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Hepatic Artery Infusion of CD34+ Cells

Primary Purpose

Stem Cell Transplantation, Liver Diseases

Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Hepatic artery infusion of CD34+ cells
Cobe Spectra
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stem Cell Transplantation focused on measuring Severe hepatic dysfunction post stem cell transplantation, Stem Cell Transplantation, Hepatic Artery Infusion, Liver Diseases, CD34+ Cells, SCT

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: SCT recipients with severe hepatic dysfunction (bilirubin equal to or greater than 5mg/dl) and histologically documented VOD. The original stem cell donor must be sex-mismatched, willing and able to donate G-CSF-mobilized peripheral blood stem cells. The patient must have complete donor chimerism. Exclusion Criteria: Patients who do not have at least 5 x 10^6 donor CD34+ cells/kg available for infusion. Patients with graft versus host disease (GVHD). Patients in whom hepatic artery infusion cannot be performed because of anatomical or technical reasons. Patients with active hepatitis B or C.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Hepatic Artery Infusion

    Arm Description

    Donor-derived CD34+ cells administered in a total volume of 100ml via hepatic artery over 10 minutes. Cells given as a dose escalation study. First cohort of 3 patients receive 1 * 106 CD34+ cells/kg. Next 3 patients receive 2.5 * 106 CD34+cells/kg. Next 3 patients receive 5 * 106 CD34+ cells/kg. Less than 1 * 105 T cells/kg administered.

    Outcomes

    Primary Outcome Measures

    Learn if donor's cells can produce liver cells when injected directly into the liver and whether this procedure will improve liver function and survival.

    Secondary Outcome Measures

    Full Information

    First Posted
    June 9, 2003
    Last Updated
    October 25, 2018
    Sponsor
    M.D. Anderson Cancer Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00062543
    Brief Title
    Hepatic Artery Infusion of CD34+ Cells
    Official Title
    Hepatic Artery Infusion of CD34+ Cells, Isolated by the Isolex 300i Device, in Stem Cell Transplant Recipients With Hepatic Failure Due to Veno-occlusive Disease
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2018
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    May 2002 (undefined)
    Primary Completion Date
    October 2005 (Actual)
    Study Completion Date
    October 2005 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    M.D. Anderson Cancer Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary objective is to determine whether donor stem cells administered via hepatic artery infusion can produce liver cells in patients with severe hepatic dysfunction post stem cell transplantation (SCT) and the safety of this procedure. The secondary objective is to improve liver function and improve survival.
    Detailed Description
    Participants in this study have received stem cell transplantation. As a result of this procedure, participants have developed severe liver dysfunction. Researchers have recently discovered that cells circulating in the blood and bone marrow are capable of forming liver cells. Before taking part in this study, women able to have children must have a negative blood pregnancy test. Participants in this study will have donor's cells infused directly into their liver through a catheter that will be inserted through the groin. This will be done after liver disease has been diagnosed by liver biopsy. The catheter will stay in the groin for no more than 3 days. During that time, participants will be exposed to repeated x-ray exams to ensure that the catheter stays in place. During the time that the catheter is in place, the infusion will be repeated as long as donor's cells are available. Participants will receive different drugs by vein to decrease the risk of transfusion reaction. After completing donor cell infusion, the catheter will be removed. After participants are released from the hospital, they will have periodic evaluation of liver size. About 1 teaspoon of blood will be drawn for standard blood tests to evaluate liver function. Around Days 28 and 90, participants will have liver biopsy. This is an investigational study. A total of 10 patients will take part in this study. All will be enrolled at UTMDACC.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Stem Cell Transplantation, Liver Diseases
    Keywords
    Severe hepatic dysfunction post stem cell transplantation, Stem Cell Transplantation, Hepatic Artery Infusion, Liver Diseases, CD34+ Cells, SCT

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Hepatic Artery Infusion
    Arm Type
    Experimental
    Arm Description
    Donor-derived CD34+ cells administered in a total volume of 100ml via hepatic artery over 10 minutes. Cells given as a dose escalation study. First cohort of 3 patients receive 1 * 106 CD34+ cells/kg. Next 3 patients receive 2.5 * 106 CD34+cells/kg. Next 3 patients receive 5 * 106 CD34+ cells/kg. Less than 1 * 105 T cells/kg administered.
    Intervention Type
    Procedure
    Intervention Name(s)
    Hepatic artery infusion of CD34+ cells
    Intervention Description
    Donor's cells infused directly into liver through a groin catheter (hepatic artery).
    Intervention Type
    Device
    Intervention Name(s)
    Cobe Spectra
    Other Intervention Name(s)
    blood cell separator
    Intervention Description
    Mononuclear cells (MNC) collected by continuous-flow centrifugation using a blood cell separator (Cobe Spectra).
    Primary Outcome Measure Information:
    Title
    Learn if donor's cells can produce liver cells when injected directly into the liver and whether this procedure will improve liver function and survival.
    Time Frame
    3 Years

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: SCT recipients with severe hepatic dysfunction (bilirubin equal to or greater than 5mg/dl) and histologically documented VOD. The original stem cell donor must be sex-mismatched, willing and able to donate G-CSF-mobilized peripheral blood stem cells. The patient must have complete donor chimerism. Exclusion Criteria: Patients who do not have at least 5 x 10^6 donor CD34+ cells/kg available for infusion. Patients with graft versus host disease (GVHD). Patients in whom hepatic artery infusion cannot be performed because of anatomical or technical reasons. Patients with active hepatitis B or C.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Zeev Estrov, MD
    Organizational Affiliation
    M.D. Anderson Cancer Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Links:
    URL
    http://www.mdanderson.org
    Description
    UT MD Anderson Cancer Center website

    Learn more about this trial

    Hepatic Artery Infusion of CD34+ Cells

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