Cord blood transplantation for AML: Comparable LFS in patients with de novo versus secondary AML in CR1, an ALWP/EBMT study.
Fréderic BaronArnon NaglerJacques-Emmanuel GalimardJaime SanzJurjen VersluisEdouard ForcadePatrice ChevallierAnne SirventChloe AnthiasJürgen KuballSabine FurstAlessandro RambaldiJorge SierraPeter A von dem BorneMaria Pilar Gallego HernanzThomas CluzeauStephen RobinsonAnna Maria RaiolaHélène Labussière-WalletJenny L ByrneJean-Valère MalfusonAnnalisa RuggeriMohamad MohtyFabio CiceriPublished in: British journal of haematology (2023)
We investigated whether secondary versus de novo acute myeloid leukaemia (AML) would be associated with poor outcomes in adult acute AML patients in first complete remission (CR1) receiving unrelated cord blood transplantation (CBT). This is a retrospective study from the acute leukaemia working party of the European Society for Blood and Marrow Transplantation. Inclusion criteria included adult at first allogeneic haematopoietic cell transplantation between 2000 and 2021, unrelated single or double unit CBT, AML in CR1, no ex vivo T-cell depletion and no post-transplant cyclophosphamide. The primary end-point of the study was leukaemia-free survival (LFS). A total of 879 patients with de novo (n = 696) or secondary (n = 183) AML met the inclusion criteria. In multivariable analyses, sAML patients had non-significantly different LFS (HR = 0.98, p = 0.86), overall survival (HR = 1.07, p = 0.58), relapse incidence (HR = 0.74, p = 0.09) and non-relapse mortality (HR = 1.26, p = 0.13) than those with de novo AML. Our results demonstrate non-significantly different LFS following CBT in adult patients with secondary versus de novo AML.
Keyphrases
- acute myeloid leukemia
- cord blood
- free survival
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- liver failure
- newly diagnosed
- ejection fraction
- chronic kidney disease
- cell therapy
- respiratory failure
- bone marrow
- drug induced
- stem cells
- cardiovascular disease
- aortic dissection
- low dose
- patient reported outcomes
- single cell
- coronary artery disease
- young adults
- mesenchymal stem cells
- high dose
- systemic lupus erythematosus
- mass spectrometry
- cardiovascular events
- atomic force microscopy
- hematopoietic stem cell