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Multicenter clinical research of related HLA-haploidentical/mismatched allogeneic non T cell-depleted in vitro peripheral blood hematopoietic stem cell transplantation for hematologic malignance

Multicenter clinical research of related HLA-haploidentical/mismatched allogeneic non T cell-depleted in vitro peripheral blood hematopoietic stem cell transplantation for hematologic malignance

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-15006663
Enrollment
Unknown
Registered
2015-06-29
Start date
2015-07-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hematologic malignance

Interventions

Case series:Related HLA-haploidentical/mismatched allogeneic non T cell-depleted in vitro peripheral blood hematopoietic stem cell transplantation

Sponsors

Hematologic disease center,First Affiliated Hospital of XinJiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1) Age: 15 to 50 years old; 2) Confirmed diagnosis hematological malignancies, including: ALL in initial treatment (standard risk and high risk group), AML in initial treatment?except M3 (moderated and high risk group), MDS (IPSS up 3.5), recurrence of refractory ALL and AML(note: use a IPSS MDS - R scoring system); 3) HLA-matching all used high resolution genotyping and choose 2/6 or 3/6 HLA-halpltype (HLA - A, B and DRB1); 4) Patiens haven't severely organ injury of heart, lung, kidney, only mild damage to liver function (Child class A); 5) The following feasible transplantation: patients with hepatitis b virsus, hepatitis c virsus of not actively liver damage and strict monitoring viral replication in normal copy number; with TB infection of infected has been control, under continue to anti-TB treatment; patients have?fungal infection?recently of full control of infected site; 6) All volunteer signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) There is difficult to control the active infection; 2) Patients have organ injury of heart, lung, kidney and severe liver damage (Child class B, C); 3) Pregnancy; 4) Mental illness; 5) Patients don't sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Acute graft versus host disease;

Secondary

MeasureTime frame
Chronic graft versus host disease;Engraftment;Overall Surviver;disease free survival;transplantation related mortality;

Countries

China

Contacts

Public ContactMing Jiang
jiangmingyy@126.com+86 13609910116

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026