Allo-hematopoietic stem cell transplantation(HSCT) is the only way to cure β-thalassemia major at present. To expand donor pool,we developed a haplo-identical HSCT (Hi-HSCT) platform. But in prior Hi-HSCT using high dose post-transplant Cyclophosphamide in patients with leukemia, cytopenia post-transplant often developed, which was considered as a symptom of GVHD. Therefore, the investigators add unrelated umbilical cord blood (UCB) to the Hi-HSCT. It has reported that, as third-party cells, UCB will reduce GVHD.The purpose of this study is to determine whether unrelated UCB following Hi-HSCT can improve outcomes of Hi-HSCT in patients with β-thalassemia major.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Department of paediatrics,Nangfang Hospital, Southern Medical University
Guangzhou, Guangdong, China
RECRUITINGoverall survival(OS)
the measure is a composite
Time frame: 12 months
TM-free survival(TFS)
the measure is a composite
Time frame: 12 months
Transplant Related Martality (TRM)
the measure is a composite
Time frame: 12 months
Primary or Secondary Graft Rejection (GR)
the measure is a composite
Time frame: 12 months
The cumulative incidences of acute graft-versus-host disease(GVHD)
the measure is a composite
Time frame: 12 months
The cumulative incidences of chronic graft vesus host disease (cGVHD)
the measure is a composite
Time frame: 12 months
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