Haploidentical vs. HLA-matched donor hematopoietic stem-cell transplantation for pediatric patients with acute lymphoblastic leukemia in second remission: A collaborative retrospective study of the Spanish Group for Bone Marrow Transplantation in Children (GETMON/GETH) and the Spanish Childhood Relapsed ALL Board (ReALLNet)

Other authors

Institut Català de la Salut

[Moreno C, Ramos-Elbal E] Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain. [Velasco P, Díaz de Heredia C] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Aguilar Y] Hospital Universitario Miguel Servet, Zaragoza, Spain. [Gonzáález Martínez B] Hospital Universitario La Paz, IdiPAZ, Instituto de Investigación, Hospital Universitario La Paz, Madrid, Spain. [Fuentes C] Hospital Universitario y Politécnico La Fe, Valencia, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2023-04-26T11:40:35Z

2023-04-26T11:40:35Z

2023-03-20

Abstract

Acute lymphoblastic leukemia; Children; Stem cell transplantation


Leucemia linfoblástica aguda; Niños; Trasplante de células madre


Leucèmia limfoblàstica aguda; Nens; Trasplantament de cèl·lules mare


Introduction: Studies addressing the role of haploidentical as alternative to HLA-matched donors for stem cell transplantation (SCT) often include patients with diverse hematological malignancies in different remission statuses. Methods: We compared outcomes of children with acute lymphoblastic leukemia (ALL) undergoing SCT in second complete remission (CR2) from haploidentical (n = 25) versus HLA-matched donor (n = 51). Results: Patients were equally distributed across both groups according to age, immunophenotype, time to and site of relapse, relapse risk-group allocation, and minimal residual disease (MRD) before SCT. Incidence of graft failure, acute graft versus host disease (GVHD), and other early complications did not differ between both groups. We found no differences in overall survival (58.7% versus 59.5%; p = .8), leukemia free survival (LFS) (48% versus 36.4%; p = .5), event free survival (40% versus 34.4%; p = .69), cumulative incidence (CI) of subsequent relapse (28% versus 40.9%; p = .69), treatment related mortality (24% versus 23.6%; p = .83), CI of cGVHD (4.5% versus 18.7%; p = .2), and chronic GVHD-free and leukemia-free survival (44% versus 26.3%; p = .3) after haploidentical donor SCT. Chronic GVHD (HR = 0.09; p=.02) had protective impact, and MRD ≥ 0.01% before SCT (HR = 2.59; p=.01) had unfavorable impact on LFS. Discussion: These results support the role of haploidentical donor SCT in children with ALL in CR2.

Document Type

Article


Published version

Language

English

Publisher

Frontiers Media

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Frontiers in Pediatrics;11

https://doi.org/10.3389/fped.2023.1140637

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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