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
About this trial
This is an interventional treatment trial for Graft Versus Host Disease
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
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
NCT ID
NCT03361254
First Posted
November 22, 2017
Last Updated
January 23, 2020
Sponsor
Central Hospital, Nancy, France
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
Learn more about this trial
Cryopreservation of White Blood Cells Before Their UVA Irradiation for Graft Versus Host Disease Treatment
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