Literature DB >> 32020596

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-Beyá1,2, Myriam Labopin3, Johan Maertens4, Mahmoud Aljurf5, Jakob Passweg6, Beelen Dietrich7, Harry Schouten8, Gerard Socié9, Nicolaas Schaap10, Rainer Schwerdtfeger11, Liisa Volin12, Mauricette Michallet13, Emmanuelle Polge3, Jorge Sierra14, Mohamad Mohty3,15, Jordi Esteve1,2,16, Arnon Nagler3,17.   

Abstract

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.
© 2020 British Society for Haematology and John Wiley & Sons Ltd.

Entities:  

Keywords:  AML; DEK-NUP214; allo-SCT; prognosis; t(6;9) AML

Mesh:

Substances:

Year:  2020        PMID: 32020596     DOI: 10.1111/bjh.16433

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  2 in total

Review 1.  Relapsed acute myeloid leukemia in children and adolescents: current treatment options and future strategies.

Authors:  Sara Zarnegar-Lumley; Kenneth J Caldwell; Jeffrey E Rubnitz
Journal:  Leukemia       Date:  2022-06-06       Impact factor: 12.883

2.  Gilteritinib monotherapy as a transplant bridging option for high risk FLT3-mutated AML with t(6;9)(p23;q34.1);DEK-NUP214 in morphological but not cytogenetic or molecular remission following standard induction chemotherapy.

Authors:  James W Day; Thomas A Fox; Rajeev Gupta; Asim Khwaja; Andrew J Wilson; Panagiotis D Kottaridis
Journal:  Leuk Res Rep       Date:  2022-02-07
  2 in total

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