Haploidentical stem cell donor choice for patients with acute myeloid leukemia: A study from the ALWP of the EBMT.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
01 Mar 2024
Historique:
accepted: 30 01 2024
received: 07 11 2023
revised: 18 01 2024
medline: 2 3 2024
pubmed: 2 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

There is a paucity of information to guide selection of the most suitable stem cell donor in haploidentical (Haplo) hematopoietic stem cell transplantation (HSCT). For this reason, we conducted a retrospective analysis in order to evaluate the impact of Haplo family donors characteristics on HSCT outcomes in patients with acute myeloid leukemia (AML) who received graft-versus-host disease prophylaxis with post-transplant cyclophosphamide (PTCy). The primary endpoint was GvHD-free and relapse-free survival (GRFS). Overall, 2200 patients were included. The median age of donors was 37 years (range, 8-71), 820 (37%) were females, including 458 (21%) who were used for male recipients. Additionally, 1631 (74%) donated peripheral blood (PB). Multivariable analysis identified certain donor-related risk factors with a detrimental impact on transplant outcomes. The use of PB, older donor´s age and female donors to male recipients negatively affected GRFS. Donor´s age and female donor to male recipient combination also affected non-relapse mortality, leukemia-free survival and overall survival. In conclusion, donor-related variables significantly influence AML patient outcomes following Haplo-HSCT with PTCy. When possible, younger donors and male donors for male recipients should be prioritized. The use of BM can additionally prevent GVHD.

Identifiants

pubmed: 38429091
pii: 515172
doi: 10.1182/bloodadvances.2023012133
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Jaime Sanz (J)

Hospital Universitari i Politècnic La Fe, Valencia, Spain.

Myriam Labopin (M)

Hopital Saint Antoine, Paris, France.

Didier Blaise (D)

Institut Paoli Calmettes, Marseille, France.

Anna Maria Raiola (AM)

IRCCS Ospedale Policlinico San Martino, GENOVA, Italy.

Alessandro Busca (A)

A.O.U. Città della Salute e della Scienza, Turin, Italy.

Jan Vydra (J)

Institute of Hematology and Blood Transfusion, Prague, Czech Republic.

Johanna Tischer (J)

Ludwig-Maximilians-University of Munich, Klinikum Großhadern, Munich, Germany.

Patrice Chevallier (P)

CHU Hotel-Dieu, Nantes, France.

Stefania Bramanti (S)

IRCCS Istituto Clinico Humanitas, Rozzano, MI, Italy.

Renato Fanin (R)

Università degli Studi di Udine, Udine, Italy.

Gerard Socié (G)

Division of Hematology, Hospital Saint Louis & University Paris, Paris, France, Paris, France.

Edouard Forcade (E)

CHU Bordeaux, Pessac, France.

Nicolaus Kröger (N)

University Medical Center Hamburg_Eppendorf, Hamburg, Germany.

Yener Koc (Y)

Medicana International, ISTANBUL, Turkey.

Maija Itälä-Remes (M)

Turku University Hospital, Turku, Finland.

Marco Zecca (M)

Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Arnon Nagler (A)

Hematology and Bone Marrow Transplantation Division, Chaim Sheba Medical Center, Tel-Hashomer, Israel;, Tel Aviv, Israel.

Eolia Brissot (E)

Sorbonne Université, INSERM UMR-S 938, CRSA, service d'hématologie et thérapie cellulaire, AP-HP, Hôpital Saint-Antoine, Paris, France.

Alexandros Spyridonidis (A)

University Hospital of Patras, Rio, Patras, Greece.

Ali Bazarbachi (A)

American University of Beirut, Beirut, Lebanon.

Sebastian Giebel (S)

Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.

Simona Piemontese (S)

San Raffaele Scientific Institute, MILANO, Italy.

Mohamad Mohty (M)

Hôpital Saint-Antoine, INSERM UMRs 938, and Université Sorbonne, Paris, France.

Fabio Ciceri (F)

San Raffaele Scientific Institute, Milano, Italy.

Classifications MeSH