NCT07379489Not yet recruiting
Adjuvant Anti-PD-1 Therapy in Resected Hepatocellular Carcinoma
Efficacy of Postoperative Adjuvant PD-1 Inhibitors Guided by a Deep Learning Model: a Multicenter, Prospective Cohort Study
Source: ClinicalTrials.gov · Last updated 30 Jan 2026
Brief summary (registry, in English)
Early hepatocellular carcinoma (HCC) recurrence (driven by residual tumors) and late recurrence (driven by de novo tumors) exhibit distinct biological behaviors, suggesting differential therapeutic vulnerabilities. The beneficiaries of adjuvant PD-1 inhibitors (aPD-1) and their efficacy across these temporally divergent recurrence patterns remains unestablished.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 300 (estimated)
- First submitted
- 23 Jan 2026
- Start date
- 31 Jan 2026
- Primary completion date
- 31 Dec 2029
- Lead sponsor
- Tongji Hospital
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT07379489
What you commit to
- Study type: Observational
- Planned participants: 300
- From 31 Jan 2026 to the primary completion date, 31 Dec 2029
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- prior treatments for HCC;
- received other adjuvant therapy.
Other illness
- history of other malignancies or recurrent HCC;
- mixed or other types of liver cancer;
Other
- extrahepatic metastasis;
- ongoing severe postoperative complications;
Who the study is looking for
- Aged between 18 and 75;
- achieved complete tumor resection;
- histological verification of HCC;
- liver function classified as Child-Pugh grade A or B;
- No other serious systemic disease or organ dysfunction.
Age in the registry: 18 years to 75 years · Sex: All
This page is information, not medical advice. Discuss any trial with your doctor.