In recent years, the curative effect of AML has been greatly improved. However, 20% - 30% of young patients and 40% - 50% of old patients will relapse again. Its re induction response rate is low, the survival period is short, and the prognosis is very poor. At present, there is no standard treatment scheme. Although a small number of patients can benefit from allogeneic hematopoietic stem cell transplantation (allo HSCT), most patients lack suitable donors. The choice of high-dose chemotherapy is a rescue treatment scheme, but the treatment-related hematology or non hematology related toxicity and high mortality make the scheme controversial, especially for the elderly. Some studies have proposed a new treatment method combining chemotherapy with peripheral blood hematopoietic stem cell infusion after mobilization of HLA mismatched donors. Preliminary clinical studies verified that after more than 70 cases of elderly acute myeloid leukemia were treated with microtransplantation, the complete remission rate reached 80%, the 2-year disease-free survival rate reached 39%, the early mortality rate was only 6.7%, and the median recovery time of neutrophils and platelets was 11 and 14.5 days, respectively, which was significantly different from the control group of chemotherapy alone. After that, the micro transplantation technology was extended to the treatment of myelodysplastic syndrome and lymphoma, and good results were also obtained. Compared with peripheral blood / bone marrow hematopoietic stem cells, umbilical cord blood (UCB) hematopoietic stem cells have the advantages of rapid access, convenient source, no harm to donors, and low requirements for HLA matching. The immune cells in cord blood hematopoietic stem cells are mostly Na ï ve and immature immune cells, so the incidence and severity of graft-versus-host disease (GVHD) after unrelated cord blood transplantation are low, which not only reduces the failure of transplantation due to GVHD, but also avoids a series of complications and high costs brought by complex GVHD prevention and treatment techniques. Because cord blood is rich in CD16 + CD56 + NK cells and CD3 + T cells, cord blood hematopoietic stem cell transplantation also plays an important role in GVL.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
57
The basic chemotherapy regimen was the same as that of the control group UCB micro transplantation scheme: Aza 100mg, 75mg/m2/d, IVGTT, D-10 to D-4 Ara-C 1000mg/m2/q12h, IVGTT, D-3 to D-2 Single non consanguineous umbilical cord blood (NC \> 1.5 \* 10 \^ 7 / kg), IVGTT, D0 Bone marrow aspiration smear, MRD and bone marrow chimerism were detected on D14, d30 and D60 after transplantation.
Zhongnan Hospital of Wuhan University
Wuhan, Hubei, China
RECRUITINGChange from marrow blast in percentage at Week 18
marrow blast in percentage
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from Blood routine in plasma at Week 18
WBC
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from Blood routine in plasma at Week 18
RBC
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from Blood routine in plasma at Week 18
PLT
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from liver and kidney function at Week 18
ALB
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from liver and kidney function at Week 18
GLB
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from liver and kidney function at Week 18
eGFR
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
ECG QT Interval,ST segment,P wave,QPS wave group
We will record this index in the first day
Time frame: Day 1
Change from Blood routine in plasma at Week 18
Hb
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from liver and kidney function at Week 18
Creatine
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
Change from liver and kidney function at Week 18
β2-MG
Time frame: Day 0,Day 1,Week 1,Week4,Week 12,Week 18
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