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Impact of donor-recipient ABO incompatibility on patients' outcome after peripheral blood stem cell haploidentical stem cell transplantation.

Impact of donor-recipient ABO matching on patients' outcome after peripheral blood stem cell haploidentical stem cell transplantation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052232
Enrollment
Unknown
Registered
2021-10-23
Start date
2013-01-01
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 malignacies

Interventions

ABO matched:none
Minor incompatibility:none
Major incompatibility:none
Bidirectional incompatibility:none

Sponsors

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

Eligibility

Sex/Gender
All
Age
10 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.The subjects or their legal representatives signed the informed consent before the clinical study. 2.Patients aged 10 to 70 years. 3.Patients with malignant hematological diseases plan to receive allogeneic peripheral blood stem cell transplantation 4.Patients have no suitable HLA identical sibling donor 5.Patients with malignant hematological diseases plan to receive HLA haploidentical stem cell transplantation 6.Patients with ECoG score of 0-2.

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 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;

Secondary

MeasureTime frame
Non-relapse mortality;incidence of graft versus host disease; neutrophils engraftment;platelets engraftment;blood transfusion requirements;blood transfusion independence;the incidence of poor graft function;the incidence of graft failure;

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