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Kinectics of Donor-specific Anti-HLA Antibody After HLA-incompatible Allogeneic Haematopoietic Stem Cell Transplantation

Recruiting
Conditions
Haematological Malignancy
Registration Number
NCT06395220
Lead Sponsor
Peking University People's Hospital
Brief Summary

Donor specific anti-HLA antibody (DSA) is closely related not only to primary graft rejection (GR) after HLA-incompatible transplantation, but also to the occurrence of primary PGF. Desensitisation therapy can reduce the level of DSA in patients and decrease the incidence of PGF after transplantation. However, most studies at home and abroad have focused on DSA levels in recipients before transplantation, risk factors and their effects on prognosis. Very few studies have focused on the rate of DSA positivity and its risk factors after transplantation. Therefore, this project aims to clarify the rate of DSA positivity after HLA-incompatible Allo-HSCT and reveal the influencing factors of post-transplantation DSA positivity with the help of a prospective, registry-based clinical cohort of HLA-incompatible transplant recipients, in order to provide a basis for the prevention and treatment of DSA-induced graft rejection or PGF.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
800
Inclusion Criteria

Clinical diagnosis haematological disorders undergoing HLA-incompatible allogeneic haematopoietic stem cell transplantation Between 15 and 60 years-old Must sign the informed consent

Exclusion Criteria

Withdraw of the signed informed consent for any reason Lack of ability to provide consent due to psychiatric or physical illness

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Positive rates of post-transplantation donor-specific anti-HLA antibody (DSA).through study completion, an average of 2 years

HLA-A, -B, -C, -DRB1, -DQB1, and -DPB1 alleles were determined according to the literatures published by our group \[Huo MR, et al. Bone Marrow Transplant. 2018;53(5):600-608\].

Secondary Outcome Measures
NameTimeMethod
Acute graft-versus-host disease (aGVHD)2 years

Acute GVHD was defined and graded from I to IV based on the pattern and severity of organ involvement \[Sullivan KM. Graft-versus-host-disease. In: Thomas ED, Blume KG, Forman SJ (eds). Hematopoietic Cell Transplantation. 5nd edn. Blackwell Science: Boston, MA, USA, 2020, pp 515-536.\].

Chronic graft-versus-host disease (cGVHD)2 years

Chronic GVHD was defined and graded according to the National Institute of Health criteria:\[Biol Blood Marrow Transplant,2005,11: 945\] that is, mild cGVHD reflects the involvement of no more than 1 or 2 organs/sites (except for lung) with a maximum score of 1; moderate cGVHD involves at least 1 organ/site with a score of 2 or ≥3 organs/sites with a score of 1 (or lung score 1); and severe cGVHD is diagnosed when a score of 3 is given to any organ (or lung score 2). The diagnosis is mainly based on clinical manifestations.

Cumulative incidence of relapse2 years

Relapse was defined by the morphological evidence of disease in the peripheral blood, BM or extramedullary sites. Time to relapse was defined from the date of transplantation to the date of disease recurrence. Patients exhibiting minimal residual disease (for example, the presence of BCR/ABL RNA transcripts by PCR) were not classified as having morphological relapse.

Non-relaspe mortality (NRM)2 years

Non-relapse mortality was defined as all causes of death other than those related directly to malignant disease itself, occurring at any time after transplantation.

Neutrophil engraftment2 years

Neutrophil engraftment was defined as the first day of an absolute neutrophil count above 0.5×109/L for three consecutive days after the neutrophil nadir.

Platelet engraftment2 years

Platelet engraftment was defined as the first of 7 consecutive days during which the platelet count was at least 20×109/L without needing transfusion.

Primary graft failure2 years

Primary graft failure was defined as never achieved an ANC \>0.5×109/L for thress consecutive days or an ANC \>0.5×109/L without donor engraftment (autologous recovery).

Secondary graft-failurefunction2 years

Secondary graft-failure was defined as decline or loss of donor engraftment.

Disease-free survival (LFS)2 years

Disease-free survival was defined as days from transplantation to disease progression after transplantation.

Overall survival (OS)2 years

Overall survival referred to patients who survived until the final follow-up time point.

Trial Locations

Locations (1)

People's Hospital of Peking University

🇨🇳

Beijing, China

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