TY - JOUR
T1 - Comparing outcomes of a second allogeneic hematopoietic cell transplant using HLA-matched unrelated versus T-cell replete haploidentical donors in relapsed acute lymphoblastic leukemia
T2 - a study of the Acute Leukemia Working Party of EBMT
AU - Kharfan-Dabaja, Mohamed A
AU - Labopin, Myriam
AU - Bazarbachi, Ali
AU - Ciceri, Fabio
AU - Finke, Jürgen
AU - Bruno, Benedetto
AU - Bornhäuser, Martin
AU - Gedde-Dahl, Tobias
AU - Labussière-Wallet, Hélène
AU - Niittyvuopio, Riitta
AU - Valerius, Thomas
AU - Angelucci, Emanuele
AU - Brecht, Arne
AU - Caballero, Dolores
AU - Kuball, Jürgen
AU - Potter, Victoria
AU - Schmid, Christoph
AU - Tischer, Johanna
AU - Zuckerman, Tsila
AU - Benedetti, Fabio
AU - Blaise, Didier
AU - Diez-Martin, Jose Luis
AU - Sanz, Jaime
AU - Ruggeri, Annalisa
AU - Brissot, Eolia
AU - Savani, Bipin N
AU - Giebel, Sebastian
AU - Nagler, Arnon
AU - Mohty, Mohamad
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/9
Y1 - 2021/9
N2 - Optimal donor choice for a second allogeneic hematopoietic cell transplant (allo-HCT) in relapsed acute lymphoblastic leukemia (ALL) remains undefined. We compared outcomes using HLA-matched unrelated donors (MUD) versus haploidentical donors in this population. Primary endpoint was overall survival (OS). The MUD allo-HCT group comprised 104 patients (male = 56, 54%), median age 36 years, mostly (76%) with B-cell phenotype in complete remission (CR) (CR2/CR3 + = 76, 73%). The 61 patients (male = 38, 62%) in the haploidentical group were younger, median age 30 years (p = 0.002), had mostly (79%) a B-cell phenotype and the majority were also in CR at time of the second allo-HCT (CR2/CR3 + = 40, 66%). Peripheral blood stem cells was the most common cell source in both, but a significantly higher number in the haploidentical group received bone marrow cells (26% vs. 4%, p < 0.0001). A haploidentical donor second allo-HCT had a 1.5-fold higher 2-year OS (49% vs. 31%), albeit not statistically significant (p = 0.13). A longer time from first allo-HCT to relapse was associated with improved OS, leukemia-free survival, graft-versus-host disease-free-relapse-free survival, and lower cumulative incidences of relapse and non-relapse mortality. Results suggest no major OS difference when choosing either a MUD or haploidentical donor for ALL patients needing a second allo-HCT.
AB - Optimal donor choice for a second allogeneic hematopoietic cell transplant (allo-HCT) in relapsed acute lymphoblastic leukemia (ALL) remains undefined. We compared outcomes using HLA-matched unrelated donors (MUD) versus haploidentical donors in this population. Primary endpoint was overall survival (OS). The MUD allo-HCT group comprised 104 patients (male = 56, 54%), median age 36 years, mostly (76%) with B-cell phenotype in complete remission (CR) (CR2/CR3 + = 76, 73%). The 61 patients (male = 38, 62%) in the haploidentical group were younger, median age 30 years (p = 0.002), had mostly (79%) a B-cell phenotype and the majority were also in CR at time of the second allo-HCT (CR2/CR3 + = 40, 66%). Peripheral blood stem cells was the most common cell source in both, but a significantly higher number in the haploidentical group received bone marrow cells (26% vs. 4%, p < 0.0001). A haploidentical donor second allo-HCT had a 1.5-fold higher 2-year OS (49% vs. 31%), albeit not statistically significant (p = 0.13). A longer time from first allo-HCT to relapse was associated with improved OS, leukemia-free survival, graft-versus-host disease-free-relapse-free survival, and lower cumulative incidences of relapse and non-relapse mortality. Results suggest no major OS difference when choosing either a MUD or haploidentical donor for ALL patients needing a second allo-HCT.
UR - http://www.scopus.com/inward/record.url?scp=85105151564&partnerID=8YFLogxK
U2 - 10.1038/s41409-021-01317-7
DO - 10.1038/s41409-021-01317-7
M3 - Article
C2 - 33931757
SN - 0268-3369
VL - 56
SP - 2194
EP - 2202
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 9
ER -