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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05411926
Other study ID # 21299-4-03
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 17, 2021
Est. completion date September 2023

Study information

Verified date March 2022
Source Beijing Tsinghua Chang Gung Hospital
Contact Rui Tang, Ph.D
Phone 13811337617
Email tangrui_hs@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date September 2023
Est. primary completion date March 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility 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.

Study Design


Locations

Country Name City State
China Beijing Tsinghua Changgung Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Tsinghua Chang Gung Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 1) the incidence of acute rejection after liver transplantation in patients with hepatocellular carcinoma; 2021-03~2023-03
Primary 2) the severity of acute rejection after liver transplantation in patients with hepatocellular carcinoma; 2021-03~2023-03
Primary 3) the cellular immune function after liver transplantation,including lymphocyte subsets and cytokines 2021-03~2023-03
Primary 4) the dose and drug concentration of tacrolimus after liver transplantation in patients with hepatocellular carcinoma; 2021-03~2023-03
Secondary 5) the overall survival (OS) and relapse-free survival(RFS) after liver transplantation in patients with hepatocellular carcinoma. 2021-03~2023-03
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