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

Sponsor
Beijing Tsinghua Chang Gung Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05411926
Collaborator
(none)
30
1
29.5
1

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Effect of PD-1 /PD-L1 Inhibitor Therapy Before Liver Transplantation on Acute Rejection After Liver Transplantation in Patients With Hepatocellular Carcinoma
    Actual Study Start Date :
    Mar 17, 2021
    Anticipated Primary Completion Date :
    Mar 1, 2023
    Anticipated Study Completion Date :
    Sep 1, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    The group that receiving PD-1 / PD-L1 inhibitor before liver transplantation

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

    Outcome Measures

    Primary Outcome Measures

    1. 1) the incidence of acute rejection after liver transplantation in patients with hepatocellular carcinoma; [2021-03~2023-03]

    2. 2) the severity of acute rejection after liver transplantation in patients with hepatocellular carcinoma; [2021-03~2023-03]

    3. 3) the cellular immune function after liver transplantation,including lymphocyte subsets and cytokines [2021-03~2023-03]

    4. 4) the dose and drug concentration of tacrolimus after liver transplantation in patients with hepatocellular carcinoma; [2021-03~2023-03]

    Secondary Outcome Measures

    1. 5) the overall survival (OS) and relapse-free survival(RFS) after liver transplantation in patients with hepatocellular carcinoma. [2021-03~2023-03]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Tsinghua Changgung Hospital Beijing Beijing China 102218

    Sponsors and Collaborators

    • Beijing Tsinghua Chang Gung Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Beijing Tsinghua Chang Gung Hospital
    ClinicalTrials.gov Identifier:
    NCT05411926
    Other Study ID Numbers:
    • 21299-4-03
    First Posted:
    Jun 9, 2022
    Last Update Posted:
    Jun 9, 2022
    Last Verified:
    Mar 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 9, 2022