Better leukemia-free survival with allogeneic than with autologous HCT in AML patients with isolated trisomy 8: a study from the ALWP of the EBMT.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
02 2021
Historique:
received: 19 06 2020
accepted: 25 08 2020
revised: 04 08 2020
pubmed: 6 9 2020
medline: 22 6 2021
entrez: 5 9 2020
Statut: ppublish

Résumé

The indication for performing an allogeneic hematopoietic stem cell transplantation (allo-HCT) in patients with isolated trisomy 8 AML in first complete remission (CR) is still debated. Here, we compared outcomes of such patients given either allo-HCT or autologous (auto)-HCT. Inclusion criteria consisted of adult patients with de novo AML, isolated trisomy 8, first HCT between 2000 and 2018, CR1 at transplantation, and either auto-HCT or allo-HCT with a HLA-identical sibling donor (MSD) or a 10/10 HLA-matched unrelated donor (UD 10/10). A total of 401 patients met the inclusion criteria. They underwent an auto-HCT (n = 81), allo-HCT with a MSD (n = 186) or allo-HCT with a 10/10 UD (n = 134). At 3 years, relapse incidence, nonrelapse mortality and leukemia-free survival (LFS) were 59%, 5%, and 37%, respectively, in auto-HCT recipients; 31% (P < 0.001), 14% (P = 0.04), and 55% (P = 0.033), respectively, in MSD recipients and 29% (P < 0.001), 13% (P = 0.15), and 59% (P = 0.03), respectively, in UD 10/10 recipients. In multivariate analysis, in comparison to auto-HCT, MSD and UD 10/10 were associated with a lower risk of relapse (HR = 0.47, P < 0.001 and HR = 0.40, P < 0.001, respectively) translating to better LFS (HR = 0.69, P = 0.04 and HR = 0.60, P = 0.03, respectively). There was also a similar trend for overall survival (HR = 0.73, P = 0.12 and HR = 0.65, P = 0.08).

Identifiants

pubmed: 32887941
doi: 10.1038/s41409-020-01051-6
pii: 10.1038/s41409-020-01051-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

461-469

Subventions

Organisme : Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research)
ID : Senior research associate mandate

Références

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Auteurs

Frédéric Baron (F)

Laboratory of Hematology, GIGA-I3, University of Liege and CHU of Liège, Liege, Belgium. f.baron@ulg.ac.be.

Myriam Labopin (M)

EBMT Paris Study Office/CEREST-TC, Paris, France.
Department of Haematology, Saint Antoine Hospital, Paris, France.
INSERM UMR 938, Paris, France.
Sorbonne University, Paris, France.

Didier Blaise (D)

Department of Hematology, Institut Paoli Calmettes, Marseille, France.

Maija Itälä-Remes (M)

Stem Cell Transplantation Unit, HUCH Comprehensive Cancer Center, Helsinki, Finland.

Gérard Socié (G)

Hématologie-Greffe AP-HP Hôpital Saint Louis et Inserm U976, Université de Paris, Paris, France.

Edouard Forcade (E)

Service d'Hématologie Clinique et Thérapie Cellulaire, CHU Bordeaux, F-33000, Bordeaux, France.

Ibrahim Yakoub-Agha (I)

CHU de Lille, LIRIC, INSERM U995, Université de Lille, 59000, Lille, France.

Norbert Claude Gorin (NC)

Department of Haematology, Saint Antoine Hospital, Paris, France.

Jordi Esteve (J)

Hematology Department, Hospital Clínic de Barcelona, Barcelona, Spain.

Arnon Nagler (A)

EBMT Paris Study Office/CEREST-TC, Paris, France.
Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Ramat-Gan, Israel.

Mohamad Mohty (M)

EBMT Paris Study Office/CEREST-TC, Paris, France.
Department of Haematology, Saint Antoine Hospital, Paris, France.
INSERM UMR 938, Paris, France.
Sorbonne University, Paris, France.

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