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. 2017 Sep 18;14(5):6269–6276. doi: 10.3892/ol.2017.6988

Table VIII.

Clinical characteristics between patients with AML-M3 carrying the T allele, and those carrying the C allele.

Patients with AML-M3 (T152C variation)

Characteristic Total (n=78) T (n=46) C (n=32) P-value
Sex (female/male) 31/47 23/23 8/24 0.026a
Age (years, mean ± SD) 39.21±13.11 41.04±14.21 36.56±11.03 0.139
Peripheral blood [median(P25-P75)]
  Hb (g/l) 73.50 (63.75–103.00) 73.50 (65.25–100.50) 74.00 (57.75–110.50) 0.851
  WBC (×109 cells/l) 3.66 (1.44–11.25) 2.81 (1.27–8.39) 5.16 (2.04–17.24) 0.065
  PLT (×109 cells/l) 15.00 (10.00–29.00) 13.50 (10.00–27.00) 18.50 (10.75–31.25) 0.427
  Hypocytosis, n (%) 31 (39.7) 19 (41.3) 12 (37.5) 0.785
  HLAL, n (%) 5 (6.4) 2 (4.3) 3 (9.4) 0.390
  PML-RARα, n (%) 72 (92.3) 41 (89.1) 31 (96.9) 0.392
Chemotherapy responseb
  Remission at third month, n (%) 53 (93.0) 31 (91.2) 22 (95.7) 1.000
  Remission duration [days, median (P25-P75)] 42.00 (34.00–60.00) 44.00 (35.00–61.75) 41.00 (34.00–57.00) 0.782
a

OR, 3.000, 95% CI, 1.118–8.050

b

Completeclinical data were collected from 57 cases, 23 cases of which carried T152C variation. HLAL, hyperleukocytic acute leukemia; AML, acute myeloid leukemia; PML, promyelocytic leukemia; RARα, retinoic acid α receptor; WBC, white blood cell; PLT, platelet; Hb, hemoglobin; SD, standard deviation; OR, odds ratio; CI, confidence interval.