Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT

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Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT. / Kharfan-Dabaja, Mohamed A; Labopin, Myriam; Ayala, Ernesto; Bazarbachi, Ali; Blaise, Didier; Vydra, Jan; Bramanti, Stefania; Itälä-Remes, Maija; Schmid, Christoph; Busca, Alessandro; Forcade, Edouard; Rabitsch, Werner; Zecca, Marco; Kröger, Nicolaus; Bulabois, Claude-Eric; Grillo, Giovanni; Rambaldi, Alessandro; Fanin, Renato; Zallio, Francesco; Di Renzo, Nicola; Koc, Yener; Novis, Yana; McDonald, Andrew; Herrera Arroyo, Concepcion; Sanz, Jaime; Nagler, Arnon; Ciceri, Fabio; Mohty, Mohamad.

In: HEMASPHERE, Vol. 7, No. 7, 07.2023, p. e920.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Kharfan-Dabaja, MA, Labopin, M, Ayala, E, Bazarbachi, A, Blaise, D, Vydra, J, Bramanti, S, Itälä-Remes, M, Schmid, C, Busca, A, Forcade, E, Rabitsch, W, Zecca, M, Kröger, N, Bulabois, C-E, Grillo, G, Rambaldi, A, Fanin, R, Zallio, F, Di Renzo, N, Koc, Y, Novis, Y, McDonald, A, Herrera Arroyo, C, Sanz, J, Nagler, A, Ciceri, F & Mohty, M 2023, 'Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT', HEMASPHERE, vol. 7, no. 7, pp. e920. https://doi.org/10.1097/HS9.0000000000000920

APA

Kharfan-Dabaja, M. A., Labopin, M., Ayala, E., Bazarbachi, A., Blaise, D., Vydra, J., Bramanti, S., Itälä-Remes, M., Schmid, C., Busca, A., Forcade, E., Rabitsch, W., Zecca, M., Kröger, N., Bulabois, C-E., Grillo, G., Rambaldi, A., Fanin, R., Zallio, F., ... Mohty, M. (2023). Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT. HEMASPHERE, 7(7), e920. https://doi.org/10.1097/HS9.0000000000000920

Vancouver

Bibtex

@article{fb4621441cb3430b9cface991df9d8d2,
title = "Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT",
abstract = "Availability of haploidentical donors has broadened utilization of allogeneic hematopoietic cell transplantation (allo-HCT). Peripheral blood stem cells (PBSC) are being used with increased frequency in haploidentical allo-HCT. We evaluated extent of HLA disparity (2-3/8 versus 4/8 HLA antigen mismatches) on post-allograft outcomes when using T-cell replete PBSC from haploidentical donors for acute myeloid leukemia in first complete remission. Primary objectives entailed assessing cumulative incidence of grade 2-4 acute graft-versus-host disease (GVHD) and chronic GVHD (any grade). A total of 645 patients received a haploidentical allo-HCT from a donor with either 2-3 of 8 HLA antigen mismatches (n = 180) or with 4 of 8 HLA antigen mismatches (n = 465). Presence of 2-3 of 8 versus 4 of 8 HLA mismatches did not affect the incidence of acute GVHD (grade 2-4) and chronic GVHD (any grade). Overall survival (OS), leukemia-free survival (LFS) relapse incidence (RI), nonrelapse mortality and the composite endpoint of GVHD-free relapse-free survival were also similar among the groups. Pertaining to HLA-B leader matching effect, our analysis did not discern any difference in aforementioned post-allograft outcomes for this variable. However, in univariate analysis, absence of an antigen mismatch in HLA-DPB1 showed a trend for better OS. Notwithstanding inherent limitations associated with registry data, our results did not show an advantage of selecting a haploidentical donor with 2-3 of 8 HLA antigen mismatches over one with 4 of 8 HLA antigen mismatches when using PBSC as the cell source. Adverse cytogenetics remains a major adverse determinant of inferior OS and LFS and a higher RI. Using reduced-intensity conditioning yielded worse OS and LFS.",
author = "Kharfan-Dabaja, {Mohamed A} and Myriam Labopin and Ernesto Ayala and Ali Bazarbachi and Didier Blaise and Jan Vydra and Stefania Bramanti and Maija It{\"a}l{\"a}-Remes and Christoph Schmid and Alessandro Busca and Edouard Forcade and Werner Rabitsch and Marco Zecca and Nicolaus Kr{\"o}ger and Claude-Eric Bulabois and Giovanni Grillo and Alessandro Rambaldi and Renato Fanin and Francesco Zallio and {Di Renzo}, Nicola and Yener Koc and Yana Novis and Andrew McDonald and {Herrera Arroyo}, Concepcion and Jaime Sanz and Arnon Nagler and Fabio Ciceri and Mohamad Mohty",
note = "Copyright {\textcopyright} 2023 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association.",
year = "2023",
month = jul,
doi = "10.1097/HS9.0000000000000920",
language = "English",
volume = "7",
pages = "e920",
journal = "HEMASPHERE",
issn = "2572-9241",
publisher = "Wolters Kluwer Health",
number = "7",

