Acute graft-versus-host disease (aGVHD) is a potentially fatal complication after allogeneic hematopoietic cell transplantation (HCT), particularly for that with a HLA-mismatched donor. Abatacept has been demonstrated as a potent drug to reduce the risk of aGVHD, but the efficacy of subcutaneous form has yet been investigated. This trial is designed to preliminarily determin the efficacy and saftey of subcutaneous abatacept in the prevention of aGVHD after haplo-identical HCT.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
29
subcutaneous abatacept: 250mg (d-1) , 125mg (d+5, +14, +21, +28, +35, +42, +49, +56) combined with CsA, MTX, MMF.
the First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China
RECRUITINGIncidence of overt aGVHD
The incidence of grade II-IV aGVHD post-transplantation
Time frame: 100 days post-HCT
Incidence of aGVHD
The incidence of grade I-IV aGVHD post-transplantation
Time frame: 100 days post-HCT
Incidence of severe aGVHD
The incidence of grade III-IV aGVHD post-transplantation
Time frame: 100 days post-HCT
Early transplant-related mortality
The incidence of early transplant-related mortality
Time frame: 100 days post-HCT
Relapse
The incidence of relapse/progression of underlying disease
Time frame: 100 days post-HCT
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