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Clinical Trials/NCT03171831
NCT03171831
Unknown
Phase 4

Haploidentical Hematopoietic Stem Cell Transplantation for Patients With Thalassemia Major

First Affiliated Hospital of Guangxi Medical University1 site in 1 country30 target enrollmentApril 1, 2017

Overview

Phase
Phase 4
Intervention
Busulfan
Conditions
Thalassemia Major
Sponsor
First Affiliated Hospital of Guangxi Medical University
Enrollment
30
Locations
1
Primary Endpoint
Overall Survival
Last Updated
8 years ago

Overview

Brief Summary

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

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
April 1, 2017
End Date
April 1, 2022
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
First Affiliated Hospital of Guangxi Medical University
Responsible Party
Principal Investigator
Principal Investigator

Yongrong Lai

Director of the Hematology Department

First Affiliated Hospital of Guangxi Medical University

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

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

Arms & Interventions

Haploidentical HSCT

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)

Intervention: Busulfan

Haploidentical HSCT

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)

Intervention: Cyclophosphamide

Haploidentical HSCT

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)

Intervention: Fludarabine

Haploidentical HSCT

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)

Intervention: Mycophenolate mofetil

Haploidentical HSCT

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)

Intervention: Tacrolimus

Haploidentical HSCT

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)

Intervention: Methotrexate

Haploidentical HSCT

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)

Intervention: Thymoglobulin

Haploidentical HSCT

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)

Intervention: Basiliximab

Outcomes

Primary Outcomes

Overall Survival

Time Frame: 2 years

2-years overall survival

Secondary Outcomes

  • 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)

Study Sites (1)

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