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Efficacy and safety of radiofrequency ablation combined with local immunity and antivascular therapy for advanced liver cancer

Efficacy and safety of radiofrequency ablation combined with local immunity and antivascular therapy for advanced liver cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035162
Enrollment
Unknown
Registered
2020-08-02
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

liver cancer

Interventions

Case series:Radiofrequency ablation of liver lesions
Local immune drug PD-1 was injected into liver lesions
Oral administration of the antivascular-targeting drug Eitan

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) 18-75 years old; (2) HCC was confirmed by pathological examination; (3) Liver lesions that can be assessed by imaging; (4) BCLC stage: B-C; (4) Child-pugh classification: A-B; (5) ECOG PS: 0-2 marks; (6) Previous or no HCC treatment; (7) Sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Contraindications to radiofrequency ablation; (2) A history of allergy to PD-1 antibody; (3) HIV positive; (4) The presence of autoimmune diseases; (5) With a severe infection or serious underlying disease, such as hemorrhagic peptic ulcer, ileus, heart failure, renal failure or poorly controlled diabetes; (6) Failure to comply with the test requirements; (7) Pregnancy (confirmed by serum or urine human chorionic gonadotropin [-HCG]) or lactation.

Design outcomes

Primary

MeasureTime frame
OS;lesions size;

Countries

China

Contacts

Public ContactWeixi Shen

The Second Affliated Hospital of Harbin Medical University

Shenweixi1982@163.com+86 15776659232

Outcome results

None listed

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