Allogeneic stem cell transplantation in AML with t(6;9)(p23;q34);DEK-NUP214 shows a favourable outcome when performed in first complete remission.
Marina Díaz-BeyáMyriam LabopinJohan A MaertensMahmoud AljurfJakob PasswegDietrich Wilhelm BeelenHarry SchoutenGerard SociéNicolaas P M SchaapRainer SchwerdtfegerLiisa VolinMauricette MichalletEmmanuelle PolgeJorge SierraFlorent MalardAleksandra HolowieckaArnon Naglernull nullPublished in: British journal of haematology (2020)
Acute myeloid leukaemia (AML) with t(6;9)(p23;q34) is a poor-risk entity, commonly associated with FLT3-ITD (internal tandem duplication). Allogeneic stem-cell tranplantation (allo-SCT) is recommended, although studies analysing the outcome of allo-SCT in this setting are lacking. We selected 195 patients with t(6;9) AML, who received a first allo-SCT between 2000 and 2016 from the EBMT (European Society for Blood and Marrow Transplantation) registry. Disease status at time of allo-SCT was the strongest independent prognostic factor, with a two-year leukaemia-free survival and relapse incidence of 57% and 19% in patients in CR1 (first complete remission), 34% and 33% in CR2 (second complete remission), and 24% and 49% in patients not in remission, respectively (P < 0·001). This study, which represents the largest one available in t(6;9) AML, supports the recommendation to submit these patients to allo-SCT in CR1.
Keyphrases
- patient reported
- stem cell transplantation
- acute myeloid leukemia
- prognostic factors
- stem cells
- end stage renal disease
- bone marrow
- free survival
- allogeneic hematopoietic stem cell transplantation
- chronic kidney disease
- ejection fraction
- disease activity
- intensive care unit
- mesenchymal stem cells
- peritoneal dialysis
- tyrosine kinase
- systemic lupus erythematosus
- hepatitis b virus
- acute respiratory distress syndrome
- cell therapy