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Cryopreservation of White Blood Cells Before Their UVA Irradiation for Graft Versus Host Disease Treatment (cryo-ECP)

Primary Purpose

Graft Versus Host Disease

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cryopreservation
Sponsored by
Central Hospital, Nancy, France
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Graft Versus Host Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Adult or child who received an allogeneic hematopoietic stem cell transplantation, with a medical follow-up at the University Hospital of Nancy, or at the other University Hospitals in the great East region (Dijon, Reims, Besançon) in which ECP is not accessible.
  • Eligible for ECP for the treatment of acute or chronic steroid refractory GVHD, after pluridisciplinary concertations
  • Patients (or parents) who received full information on the research and who signed a consent for this research

Non inclusion Criteria:

  • Children under 10 kg of weight
  • Patients or parents who did not sign a consent
  • Patients who present an absolute contra-indication for apheresis: recent pulmonary embolism, deep vein thrombosis, myocardial infarction, active and evolutive bacterial or fungal infection, hemodynamics instability, deep anemia (Hb < 8g/dl) or deep thrombocytopenia (< 20 g/L) despite transfusions, severe hypocalcemia.
  • Women in age to procreate without contraception

Sites / Locations

    Outcomes

    Primary Outcome Measures

    intensity of ECP regimen
    Number of ECP (fresh and thawed) sessions during 3 months

    Secondary Outcome Measures

    systemic infections during 3 months after cryo-ECP (safety)
    occurrence of death after cryo-ECP (safety)
    occurrence of relapse of the initial hematological disease after cryo-ECP (safety)
    Steroid sparing effect (efficacy)
    GVHD grade (severity) (efficacy)
    immunosuppressive drugs used (efficacy)

    Full Information

    First Posted
    November 22, 2017
    Last Updated
    January 23, 2020
    Sponsor
    Central Hospital, Nancy, France
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03361254
    Brief Title
    Cryopreservation of White Blood Cells Before Their UVA Irradiation for Graft Versus Host Disease Treatment
    Acronym
    cryo-ECP
    Official Title
    Division and Cryopreservation of Autologous Blood Nuclear Cells for Intensive Regimen of Extracorporeal Photopheresis : Interest for the Treatment of Patients With Steroid Resistant Graft Versus Host Disease
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 31, 2020 (Anticipated)
    Primary Completion Date
    June 30, 2020 (Anticipated)
    Study Completion Date
    September 30, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Central Hospital, Nancy, France

