Safety and Efficacy Study of Photopheresis With UVADEX to Prevent Graft-versus-Host Disease
- Conditions
- Graft-versus-Host Disease
- Registration Number
- NCT00054600
- Lead Sponsor
- Mallinckrodt
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- 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)
- Patients who have received a prior bone marrow transplant or peripheral blood stem cell transplant.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (20)
Tufts New England Medical Center
๐บ๐ธBoston, Massachusetts, United States
University of Chicago
๐บ๐ธChicago, Illinois, United States
Kansas City Cancer Center
๐บ๐ธKansas City, Missouri, United States
Cleveland Clinic Foundation
๐บ๐ธCleveland, Ohio, United States
Texas Transplant
๐บ๐ธSan Antonio, Texas, United States
Royal Brisbane Hospital
๐ฆ๐บBrisbane, Australia
Peter MacCallum Cancer Institute
๐ฆ๐บEast Melbourne, Australia
Alfred Hospital
๐ฆ๐บMelbourne, Australia
Royal Melbourne Hospital
๐ฆ๐บParkville, Australia
St. Vincent's Hospital
๐ฆ๐บSydney, Australia
Hospital Azevedo Carvalho
๐ง๐ทJau, Brazil
Hemocentro
๐ง๐ทSao Paulo, Brazil
Ludwig-Maximiliano Universitaet Muenchen
๐ฉ๐ชMunchen, Germany
San Martino Hospital
๐ฎ๐นGenova, Italy
Hammersmith Hospital
๐ฌ๐งLondon, United Kingdom
University of Florida
๐บ๐ธGainesville, Florida, United States
National Cancer Institute
๐ธ๐ฐBratislava, Slovakia
Instituto Portugues de Oncologia de Francisco Gentil
๐ต๐นLisbon, Portugal
Ankara University Medical School
๐น๐ทAnkara, Turkey
Careggi Hospital
๐ฎ๐นFlorence, Italy