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The study of interventional therapy combined with target immunotherapy for unresectable Hepatocellular Carcinoma

The study of interventional therapy combined with target immunotherapy for unresectable Hepatocellular Carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083936
Enrollment
Unknown
Registered
2024-05-08
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-13

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:Interventional therapy combined with target immunotherapy

Sponsors

Dongying People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the clinical diagnostic criteria of the 2022 Guidelines for the Diagnosis and Treatment of Primary Liver Cancer or are pathologically diagnosed with primary liver cancer, have at least one measurable tumor lesion, and are not suitable for/refuse to undergo surgical resection; 2. Gender unlimited, 18-75 years old; 3. CNLC Ib-IIIb; 4. Child-Pugh A-B ; 5. ECOG 0-1; 6. No serious complications; 7. The patient's expected survival was more than 3 months; 8. Agree to participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Huge liver tumor (=60% liver volume); 2. Patients with diffuse liver cancer; 3. unstable systemic disease or uncontrolled infection; 4. Dysfunction of renal function and coagulation that is difficult to correct; 5. Bleeding from esophageal or fundus varices caused by portal hypertension in the past 6 months, or any life-threatening bleeding event within 3 months; 6. Any unstable condition or condition that may compromise the patient's safety and his/her compliance with the study; 7. Any adverse events that require termination of treatment; 8. The patient or legal representative requests that treatment be discontinued; 9. Unable to complete the treatment plan for various reasons, or the patient lost follow-up; 10. The investigator considered other patients not suitable to participate in this study

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Overall survival;Objective response rate;Disease control rate;

Countries

China

Contacts

Public ContactBo Yuan

Dongying People's Hospital

xx8359@163.com+86 136 9546 7415

Outcome results

None listed

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