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临床试验/NCT03171831
NCT03171831Unknown4 期

Haploidentical Hematopoietic Stem Cell Transplantation for Patients With Thalassemia Major

First Affiliated Hospital of Guangxi Medical University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
30
试验地点
1
主要终点
Overall Survival

研究概览

简要总结

The purpose of the study is to assess the safety and efficacy of haploidentical hematopoietic stem cell transplantation for patients with thalassemia major.

详细描述

The only curative therapy for thalassemia major remains the replacement of the defective erythropoiesis by allogeneic hematopoietic stem cell transplantation(HSCT). However, this option is unavailable to many patients as a result of a lack of compatible donors.Haploidentical transplantation has been certified as a valuable alternative for hematological malignancy patients lacking a well-matched donor, with results comparable matched HLA-identical sibling donors or unrelated donors.The objective of this study is to test the feasibility of haploidentical HSCT for patients with thalassemia major.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with thalassemia major
  • Lacking of a HLA-identical sibling donor or unrelated donor
  • Indication of haploidentical hematopoietic stem cell transplantation
  • No restrictions for transplantation

排除标准

  • Any restriction for transplantation
  • No indication of haploidentical hematopoietic stem cell transplantation

研究组 & 干预措施

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Busulfan (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Cyclophosphamide (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Fludarabine (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Mycophenolate mofetil (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Tacrolimus (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Methotrexate (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Thymoglobulin (Drug)

Haploidentical HSCT

Experimental

Procedure: Haploidentical hematopoietic stem cell transplantation from a related donor (partially matched sibling, father or mother).

Conditioning: Busulfan (4 mg/kg/day,4 days) + Cyclophosphamide (50 mg/kg/day,4 days)+ Fludarabine (50 mg/m2/day,3 days)

GVHD Prophylaxis:Mycophenolate mofetil(0.25g/day)+ Tacrolimus(0.03mg/kg/day)+ Methotrexate(15mg/m2 on day +1,10mg/m2 on day +3,+6,+11)+ Thymoglobulin(2.5 mg/kg/day,4 days)+Basiliximab(10mg on day 0 and +4)

干预措施: Basiliximab (Drug)

结局指标

主要结局

Overall Survival

时间窗: 2 years

2-years overall survival

次要结局

  • Disease Free Survival(2 years)
  • Engraftment(30 days)
  • Transplant Related Mortality(1 year)
  • Cumulative Incidence of acute Graft Versus Host Disease(180 days)
  • Cumulative Incidence of chronic Graft Versus Host Disease(2 years)
  • Cumulative Incidence of Infectious Complications(2 years)

研究者

发起方
First Affiliated Hospital of Guangxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yongrong Lai

Director of the Hematology Department

First Affiliated Hospital of Guangxi Medical University

研究点 (1)

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