PTCy-ATG vs ATG in Haploidentical HSCT for Acute Graft-versus-host Disease Prophylaxis
Hematopoietic Stem Cell Transplantation
About this trial
This is an interventional prevention trial for Hematopoietic Stem Cell Transplantation focused on measuring Hematopoietic Stem Cell Transplantation, posttransplantation cyclophosphamide, antithymocyte globulin, viral infection, graft-versus-host disease
Eligibility Criteria
Inclusion Criteria:
- A patient age of 18-65 years
- Haploidentical hematopoietic stem cell transplant recipient
- Subjects (or their legally acceptable representatives) must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study
Exclusion Criteria:
- Any abnormality in a vital sign (e.g., heart rate, respiratory rate, or blood pressure)
- Patients with any conditions not suitable for the trial (investigators' decision)
Sites / Locations
- Department of Hematology,Nanfang Hospital, Southern Medical UniversityRecruiting
- Guangzhou First People's Hospital
- Sun Yat-sen Memorial Hospital, Sun Yat-sen University
- The Third Affiliated Hospital, Sun Yat-Sen University
- Xiangya Hospital, Central South University
- Chenzhou First People's Hospital
- Peking University People's Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
PTCy-ATG group
ATG group
PTCy-ATG group refers to treatment with PTCy-ATG protocol as GVHD prophylaxis at a total dose of 4.5mg/kg ATG, a dose of 50mg/kg/d cyclophosphamide (CTX), a dose of 2.5mg/kg/d Ciclosporin A (CsA), and a dose of 1.0g/d Mycophenolate Mofetil(MMF).
ATG group refers to treatment with ATG protocol as GVHD prophylaxis at a total dose of 7.5mg/kg ATG, a dose of 2.5mg/kg/d Ciclosporin A (CsA), a dose of 1.0g/d Mycophenolate Mofetil(MMF) and methotrexate (MTX, on days +1, +3 and +6).