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Radiofrequency ablation combined with recombinant human type-5 adenovirus and PD-1 monoclonal antibody for the treatment of small hepatocellular carcinoma:A prospective cohort study

Radiofrequency ablation combined with recombinant human type-5 adenovirus and PD-1 monoclonal antibody for the treatment of small hepatocellular carcinoma:A prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118841
Enrollment
Unknown
Registered
2026-02-11
Start date
2025-01-15
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

hepatocellular carcinoma

Interventions

Radiofrequency ablation combined with recombinant human type-5 adenovirus and PD-1 monoclonal antibodies for treatment group:None
RFA-only treatment group:None

Sponsors

The 958th Hospital of Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed as primary hepatocellular carcinoma, using pathological examination as the standard or referring to the diagnostic criteria of the Chinese Liver Cancer Diagnosis and Treatment Guidelines (2023 edition); 2.Age range: 18-75 years old; 3.Single tumor with a diameter of <= 5cm; 4.Have not received H101 treatment or regular use of PD-1 monoclonal antibody treatment in the past; 5.The tumor has not invaded the secondary or lower branches of the hepatic artery, portal vein, or hepatic vein; 6.The patient's liver function is classified as Child A or Child B and reaches Child A after treatment; 7.Important organ function can tolerate RFA, without contraindications related to oncolytic virus therapy and PD-1 monoclonal antibody therapy.

Exclusion criteria

Exclusion criteria: 1.Receive other anti-tumor treatments or liver transplantation during the trial period; 2.Patients with extrahepatic metastasis, lymph node metastasis, or concomitant tumors of other systems; 3.Child C liver function, Child B liver function that cannot be improved by treatment; 4.Severe coagulation dysfunction: platelet count4 seconds or international normalized ratio INR>1.5; 5.Cases of combined refractory ascites, hepatic encephalopathy, and gastrointestinal bleeding; 6.ECOG physical status score >= 2; 7.Patients who have lost follow-up.

Design outcomes

Secondary

MeasureTime frame
Complete ablation rate;Ablation range;complications;hospital stay;

Primary

MeasureTime frame
recurrence-free survival rates;overall survival rates;local tumor progression rates;Alpha fetoprotein levels;

Countries

China

Contacts

Public ContactWu Guodong

The 958th Hospital of Army

evans30337@163.com+86 134 5236 0006

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026