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Safety and Efficacy Study of Photopheresis With UVADEX to Prevent Graft-versus-Host Disease

Primary Purpose

Graft-versus-Host Disease

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Methoxsalen
Extracorporeal Photopheresis
Sponsored by
Mallinckrodt
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Graft-versus-Host Disease focused on measuring Extracorporeal Photopheresis, Graft-versus-Host Disease

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with a diagnosis of a malignancy of the blood (e.g. leukemia) for which allogeneic bone marrow or peripheral blood stem cell transplantation is a treatment option. Patients who are candidates for a standard allogenic bone marrow transplant or PBSC transplant. Patients must have adequate renal, hepatic, pulmonary and cardiac function to enable the patient to tolerate shifts in the volumes of body fluids associated with extracorporeal photopheresis, as determined by the physician's clinical judgement. Patients must weigh at least 40 kg (88 lbs) Exclusion Criteria: Patients who have received a prior bone marrow transplant or peripheral blood stem cell transplant.

Sites / Locations

  • University of Florida
  • University of Chicago
  • Tufts New England Medical Center
  • Kansas City Cancer Center
  • Cleveland Clinic Foundation
  • Texas Transplant
  • Royal Brisbane Hospital
  • Peter MacCallum Cancer Institute
  • Alfred Hospital
  • Royal Melbourne Hospital
  • St. Vincent's Hospital
  • Hospital Azevedo Carvalho
  • National Cancer Institute
  • Hemocentro
  • Ludwig-Maximiliano Universitaet Muenchen
  • Careggi Hospital
  • San Martino Hospital
  • Instituto Portugues de Oncologia de Francisco Gentil
  • National Cancer Institute
  • Ankara University Medical School
  • Hammersmith Hospital

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
February 5, 2003
Last Updated
August 14, 2017
Sponsor
Mallinckrodt
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1. Study Identification

Unique Protocol Identification Number
NCT00054600
Brief Title
Safety and Efficacy Study of Photopheresis With UVADEX to Prevent Graft-versus-Host Disease
Official Title
A Study of Extracorporeal Photopheresis With UVADEX in the Setting of a Standard Myeloablative Conditioning Regimen for the Prevention of Graft-versus-Host Disease in Patients Undergoing an Allogeneic Bone Marrow Transplant or Peripheral Blood Stem Cell Transplant
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
June 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2004 (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mallinckrodt

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether Extracorporeal Photopheresis with UVADEX (ECP) prior to bone marrow or peripheral blood stem cell transplantation is effective in the prevention of Graft-versus-Host Disease (GvHD).
Detailed Description
Approximately 30% of HLA-identical related bone marrow graft recipients and up to 90% of patients receiving bone marrow from unrelated donors develop significant acute GvHD despite the use of prophylactic therapies such as cyclosporine and methotrexate. About half of these patients respond to initial treatment with steroids and require no further treatment. The remainder of these patients are either unresponsive to initial therapy or become steroid-resistant over time. The prognosis in these cases is poor and mortality for patients with steroid-resistant GvHD may be as high as 50%. ECP is a technique in which peripheral white blood cells are exposed to a photoactivatable compound (UVADEX) administered extracorporeally and ultraviolet A light. After cells are reinfused into the patient, their function is altered, thereby activating mechanisms that allow for further regulation of specific lymphocyte populations. ECP has shown activity in several inflammatory and autoimmune diseases, including scleroderma, rheumatoid arthritis, transplantation rejection, acute and chronic GvHD. In a previous single-center, open label, single-arm study of 56 patients receiving ECP treatment on two consecutive days and reduced-intensity bone-marrow conditioning prior to bone marrow transplantation from matched or partially matched human donors, the incidence of grade II-IV acute GvHD was less than 10%. This is in contrast to an expected incidence of approximately 40%. The purpose of this study is to determine the role of ECP, administered pre-transplant, in preventing GvHD when used in conjunction with a standard myeloablative conditioning regimen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft-versus-Host Disease
Keywords
Extracorporeal Photopheresis, Graft-versus-Host Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Methoxsalen
Intervention Type
Procedure
Intervention Name(s)
Extracorporeal Photopheresis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a diagnosis of a malignancy of the blood (e.g. leukemia) for which allogeneic bone marrow or peripheral blood stem cell transplantation is a treatment option. Patients who are candidates for a standard allogenic bone marrow transplant or PBSC transplant. Patients must have adequate renal, hepatic, pulmonary and cardiac function to enable the patient to tolerate shifts in the volumes of body fluids associated with extracorporeal photopheresis, as determined by the physician's clinical judgement. Patients must weigh at least 40 kg (88 lbs) Exclusion Criteria: Patients who have received a prior bone marrow transplant or peripheral blood stem cell transplant.
Facility Information:
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32611
Country
United States
Facility Name
University of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Tufts New England Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Kansas City Cancer Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
Texas Transplant
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Royal Brisbane Hospital
City
Brisbane
ZIP/Postal Code
4006
Country
Australia
Facility Name
Peter MacCallum Cancer Institute
City
East Melbourne
ZIP/Postal Code
8006
Country
Australia
Facility Name
Alfred Hospital
City
Melbourne
Country
Australia
Facility Name
Royal Melbourne Hospital
City
Parkville
ZIP/Postal Code
3050
Country
Australia
Facility Name
St. Vincent's Hospital
City
Sydney
ZIP/Postal Code
2010
Country
Australia
Facility Name
Hospital Azevedo Carvalho
City
Jau
Country
Brazil
Facility Name
National Cancer Institute
City
Rio de Janeiro
Country
Brazil
Facility Name
Hemocentro
City
Sao Paulo
Country
Brazil
Facility Name
Ludwig-Maximiliano Universitaet Muenchen
City
Munchen
ZIP/Postal Code
D-81377
Country
Germany
Facility Name
Careggi Hospital
City
Florence
ZIP/Postal Code
1-50134
Country
Italy
Facility Name
San Martino Hospital
City
Genova
ZIP/Postal Code
16132
Country
Italy
Facility Name
Instituto Portugues de Oncologia de Francisco Gentil
City
Lisbon
ZIP/Postal Code
1099-023
Country
Portugal
Facility Name
National Cancer Institute
City
Bratislava
Country
Slovakia
Facility Name
Ankara University Medical School
City
Ankara
ZIP/Postal Code
6100
Country
Turkey
Facility Name
Hammersmith Hospital
City
London
ZIP/Postal Code
W12 0NN
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
10411505
Citation
Shlomchik WD, Couzens MS, Tang CB, McNiff J, Robert ME, Liu J, Shlomchik MJ, Emerson SG. Prevention of graft versus host disease by inactivation of host antigen-presenting cells. Science. 1999 Jul 16;285(5426):412-5. doi: 10.1126/science.285.5426.412.
Results Reference
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Safety and Efficacy Study of Photopheresis With UVADEX to Prevent Graft-versus-Host Disease

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