study of TACE-HAIC combined with lenvatinib and Tislelizumab in the treatment of unresectable HCC

Prospective study of TACE-HAIC combined with lenvatinib and Tislelizumab in the treatment of unresectable HCC

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067362
Enrollment
Unknown
Registered
2023-01-05
Start date
2023-02-22
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

hepatocellular carcinoma

Interventions

experimental group:TACE-HAIC combined with lenvatinib and tirelizumab for unresectable HCC

Sponsors

The Second People's Hospital of Yibin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. HCC patients with BCLC B or C stage and unresectable after surgical evaluation; 2. Age 18-75 years old; 3. At least one measurable intrahepatic lesion; 4. Have not received local and systemic treatment for liver cancer in the past; 5. Liver function Child-Pugh grade A or B (CP-7B) and ECOG score = 3.0 × 10^9/L or absolute neutrophil count > 1.5 × 10^9/L, hemoglobin >= 8 g/dL, platelet count > 60 × 10^9/L; 7. Renal function: serum creatinine level 45%; 10. Patients who are not allergic to contrast media; patients who are informed and agree to participate in this study, have good clinical compliance, and are expected to survive for more than 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with other malignant tumors in the past; 2. Combined with organic diseases of important organs such as heart and kidney; 3. Previously received systemic treatment for liver cancer; 4. Hepatic decompensation (Child-Pugh C grade of liver function); 5. Patients with severe infectious diseases (> grade 2 infection; requiring antibiotic or surgical intervention or life-threatening infection); 6. Patients with diffuse liver cancer lesions and history of upper gastrointestinal bleeding or ascites; 7. Pregnancy or breastfeeding; 8. Severe allergy to contrast medium or other drugs; 9. Incomplete clinical data; lost to follow-up, patients with poor clinical compliance.

Design outcomes

Primary

MeasureTime frame
objective response rate;disease control rate;

Secondary

MeasureTime frame
progression-free survival;Tumor downstaging rate;Surgical conversion rate;Adverse events;

Countries

China

Contacts

Public ContactJun Zhu

The Second People's Hospital of Yibin

865149749@qq.com+86 138 9096 0428

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026