Overview
Risk Stratification Directed Conditioning Regimen for Haploidentical HSCT in SAA
Status:
Recruiting
Recruiting
Trial end date:
2022-03-30
2022-03-30
Target enrollment:
0
0
Participant gender:
All
All
Summary
The haplotype HSCT system including Bu(0.8mg/kg Q6hx2d)CTX(50mg/kgx4d)rATG(2.5mg/kgx4d) , established in Institute of Hematology of Peking University ,has been evaluated to be effective for acquired SAA.But some patients with high risk factors may not tolerate CTX 200mg/kg,alternative conditioning regimen including Bu/Fludarabine/dercreased CTX was studied in this trial.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Peking University People's HospitalTreatments:
Busulfan
Cyclophosphamide
Fludarabine
Fludarabine phosphate
Thymoglobulin
Criteria
A:inclusion criteria1. Patients diagnosed as acquired severe aplastic anemia(SAA) /very vSAA
2. patients with age 3-55 years
3. patients have no matched sibling donor
4. Patients have no matched unrelated donor
5. patients have no severe infection
6. Patients have no severe organ dysfunction
7. patients have risk factors of potential intolerance to previous condition regimen
including BuCy(200mg/kg)and ATG
8. Consent form signed
B. Exclusion criteria :
1. patients with congenital SAA/vSAA
2. patients with age< 3years or >55 years
3. patients with matched sibling donor
4. patients with matched URD
5. patients with severe infection
6. patients with severe organ dysfunction
7. pregnancy women
8. no Consent form signed