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ABO Blood Type Incompatibility Is Not a Risk Factor of Outcomes for Acute Myeloid Leukemia (AML) Patients After Unmanipulated Haplo-Identical Peripheral Blood Hematopoietic Stem Cell Transplantation
被引:3
|作者:
Yang, Nan
[1
]
Guan, Lixun
[1
]
Liu, Zhanxiang
[1
]
Ding, Yi
[1
]
Zhu, Chengying
[1
]
Luo, Lan
[1
]
Wang, Feiyan
[1
]
Fang, Shu
[1
]
Gao, Zhe
[1
]
Gu, Zhenyang
[1
]
Gao, Chunji
[1
]
机构:
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Hematol, Beijing, Peoples R China
基金:
北京市自然科学基金;
关键词:
Blood Group Incompatibility;
Haploidy;
Hematopoietic Stem Cell Transplantation;
Leukemia;
Myeloid;
Acute;
HEMATOLOGIC MALIGNANCIES;
IMPACT;
DONOR;
MISMATCH;
MORTALITY;
D O I:
10.12659/AOT.916004
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Background: Haplo-identical hematopoietic stem cell transplantation (HSCT) has provided potential donors for patients lacking available HLA-matched donors. ABO blood type compatibility has been reported to be associated with HSCT outcomes. However, few studies have investigated the role of ABO compatibility in haplo-identical HSCT of AML patients. Material/Methods: We retrospectively analyzed 42 adult acute myeloid leukemia (AML) patients who received unmanipulated haplo-identical peripheral blood HSCT at the Chinese PLA General Hospital between Jan 2013 and Dec 2017. We analyzed the role of ABO compatibility in engraftment, transfusion requirements, cytomegalovirus (CMV) and Epstein-Barr virus (EBV) viremia, acute graft-versus-host disease (GVHD), overall survival (OS), transplantation-related mortality (TRM), relapse, chronic GVHD, and post-transplant lymphoproliferative disorder (PTLD). Results: There were no significant differences between the ABO-matched group and the ABO-mismatched group in terms of engraftment, transfusion requirements, CMV and EBV viremia, OS, TRM, relapse, PTLD, and chronic GVHD. Univariate analysis revealed ABO incompatibility is not an independent risk factor of engraftment, transfusion requirements, CMV and EBV viremia, OS, TRM, relapse, PTLD, and chronic GVHD. We found a significantly higher cumulative incidence of aGVHD in the matched group compared with the mismatched group (80.95% vs. 42.86%, p=0.020). In multivariate analysis, ABO mismatch was associated with decreased risk of acute GVHD within 100 days after transplant (hazard ratio 0.492, 95% confidence interval 0.2123-1.14). However, the difference was not statistically significant (p=0.099). Conclusions: This study demonstrated ABO incompatibility is not an independent risk factor of outcomes for AML patients who received unmanipulated haplo-identical peripheral blood HSCT. ABO compatibility might have limited value in haplo-identical donor selection.
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页码:350 / 358
页数:9
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