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Items: 2

1.

Multilineage dysplasia does not influence prognosis in patients with CEBPA mutated AML supporting the WHO proposal to classify these patients as a unique entity

(Submitter supplied) By WHO 2008, CEBPA-mutated AML became a provisional subentity, but it remains to be clarified how CEBPAmut AML with multilineage dysplasia (MLD; ≥50% dysplastic cells in 2-3 lineages) but no other MDS-related feature should be classified. We investigated 108 CEBPAmut AML (15.7-87.6 years) for the impact of MLD and genetic features. MLD-positive patients differed from MLD-negative only by lower mean WBC counts (p=0.004), but not by other blood values, biologic characteristics, cytogenetic risk profiles, or additional molecular markers (NPM1mut, FLT3-ITD/TKD, RUNX1, MLL-PTD, IDH1/2). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4407
Platform:
GPL570
30 Samples
Download data: CEL
Series
Accession:
GSE33223
ID:
200033223
2.
Full record GDS4407

Biallelic CEBPA-mutated acute myeloid leukemia with multilineage dysplasia: peripheral blood mononuclear cells

Analysis of PBMCs from biallelic CEBPA (encoding CCAAT/enhancer binding protein)-mutated, acute myeloid leukemia (AML) patients with or without multilineage dysplasia (MLD). Cases without CEBPA mutations also examined. Results provide insight into the classification of CEBPA-mutated AML patients.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state, 2 genotype/variation sets
Platform:
GPL570
Series:
GSE33223
30 Samples
Download data: CEL
DataSet
Accession:
GDS4407
ID:
4407

Supplemental Content

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