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Mechanisms of tumor recurrence and metastasis post-liver transplantation for HCC

Mechanisms of tumor recurrence and metastasis post-liver transplantation for HCC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102399
Enrollment
Unknown
Registered
2025-05-14
Start date
2024-12-09
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

After Liver Transplantation for Hepatocellular Carcinoma

Interventions

The recurrence group after liver transplantation for hepatocellular carcinoma:None
The non-recurrence group after liver transplantation for hepatocellular carcinoma:None

Sponsors

The Third Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Recurrence Group: Patients who meet the Hangzhou criteria for liver transplantation for hepatocellular carcinoma (HCC); Patients with pathologically confirmed recurrence and metastasis more than six months after surgery; Patients who have not undergone antitumor chemotherapy or interventional therapy but may have received preventive targeted therapy; Patients who understand and sign the informed consent form. 2.Non-Recurrence Group: Patients who have no recurrence or metastasis for more than two years after surgery; Patients who may have received targeted therapy for recurrence prevention are also eligible; Patients who understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1). Patients who develop new tumors after surgery.;(2) Patients with a history of or currently concurrent other malignant tumors;(3) Patients with hepatocellular carcinoma (HCC) who experience recurrence or death within 3 months after liver transplantation; (4) Patients with abnormal liver or kidney function at present; (5) Patients who have undergone combined transplantation of multiple organs, such as the liver and kidney;(6) Patients with active tuberculosis infection; (7) Patients who are human immunodeficiency virus (HIV) positive;(8) Patients with a history of alcohol consumption, or consumption of probiotics or prebiotics within 1 week before sampling;patients who have undergone colonoscopy, intestinal enema treatment, or received antibiotic or traditional Chinese medicine treatment within 1 week before sampling; (9) Other factors that, in the judgment of the investigator, may affect the safety or compliance of the participant.

Design outcomes

Primary

MeasureTime frame
Intestinal microbiota;

Countries

China

Contacts

Public ContactShuhong Yi

The Third Affiliated Hospital Sun Yat-sen University

yishh@mail.sysu.edu.cn+86 20 82179626

Outcome results

None listed

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