Study of biomarkers in liver cancer after surgery
Official title: Biomarkers and Molecular Mechanism Study of Hepatocellular Carcinoma After Radical Resection and Conversion Therapy
Run by Shanghai Zhongshan Hospital · NCT06382103 · Data updated 2026-11-12
This study looks at blood samples from liver cancer patients who had surgery to see if certain markers can help predict their long-term health and guide their treatment.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | Shanghai Zhongshan Hospital Academic / other |
| Locations | 1 site (Shanghai) |
| Status | Recruiting |
| Started | May 15, 2024 |
| Main results expected | May 20, 2025 |
| Study ends | May 20, 2026 |
| Registry record updated | March 26, 2025 |
| Trial ID | NCT06382103 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients with a first diagnosis of hepatocellular carcinoma who are scheduled for surgical treatment.
✕Probably not a fit
Patients with secondary liver cancer, intrahepatic cholangiocarcinoma, or other concurrent malignancies may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to analyze blood samples from patients with hepatocellular carcinoma (HCC) who have undergone surgical resection. It focuses on identifying circulating tumor DNA (ctDNA) and plasma protein levels to enhance the prediction of long-term prognosis and inform treatment options. By monitoring ctDNA and conducting plasma proteomic analysis, the study seeks to improve patient outcomes following surgery. The findings could lead to more personalized treatment strategies for HCC patients.
Why it matters
Potential benefit: If successful, this study could provide more accurate prognostic information and tailored treatment options for patients with hepatocellular carcinoma.
How similar studies have gone: Other studies have shown promise in using ctDNA and plasma proteomics for cancer prognosis, indicating a potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with a first diagnosis of HCC. * Patients with HCC who are to undergo surgical treatment, with or without neoadjuvant therapy. * Ability to obtain tissue sample for ctDNA analysis and detectable baseline ctDNA level. Exclusion Criteria: * Patients with secondary liver cancer, or intrahepatic cholangiocarcinoma. * Any other concurrent malignancy. * History of organ transplant or hepatic encephalopathy.
Where it's running
-
Zhongshan Hospital Fudan University
Shanghai, China Recruiting
Study contacts
- Study coordinator: Huichuan Sun
- Email: sun.huichuan@zs-hospital.sh.cn
- Phone: +86-21-64041990
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.