The purpose of this study is to assess preliminary efficacy and to determine the safety and feasibility of ex vivo generated dendritic cell (HDC) infusion with and without donor lymphocyte infusion (DLI) after allogeneic stem cell transplant (SCT). We also wish to establish the feasibility of apheresis shipment as well as vaccine shipment and stability in the population.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Patients who have minimal residual disease or minimal volume relapse, and are at least four weeks post immunosuppression following allogeneic stem cell transplantation will receive a series of four HDC infusions (100,000 HDC/kg per infusion, one every four weeks(group 1). Those patients who have greater than minimal residual disease will receive HDC infusions, one every four weeks in conjunction with donor lymphocyte infusion (DLI) (group 2).
Mount Sinai Medical Center
New York, New York, United States
RECRUITINGThe incidence of severe graft versus host disease (GVHD) grade C or D as defined by IBMTR grading.
Time frame: 2 weeks following each HDC infusion and 4, 6 and 8 weeks after the last HDC infusion
The incidence of grade A and B acute GVHD, limited chronic GVHD, infusion reactions, graft loss and donor chimerism
Time frame: 2 weeks following each HDC infusion and 4, 6 and 8 weeks after the last HDC infusion
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.