Multilineage dysplasia as assessed by immunophenotype has no impact on clinical-biological features and outcome of NPM1-mutated acute myeloid leukemia.

Abstract:

:The presence of multilineage dysplasia (MLD) by morphology at diagnosis in acute myeloid leukemia (AML) defines a separate subset in the World Health Organization classification with still-debated prognostic value. A major controversy concerns MLD's role in NPM1-mutated (NPM1⁺) AML, which correlates with good prognosis. We used flow cytometry (FC), an emerging technique for assessing dysplasia, to investigate MLD in NPM1⁺ AML by an immunophenotypic score (IPS), a technique previously adopted in myelodysplastic syndrome. Eighty-five intensively treated NPM1⁺ AML cases were studied. Patients were grouped according to the combination of data in maturing cell compartments. FC-assessed dysplasia showed a significant correlation with morphology-assessed dysplasia, showing the efficacy of this method in highlighting dysplasia in AML. Except for MLD, IPS did not influence any patient- or disease-related characteristics at diagnosis. Furthermore, IPS did not influence complete remission rate, disease-free survival, or overall survival. By investigating NPM1 status on separated cell compartments, we established a correlation between FC-assessed MLD and belonging to AML clone. This study shows that dysplasia evaluated by immunophenotype has no impact on clinical-biological characteristics or on outcome of NPM1⁺ AML. Dysplasia is part of the spectrum of NPM1⁺ AML, and the prognostic stratification of this category of patients should not be based upon it.

journal_name

Exp Hematol

journal_title

Experimental hematology

authors

Mannelli F,Ponziani V,Bonetti MI,Bencini S,Cutini I,Gianfaldoni G,Scappini B,Pancani F,Rondelli T,Benelli M,Caporale R,Grazia Gelli AM,Peruzzi B,Longo G,Bosi A

doi

10.1016/j.exphem.2015.06.003

subject

Has Abstract

pub_date

2015-10-01 00:00:00

pages

869-879.e22

issue

10

eissn

0301-472X

issn

1873-2399

pii

S0301-472X(15)00208-8

journal_volume

43

pub_type

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