Skip to main content

Table 1 Demographic, clinical, and laboratory characteristics of the studied AML patients

From: Reductive regulation of BECN1 gene in adult Egyptian patients with do novo AML

Parameter

AML patients (total no. = 50)

Sex [n (%)]

 Females

28 (56.0%)

 Males

22 (44.0%)

Age (years)

 Mean ± SD

(51.56 ± 20.17)

Clinical data [n (%)]

 Fever

11(22.0%)

 Hepatomegaly

19(38.0%)

 Splenomegaly

19(38.0%)

 Lymphadenopathy

4(8.0%)

TLC (x109/L) (Median—IQR)

54.8 (22.3–76.4)

Hb (g/dl) (Mean ± SD)

(8.09 ± 2.01)

PLT (x109/L) (Median—IQR)

33 (24–68)

PB blasts (%) (Mean ± SD)

(56.96 ± 23.43)

BM blasts (%) (Mean ± SD)

(75.68 ± 20.83)

Immunophenotyping [n (%)]

 CD34 +

33 (66.0%)

 CD117 +

32 (64.0%)

 HLA-DR +

43 (86.0%)

FAB subtypes [n (%)]

 M0

5 (10.0%)

 M1

10 (20.0%)

 M2

20 (40.0%)

 M3

5 (10.0%)

 M4

7 (14.0%)

 M5

3(6.0%)

Molecular abnormalities [n (%)]

 Wild type NPM1

5 (10.0%)

 Mutated NPM1 and FLT3-ITD

2 (4.0%)

 FLT3-ITD mutation

14 (28.0%)

 c-KIT mutation

8 (16.0%)

Cytogenetic risk groups [n (%)]

 Favourable

11 (22.0%)

 Intermediate

10 (20.0%)

 Adverse

29 (58.0%)

Response to induction therapy (D28) [n (%)]

 Responders

15 (30.0%)

 Non- responders

35 (70.0%)

  1. TLC total leukocytic count, Hb haemoglobin, PLT platelets, BM bone marrow, PB peripheral blood, FAB French American British, SD standard deviation, IQR interquartile range, NPM1 Nucleophosmin, ITD internal tandem duplication