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Effect of donor characteristics on T cell replete haploidentical stem cell transplantation

Effect of donor characteristics on T cell replete haploidentical stem cell transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052233
Enrollment
Unknown
Registered
2021-10-23
Start date
2008-03-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Hematological malignancies

Interventions

case series:none

Sponsors

The First Affiliated Hospital of Medical College of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The subjects or their legal representatives signed the informed consent before the clinical study. 2. Subjects aged 8 to 65 years. 3. Patients have no suitable HLA identical sibling donor. 4. Patients with malignant hematological diseases plan to receive peripheral blood stem cell donor source T cell replete haoloidentical stem cell transplantation. 5. Patients with ECoG score of 0-2. 6. Patients who received myeloablative conditioning regimen treatment. 7. Accepting anti-T-lymphocyte globin(ATG) based GVHD prophylaxis.

Exclusion criteria

Exclusion criteria: 1. Patients have suitable HLA identical sibling donor. 2. Patients with severe liver and kidney function (alanine aminotransferase > 2.5 times of the upper normal limit, serum creatinine > 1.5 times of the upper normal limit), cardiopulmonary dysfunction (cardiac function NYHA III / IV, cardiac ejection fraction < 50%, severe obstructive or restrictive ventilation dysfunction). 3. Patients with active infection. 4. Patients diagnosed with aplastic anemia before transplantation. 5. Patients with secondary tumor. 6. Patients who received reduced-intensity conditioning treatment. 7. Patients who received a second transplant. 8. Patients who cannot independently choose to enter or exit clinical trials due to serious central nervous system disease or mental disease.

Design outcomes

Primary

MeasureTime frame
Overall Survival;incidence of graft versus host disease;

Secondary

MeasureTime frame
non-relapses mortality;disease-free survival;incidence of relapse;

Countries

China

Contacts

Public ContactHuang He

The First Affiliated Hospital of Medical College of Zhejiang University

hehuangyu@126.com+86 13605714822

Outcome results

None listed

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