Effect of Donor Chose on the Outcomes of GVHD Prophylaxis Underwent the Combined Treatment of ATG/PTCy for Haplo-HSCT

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-55
SponsorShanghai General Hospital, Shanghai Jiao Tong University School of Medicine

About this trial

This is a prospective, multicenter, cohort study. The high-risk, relapse and refractory AML patients were enrolled in this study. And the goal of this study is to study the effect of the parous female donor and young male donor on the outcomes of graft-versus-host disease (GVHD) prophylaxis underwent the combination of ATG and PTCy for haploidentical peripheral blood stem cell transplantation

Eligibility criteria

Qualifiers

ELN prognostic stratification high-risk group (see Appendix for criteria)

Non-remission (NR) AML: including primary refractory AML and NR patients after relapse.

Patients had to have a qualified haploidentical young male (≤30 years old) or female with a history of pregnancy;

Related donors had to be related donors matched 5/10-7/10 for HLA-A, -B, -C, -DQB1 and -DRB1 3. All the enrolled patients received a unified GVHD prevention regimen based on ATG and PTCy

Disqualifiers

Intermediate-low risk AML patients (ELN criteria);

Patients with extramedullary active lesions at the time of transplantation;

Haploidentical collateral donors;

Patients who refused allogeneic hematopoietic stem cell transplantation;

Trial design

Treatments tested in this trial

  • None-placebo
  • non-intervention study
  • donor selection

Treatment groups

No treatment groups listed

Locations

This trial has no locations