A Study of CD147-targeted CAR-T by Hepatic Artery Infusions for Very Advanced Hepatocellular Carcinoma

August 24, 2019 updated by: Chen Zhinan, Xijing Hospital

An Open-label, Dose Escalation Clinical Study to Access the Safety and Clinical Activity of CD147-targeted CART by Hepatic Artery Infusions for Very Advanced Hepatocellular Carcinoma

This is a single-center, single-arm, open label and dose escalation clinical study of anti-CD147 CART cells by hepatic artery infusions in patients with advanced hepatocellular carcinoma.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Patients autologous T cells are activated and then engineered to express chimeric antigen receptors (CARs) specific for CD147(CD147-CART). CAR-T cells are expanded in culture and returned to the patient by hepatic artery infusion at specific cell doses. Four CD147-CART doses patient are planned at 1-week intervals. Tumor biopsies will be obtained at the time of the initial diagnostic angiogram and during the first infusion session. Serum cytokine level and CAR-T cell number will be measured in whole treatment session.

Study Type

Interventional

Enrollment (Anticipated)

34

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • China
    • Shaanxi
      • Xi'an, Shaanxi, China, 710032
        • Recruiting
        • Department of hepato-biliary & Pancreato Splenic Surgery Organ Transplant Center, Xijing Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Age ≥ 18 year and ≤ 65 years, both male and female.
  2. Advanced hepatocellular carcinoma(HCC) patient, which is untreatable by surgery or local therapy, or has postoperative progressions, failed at least one and two line of standard systemic chemotherapy, and unwilling or intolerance to targeting therapy or immune-therapy of cancer.
  3. The portal vein is not total occlusion, or collateral circulation has formed between hepatic artery and blocked portal vein.
  4. Patient with measurable HCC focus defined by mRECIST.
  5. Patient with histologically confirmed diagnosis of CD147+ hepatocellular carcinoma.
  6. Adequate venous access for apheresis, and no other contraindications for apheresis.
  7. Child-Pugh score ≤7.
  8. Eastern Cooperative Oncology Group(ECOG) performance status of 0-2.
  9. Patient with a life expectancy of greater than three months.
  10. Patients must able to understand and be willing to sign an informed consent.

Exclusion Criteria:

  1. Patients with fibrolamellar carcinoma of liver，mixed hepatocellular carcinoma or cholangiocarcinoma.
  2. Patients with severe hypohepatia including jaundice, hepatic encephalopathy, refractory ascites or hepatorenal syndrome.

  3. Patients with severe comorbidity, including any of the following.

    1. Unstable angina pectoris and/or congestive heart failure need hospitalization;
    2. Myocardial infarction or cerebrovascular accident (CVA) in the last 6 months;
    3. chronic obstructive pulmonary disease progressions or need hospitalization;
    4. severe cardiovascular, nervous system, hematological, gastrointestinal, endocrine diseases or metabolic disorders;
    5. autoimmune disease or immunodeficiency disease;
    6. acute bacterial infections or fungal infections needs intravenous injection of antibiotics during CAR-T cell therapy;
    7. tuberculosis not cured;
    8. other malignancies;
  4. Patients who have received gene therapy, cell therapy or immune therapy.
  5. Patients who have received organ transplantation.
  6. Patients who have received treatment of targeted drugs, glucocorticoid or immunosuppressive drugs within 2 weeks before enrolling in clinical trial.
  7. Patients who have received chemotherapy except for lymphocyte clearance within 2 weeks before enrolling in clinical trial.
  8. Patients who have received radiotherapy.
  9. Patients who did not recover to CTCAE(v5.0) grade 1 from adverse events （except hair）of previous anti-tumor therapy before enrolling in trial.
  10. Syphilis test (TRUST) positive, Anti-HIV positive, Anti-HCV positive with HCV-RNA level higher than the lower limit of detection(LOD), or HBcAb positive with HBV-DNA level higher than the LOD.

  11. Patients with following abnormalities:

    1. Absolute neutrophil count (ANC) < 1.5E9/L, platelet(PLT) < 50E9/L, or hemoglobin(HGB)< 80 g/dL;
    2. Prothrombin time (PT), activated partial thromboplastin time (APTT) or international normalized ratio (INR) > 1.5×ULN (upper normal value);
    3. Total bilirubin(TBIL) > 2×ULN; ALT, AST or ALP>5×ULN;
    4. Serum creatinine (Cr)≥1.5×ULN or glomerular filtration rate (GFR) < 60 mL/min·1.73m^2;
    5. left ventricular ejection fraction (LVEF) < 50%;
  12. Patients with a history of allergic reactions attributed to any agents or compounds involved in this study.
  13. Patients with a history of mental disorders.
  14. Patients with a history of drug abuse.
  15. Pregnant and lactating women.
  16. Patients of childbearing age who unwilling or unable to take birth control from during this study and 3 months post this study.
  17. Patients who receive any other investigational agents within the 3 months before enrolling in this clinical trial.
  18. Investigator considers not suitable for this trial.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: CD147-CART
Infusions of CD147-CART cells over the course of each week for 3 times into the hepatic artery
Biological: CD147-CART
Three infusions of CD147-CART cells over the course of three weeks into the hepatic artery.
Other Names:
  • anti-CD147 chimeric antigen receptor T cell

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence and type of adverse events induced by CD147-CART hepatic artery infusions
Time Frame: 12 weeks
To assess the safety of CD147-CART (anti-CD147 CAR-T cell) hepatic artery infusions (HAI) for very advanced hepatocellular carcinoma which measured by number and type of adverse events.
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
DLT and MTD of CD147-CART cell hepatic artery infusions
Time Frame: 12 weeks
To determine the dose limited toxicity (DLT) and maximum tolerated dose (MTD) of CD147-CART hepatic artery infusions.
12 weeks
Activity of CD147-CART cell hepatic artery infusions
Time Frame: 2 years
To evaluate treatment response of CD147-CART hepatic artery infusions for very advanced hepatocellular carcinoma.
2 years
CD147-CART detection in extrahepatic sites
Time Frame: 2 years
Quantification of CD147-CART cells in blood samples.
2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Xijing Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 27, 2019

Primary Completion (ANTICIPATED)

October 27, 2020

Study Completion (ANTICIPATED)

May 27, 2022

Study Registration Dates

First Submitted

June 19, 2019

First Submitted That Met QC Criteria

June 19, 2019

First Posted (ACTUAL)

June 21, 2019

Study Record Updates

Last Update Posted (ACTUAL)

August 28, 2019

Last Update Submitted That Met QC Criteria

August 24, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Chen Zhinan-1

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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