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No

    5. Study Description

    Brief Summary
    Extracorporeal photopheresis (ECP) is a worldwide recognized treatment of acute and chronic mild to moderate graft versus host disease (GVHD), in second or further line of treatment. Contrary to immunosuppressive drugs, ECP is not associated with side effects such as opportunistic infections, and is not associated with a higher frequency of relapse of the initial hematological disease. High intensity of ECP regimen (1 to 3 sessions per week, in case of chronic or acute GVHD) seems to be correlated to a higher efficacy. However, high intensity of ECP treatment is often difficult to sustain, because of frequent logistical problems to perform aphereses, such as venous access failure, infections of central line, deep blood cytopenias that require many transfusions before performing aphereses. Merlin et al. first described the feasibility of white blood cells cryopreservation before UVA irradiation, in vitro, then in vivo. We also recently reported the feasibility and efficacy of cryopreserved ECP in a series of 20 patients (adults and children), with acute and chronic GVHD, who had recurrent contraindications to aphereses, that prevented the realization of an intensive program of ECP. No adverse events occurred, and efficacy seemed to be similar to "classical" ECP (35% of complete overall response, and 40% of partial response). White blood cells (WBC) were divided after collection on Optia or Cellex apheresis machines: one was immediately treated with 8-MOP (methoxsalen) and ultraviolet A (UVA) irradiation, while the other was cryopreserved, and further (a few days later) thawed, sensitized with 8-MOP and irradiated before injection to the patient. The aim of this study is to analyze this method in a prospective way, with complete biological data collection, of apoptosis, cytokines release etc…, necessary to the full description of cryopreservation of white blood cells before their irradiation and reinjection to the patient. We will propose this technique of cryopreservation to every patient with an indication of ECP for acute or chronic GVHD in Nancy Hospital for 18 months.
    Detailed Description
    The main objective of this prospective interventional pilot study is to demonstrate the ability of this technique to follow high intensity regimen recommendations, as mentioned above: 3 ECP sessions (thawed or fresh) per week during 3 months for grade III to IV acute GVHD, then 2 ECP sessions (thawed or fresh) per week during 3 months for grade II acute GVHD 1 ECP session per week for chronic GVHD during 3 months The other objectives are: To describe the safety and efficacy of cryo ECP. Efficacy will be assessed with a composite criteria test, comporting 5 items, which will be compared for each patient with a paired cohort of historical patients treated in Nancy University Hospital since 2010 (match will be made on type and grade of GVHD, and age under and over 18 year-old) To fully describe the biological consequences of cryopreservation of WBC before UVA irradiation: apoptosis rate and time, lymphocyte functional tests (lymphoblastic transformation test), cytokines release, number of lymphocytes, and monocytes at the time of reinjection, bacteriological tests, residual diméthylsulfoxyde (DMSO) quantification To demonstrate the decrease in red blood cells and platelets transfusion number, due to the sparing effect of cryo ECP on aphereses number.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Graft Versus Host Disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    demonstrate the ability of this technique to follow high intensity regimen recommendations
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    5 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Biological
    Intervention Name(s)
    cryopreservation
    Intervention Description
    cryopreservation to every patient with an indication of ECP for acute or chronic GVHD in Nancy Hospital for 18 months
    Primary Outcome Measure Information:
    Title
    intensity of ECP regimen
    Description
    Number of ECP (fresh and thawed) sessions during 3 months
    Time Frame
    3 months after the first ECP session
    Secondary Outcome Measure Information:
    Title
    systemic infections during 3 months after cryo-ECP (safety)
    Time Frame
    at 6 weeks and 3 months after the first ECP session
    Title
    occurrence of death after cryo-ECP (safety)
    Time Frame
    at 6 weeks and 3 months after the first ECP session
    Title
    occurrence of relapse of the initial hematological disease after cryo-ECP (safety)
    Time Frame
    at 6 weeks and 3 months after the first ECP session
    Title
    Steroid sparing effect (efficacy)
    Time Frame
    at 6 weeks and 3 months after the first ECP session
    Title
    GVHD grade (severity) (efficacy)
    Time Frame
    at 6 weeks and 3 months after the first ECP session
    Title
    immunosuppressive drugs used (efficacy)
    Time Frame
    at 6 weeks and 3 months after the first ECP session

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adult or child who received an allogeneic hematopoietic stem cell transplantation, with a medical follow-up at the University Hospital of Nancy, or at the other University Hospitals in the great East region (Dijon, Reims, Besançon) in which ECP is not accessible. Eligible for ECP for the treatment of acute or chronic steroid refractory GVHD, after pluridisciplinary concertations Patients (or parents) who received full information on the research and who signed a consent for this research Non inclusion Criteria: Children under 10 kg of weight Patients or parents who did not sign a consent Patients who present an absolute contra-indication for apheresis: recent pulmonary embolism, deep vein thrombosis, myocardial infarction, active and evolutive bacterial or fungal infection, hemodynamics instability, deep anemia (Hb < 8g/dl) or deep thrombocytopenia (< 20 g/L) despite transfusions, severe hypocalcemia. Women in age to procreate without contraception
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Cécile POCHON, Dr.
    Phone
    00 33 3 83 15 46 28
    Email
    c.pochon@chru-nancy.fr

    12. IPD Sharing Statement

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    Cryopreservation of White Blood Cells Before Their UVA Irradiation for Graft Versus Host Disease Treatment

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