}

RIS

TY - JOUR

T1 - Significance of Degree of HLA Disparity Using T-cell Replete Peripheral Blood Stem Cells From Haploidentical Donors With Posttransplantation Cyclophosphamide in AML in First Complete Hematologic Remission: A Study of the Acute Leukemia Working Party of the EBMT

AU - Kharfan-Dabaja, Mohamed A

AU - Labopin, Myriam

AU - Ayala, Ernesto

AU - Bazarbachi, Ali

AU - Blaise, Didier

AU - Vydra, Jan

AU - Bramanti, Stefania

AU - Itälä-Remes, Maija

AU - Schmid, Christoph

AU - Busca, Alessandro

AU - Forcade, Edouard

AU - Rabitsch, Werner

AU - Zecca, Marco

AU - Kröger, Nicolaus

AU - Bulabois, Claude-Eric

AU - Grillo, Giovanni

AU - Rambaldi, Alessandro

AU - Fanin, Renato

AU - Zallio, Francesco

AU - Di Renzo, Nicola

AU - Koc, Yener

AU - Novis, Yana

AU - McDonald, Andrew

AU - Herrera Arroyo, Concepcion

AU - Sanz, Jaime

AU - Nagler, Arnon

AU - Ciceri, Fabio

AU - Mohty, Mohamad

N1 - Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association.

PY - 2023/7

Y1 - 2023/7

N2 - Availability of haploidentical donors has broadened utilization of allogeneic hematopoietic cell transplantation (allo-HCT). Peripheral blood stem cells (PBSC) are being used with increased frequency in haploidentical allo-HCT. We evaluated extent of HLA disparity (2-3/8 versus 4/8 HLA antigen mismatches) on post-allograft outcomes when using T-cell replete PBSC from haploidentical donors for acute myeloid leukemia in first complete remission. Primary objectives entailed assessing cumulative incidence of grade 2-4 acute graft-versus-host disease (GVHD) and chronic GVHD (any grade). A total of 645 patients received a haploidentical allo-HCT from a donor with either 2-3 of 8 HLA antigen mismatches (n = 180) or with 4 of 8 HLA antigen mismatches (n = 465). Presence of 2-3 of 8 versus 4 of 8 HLA mismatches did not affect the incidence of acute GVHD (grade 2-4) and chronic GVHD (any grade). Overall survival (OS), leukemia-free survival (LFS) relapse incidence (RI), nonrelapse mortality and the composite endpoint of GVHD-free relapse-free survival were also similar among the groups. Pertaining to HLA-B leader matching effect, our analysis did not discern any difference in aforementioned post-allograft outcomes for this variable. However, in univariate analysis, absence of an antigen mismatch in HLA-DPB1 showed a trend for better OS. Notwithstanding inherent limitations associated with registry data, our results did not show an advantage of selecting a haploidentical donor with 2-3 of 8 HLA antigen mismatches over one with 4 of 8 HLA antigen mismatches when using PBSC as the cell source. Adverse cytogenetics remains a major adverse determinant of inferior OS and LFS and a higher RI. Using reduced-intensity conditioning yielded worse OS and LFS.

AB - Availability of haploidentical donors has broadened utilization of allogeneic hematopoietic cell transplantation (allo-HCT). Peripheral blood stem cells (PBSC) are being used with increased frequency in haploidentical allo-HCT. We evaluated extent of HLA disparity (2-3/8 versus 4/8 HLA antigen mismatches) on post-allograft outcomes when using T-cell replete PBSC from haploidentical donors for acute myeloid leukemia in first complete remission. Primary objectives entailed assessing cumulative incidence of grade 2-4 acute graft-versus-host disease (GVHD) and chronic GVHD (any grade). A total of 645 patients received a haploidentical allo-HCT from a donor with either 2-3 of 8 HLA antigen mismatches (n = 180) or with 4 of 8 HLA antigen mismatches (n = 465). Presence of 2-3 of 8 versus 4 of 8 HLA mismatches did not affect the incidence of acute GVHD (grade 2-4) and chronic GVHD (any grade). Overall survival (OS), leukemia-free survival (LFS) relapse incidence (RI), nonrelapse mortality and the composite endpoint of GVHD-free relapse-free survival were also similar among the groups. Pertaining to HLA-B leader matching effect, our analysis did not discern any difference in aforementioned post-allograft outcomes for this variable. However, in univariate analysis, absence of an antigen mismatch in HLA-DPB1 showed a trend for better OS. Notwithstanding inherent limitations associated with registry data, our results did not show an advantage of selecting a haploidentical donor with 2-3 of 8 HLA antigen mismatches over one with 4 of 8 HLA antigen mismatches when using PBSC as the cell source. Adverse cytogenetics remains a major adverse determinant of inferior OS and LFS and a higher RI. Using reduced-intensity conditioning yielded worse OS and LFS.

U2 - 10.1097/HS9.0000000000000920

DO - 10.1097/HS9.0000000000000920

M3 - SCORING: Journal article

C2 - 37388926

VL - 7

SP - e920

JO - HEMASPHERE

JF - HEMASPHERE

SN - 2572-9241

IS - 7

ER -