Comparison of clinical outcomes between unrelated single umbilical cord blood and "ex-vivo" T-cell depleted haploidentical transplantation in children with hematological malignancies

被引:2
|
作者
Gomez-Santos, Carmen [1 ]
Gonzalez-Vicent, Marta [1 ]
Molina, Blanca [1 ]
Deltoro, Natalia [1 ]
Herrero, Blanca [1 ]
Ruiz, Julia [1 ]
Perez-Martinez, Antonio [1 ,2 ]
Diaz, Miguel A. [1 ]
机构
[1] Hosp Infantil Univ Nino Jesus, Hematopoiet Stem Cell Transplantat Unit, Dept Pediat, Menedez Pelayo 65, Madrid 28009, Spain
[2] Hosp Infantil Univ La Paz Madrid, Madrid, Spain
关键词
Children; Cord blood transplant; Hematologic malignancies; Immune reconstitution; TCD haploidentical transplant; VERSUS-HOST-DISEASE; HEMATOPOIETIC STEM-CELLS; IMMUNE RECONSTITUTION; ACUTE-LEUKEMIA; ALTERNATIVE DONORS; GRAFTS; ADULTS; IMPACT; MANIFESTATIONS; DIAGNOSIS;
D O I
10.1007/s12519-021-00461-w
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background Over the last two decades, umbilical cord blood (UCB) and haploidentical transplantation (HaploHSCT) have emerged as alternative sources of hematopoietic stem cell for allogeneic transplantation. There are few retrospective studies and no prospective studies comparing both types of alternative transplantation in pediatric patients. Results We analyzed the data of 134 children with hematological malignancies who received a hematopoietic stem cell transplantation from a single umbilical cord blood (UCB) (n = 42) or an "ex-vivo" T-cell depleted transplant from a haploidentical-related donor (HaploHSCT) (n = 92) between 1996 and 2014. Hematological recovery was faster after HaploHSCT than the UCB transplant group (median times to neutrophil and platelet recovery: 13 vs. 16 days, 10 vs. 57 days, respectively) (P < 0.001). The HaploHSCT group had a significantly early immune reconstitution based on NK and CD8 + T cells compared with the UCB group. However, after the first year post-transplantation, HaploHSCT had a lower number of CD4 + T and B lymphocytes compared with the UCB transplant recipients. The cumulative incidence of TRM was 29 +/- 8% in the HaploHSCT group versus 40 +/- 5% in the UCB group. Relapse incidence was 21 +/- 7% in the HaploHSCT group and 19 +/- 8% in the UCB group. Probability of DFS was 58 +/- 8% in the HaploHSCT group versus 40 +/- 9% in the UCB group (P = 0.051). Conclusions TCD haploidentical transplant is associated with advantages in terms of engraftment and early immune reconstitution kinetics. TCD haploidentical transplant was associated with lower incidence of infectious and non-infectious complications, especially in the early phases of the transplant compared with UCB transplant recipients. However, there are no advantages in transplant outcomes compared with UCB transplant.
引用
收藏
页码:609 / 618
页数:10
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