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Table 1 Patient characteristics

From: Integrative study of EZH2 mutational status, copy number, protein expression and H3K27 trimethylation in AML/MDS patients

 

AML

Myeloid Neoplasms (Non-AML)

Total

51

7

Subtype (%)

AML with recurrent

MDS-MLD: 2

 

genetic abnormalities: 20 (39)

MDS-EB-2: 1

 

AML-MRC: 22 (43)

CMML-2: 1

 

t-AML: 4 (8)

MDS/MPN: 2

 

AML, NOS: 5 (10)

CNL: 1

Age (years; median and range)

63 (20–86)

69 (42–84)

Sex

  

 Male

25

4

 Female

26

3

EZH2-mutated patients (%)

6 (12)

7 (100)

Mutations per patient (median and range)

3 (0–7)

4 (3–7)

Del(7q) or -7 (%)

13 (25)

2 (29)

WBC (× 109/L; median and range)

10.4 (0.6–192.6)

18.4 (1.6–126.5)

BM blasts (%; median and range)

63 (10–100)

4 (1–16)

Treatment

  

 Induction chemotherapy (%)

31 (61)

0

 HSCT (%)

27 (53)

4 (57)

 Non-intensive therapy (%)

13 (25)

3 (43)

  1. AML-MRC acute myeloid leukemia with myelodysplasia-related changes, BM bone marrow, CMML chronic myelomonocytic leukemia, CNL chronic neutrophilic leukemia, HSCT hematopoietic stem cell transplantation, MDS-EB myelodysplastic syndrome with excess blasts, MDS-MLD MDS with multilineage dysplasia, MPN myeloproliferative neoplasm, NOS not otherwise specified, WBC white blood cells, t-AML therapy-related AML