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Effect of PD-1 /PD-L1 Inhibitor Therapy Before Liver Transplantation on Acute Rejection After Liver Transplantation in Patients With Hepatocellular Carcinoma

B

Beijing Tsinghua Chang Gung Hospital

Status

Unknown

Conditions

Hepatocellular Carcinoma
Acute Rejection

Study type

Observational

Funder types

Other

Identifiers

NCT05411926
21299-4-03

Details and patient eligibility

About

This study is a single-center, prospective, non-interventional cohort study based on the real world data.In this study, 30 patients with a history of PD-1/PD-L1 monotherapy prior to liver transplantation and 30 patients without a history of PD-1/PD-L1 monotherapy prior to liver transplantation were recruited from the group of patients with hepatocellular carcinoma who had undergone allogeneic liver transplantation.Collected patient data included demographics, oncology and immunotherapy history, evaluated index before liver transplantation, laboratory, pathological and imaging results at specific time points after transplantation (1 week, 2 weeks, 3 weeks, 4 weeks, 12 weeks, 16 weeks, 24 weeks), as well as the occurrence of acute rejection (AR) , grading of severity, and anti-rejection treatment plan at the same time. Endpoints included relapse-free survival and overall survival (OS). These data aims to assess: 1) the incidence of acute rejection after liver transplantation in patients with hepatocellular carcinoma; 2) the time of acute rejection, Banff classification, and acute rejection-related mortality after liver transplantation in patients with hepatocellular carcinoma; 3) the cellular immune function after liver transplantation;; 4) the dose and drug concentration of tacrolimus after liver transplantation in patients with hepatocellular carcinoma; and 5) the overall survival (OS) and relapse-free survival(RFS) after liver transplantation in patients with hepatocellular carcinoma.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. age between 18 and 70 years,
  2. Eastern Cooperative Oncology Group (ECOG) performance score ≤3,
  3. voluntarily participate, totally understand in the study and sign the Informed Consent Form (ICF),
  4. hepatopathology confirmed hepatocellular carcinoma after liver transplantation, 5)patients with hepatocellular carcinoma treated with PD1/PD-L1 monoclonal antibody prior to liver transplantation,

6)PD-1/PD-L1 monotherapy needs to be used ≥ 2 times (The patients were divided into observation and control group according to whether received PD-1/PD-L1 monoclonal antibody treatment before liver transplantation)

Exclusion criteria

  1. patients with incomplete clinicopathological data,
  2. post-transplantation ≥6months,
  3. PD-1/PD-L1 monotherapy required for oncological reasons after liver transplantation.

Trial design

30 participants in 2 patient groups

The group that receiving PD-1 / PD-L1 inhibitor before liver transplantation
The group without receiving PD-1 / PD-L1 inhibitor before liver transplantation

Trial contacts and locations

1

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Central trial contact

Rui Tang, Ph.D

Data sourced from clinicaltrials.gov

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