Allogeneic hematopoietic cell transplantation for acute myeloid leukemia with hyperdiploid complex karyotype.


Journal

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

Informations de publication

Date de publication:
13 Dec 2023
Historique:
received: 11 06 2023
accepted: 29 11 2023
revised: 23 10 2023
medline: 14 12 2023
pubmed: 14 12 2023
entrez: 13 12 2023
Statut: aheadofprint

Résumé

Allogeneic hematopoietic cell transplantation (allo-HCT) remains the best consolidation strategy for acute myeloid leukemia (AML) with complex karyotype (CK). However, CK is a heterogenous and highly diverse entity. Numerical abnormalities have been associated with a controversial prognosis and AML with only multiple numerical abnormalities known as pure hyperdiploid karyotype (HDK) may have a distinct prognosis after allo-HCT compared to non-pure HDK CK AML. A total of 236 patients were identified within the EBMT registry as having HDK comprising 95 pure (pHDK) and 141 with other cytogenetic abnormalities (HDK+). The 2-year probability of leukemia-free survival (LFS) was 50% for pHDK and 31% for HDK+ (p = 0.003). The 2-year probability of overall survival (OS) was 57% for pHDK and 36% for HDK+ (p = 0.007). The 2-year cumulative incidence of relapse (RI) was 22% for pHDK and 44% for HDK+ (p = 0.001). The 2-year probability of graft-versus-host disease (GvHD)-free and relapse-free survival (GRFS) was 36% for pHDK and 21% for HDK+ (p = 0.01). On multivariate analysis, pHDK remained associated with significantly better LFS, OS and GRFS and lower RI (all p-values <0.004). pHDK AML constitutes probably a distinct cytogenetic entity from HDK+ or other non-hyperdiploid CK AML with better outcomes after allo-HCT.

Identifiants

pubmed: 38092959
doi: 10.1038/s41409-023-02167-1
pii: 10.1038/s41409-023-02167-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Xavier Poiré (X)

Section of Hematology, Institut Roi Albert II, Cliniques Universitaires St-Luc, Brussels, Belgium. Xavier.Poire@saintluc.uclouvain.be.

Myriam Labopin (M)

Acute Leukemia Working Party of the EBMT, Paris, France.
Université Pierre et Marie Curie, Paris, France.
INSERM UMR 938, Paris, France.
Service d'Hématologie, Hôpital Saint-Antoine, Paris, France.

Emmanuelle Polge (E)

Acute Leukemia Working Party of the EBMT, Paris, France.
Université Pierre et Marie Curie, Paris, France.
INSERM UMR 938, Paris, France.
Service d'Hématologie, Hôpital Saint-Antoine, Paris, France.

Arnold Ganser (A)

Hannover Medical School, Hannover, Germany.

Gérard Socié (G)

Department of Hematology, Bone Marrow Transplantation, Hôpital Saint-Louis, Paris, France.

Tobias Gedde-Dahl (T)

Oslo University Hospital, Rikshospitalet, Oslo, Norway.

Edouard Forcade (E)

CHU Bordeaux, Hôpital Haut-Leveque, Pessac, France.

Jürgen Finke (J)

Universitätsklinikum Freidburg, Department of Medicine, Hematology, Oncology, Freidburg, Germany.

Yves Chalandon (Y)

Hôpitaux Universitaires de Genève, Département d'Oncologie, Service d'Hématologie, Genève, Switzerland.

Claude-Eric Bulabois (CE)

CHU Grenoble-Alpes, Université Grenoble-Alpes, Grenoble, France.

Ibrahim Yakoub-Agha (I)

CHU de Lille, Université de Lille, INSERM U1286, Infinite, 5900, Lille, France.

Mahmoud Aljurf (M)

King Faisal Specialist Hospital & Research Center, Section of Adult Haematology/BMT, Riyadh, Saudi Arabia.

Nicolaus Kröger (N)

University Hospital Eppendorf, Bone Marrow Transplantation Centre, Hamburg, Germany.

Igor Wolfgang Blau (IW)

Medizinische Klinik m. S. Hämatologie, Onkologie und Tumorimmunologie, Charité Universitätsmedizin, Berlin, Germany.

Arnon Nagler (A)

Chaim Sheba Medical Center, Tel-Hashomer, Israel.

Jordi Esteve (J)

Hematology department, Hospital Clinic, Barcelona, Spain.

Mohamad Mohty (M)

Acute Leukemia Working Party of the EBMT, Paris, France.
Université Pierre et Marie Curie, Paris, France.
INSERM UMR 938, Paris, France.
Service d'Hématologie, Hôpital Saint-Antoine, Paris, France.

Classifications MeSH