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Mechanisms of Tumorigenesis and Recurrence Metastasis under Immunosuppression Post Organ Transplantation and the Establishment of Precision Diagnosis and Treatment Strategies (Subproject 1: Early Warning System for De Novo Tumors under Immunosuppression Post Organ Transplantation) Clinical Research

Mechanisms of Tumorigenesis and Recurrence Metastasis under Immunosuppression Post Organ Transplantation and the Establishment of Precision Diagnosis and Treatment Strategies (Subproject 1: Early Warning System for De Novo Tumors under Immunosuppression Post Organ Transplantation) Clinical Research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099624
Enrollment
Unknown
Registered
2025-03-26
Start date
2023-12-12
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

De Novo and Recurrent Tumors Post Organ Transplantation

Interventions

De Novo and Recurrent Tumors Post Organ Transplantation:Does not involve

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Retrospective Study: Patients who underwent allogeneic renal transplantation at West China Hospital of Sichuan University between 2015 and 2023, aged over 18 and under 65 years, regardless of gender, will be included. Additionally, data will be collected on patients who developed de novo tumors post-renal transplantation between 2015 and 2023, along with a matched control cohort. Prospective Study: Patients who will undergo allogeneic renal transplantation from deceased donors at West China Hospital of Sichuan University between 2024 and 2026, aged between 18 and 65 years, will be prospectively enrolled.

Exclusion criteria

Exclusion criteria: 1 Recipients with a history of malignancy; 2 Kidney transplant recipients whose donor relatives have a history of malignancy; 3 Recipients with ABO blood type incompatibility; 4 Recipients with active hepatitis B or hepatitis C (positive HBV-DNA or HCV-RNA in blood).

Design outcomes

Primary

MeasureTime frame
Patient basic information;Test results;Imaging results;Pathology examination results;Medication Treatment Plan;

Countries

China

Contacts

Public ContactLin Tao

West China Hospital of Sichuan University

Kidney5@163.com+86 189 8060 2093

Outcome results

None listed

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