Skip to main content

Table 3 Clinical and laboratory data among homozygous carriers of P2 allele versus heterozygous group and non-carriers

From: Interleukin-4 gene intron 3 VNTR polymorphism in adult acute myeloid leukemia

Variables

P1P1 and P1P2 (n = 26)

P2P2 (n = 34)

P value

Age (years), Mean ± SD

37.1 ± 11.50

47.6 ± 14.70

0.004

Sex, n (%)

0.909

 Male

18 (69.2)

24 (70.6)

 Female

8 (30.8)

10 (29.4)

Extramedullary involvement, n (%)

0.700

 Positive

12 (46.2)

14 (41.2)

 Negative

14 (53.8)

20 (58.8)

TLC (× 103/µL), Median (IQR)

12.6 (4.5–30)

28 (15–130)

0.025

Hemoglobin (g/dL),

0.120

 Mean ± SD

7.82 ± 2.21

7.2 ± 2.1

Platelets (× 103/µL), × 109/L), Median (IQR)

66 (18 -141)

19 (13–62)

0.010

PB blasts (%)

0.005

Median (IQR)

20 (2–49)

58 (33–69)

BM blasts (%),Median (IQR)

60 (38–80)

80 (67–85)

0.023

FAB Subtype, n (%)

0.973

 M0, M1

6 (23.1%)

8 (23.5%)

 M2

14 (53.8%)

19 (55.9%)

 M4/5, M6, M7

6 (23.1%)

7 (20.6%)

Immunophenotyping, n (%)

 HLA-DR

22 (84.6)

31 (91.2)

0.432

 CD34

21 (80.8)

28 (82.4)

0.874

 MPOX

20 (76.9)

30 (88.2)

0.244

Cytogenetic risk groups, n (%)*

0.32

 Favorable

4 (19)

3 (10)

 Intermediate and poor

16 (61.53)

27 (90)

Complete remission

23 (88.55)

22 (64.7%)

0.035

  1. Bold values indicate significant p value
  2. *Six patients (23%) from (P1P2 + P1P1) group and four patients (11.76%) from P2P2 group were excluded due to non -provided data or failed cytogenetic analysis
  3. MPOX myeloperoxidase; Favorable cytogenetic markers: t(8;21), inv(16); Intermediate cytogenetic markers: normal karyotype, trisomy 8; Unfavorable cytogenetic markers t(11q23), t(9;11), monosomy7