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. 2020 Nov 20;40(11):1601–1606. [Article in Chinese] doi: 10.12122/j.issn.1673-4254.2020.11.10

1.

158例RUNX1基因突变及野生型AML患者的临床特征

Characteristics of 158 AML patients with and without RUNX1 mutations

Clinical characteristic Total (n=158) RUNX1mutated (n=19; 12.0%) RUNX1wildtype (n=139; 88.0%) P
Male/Female 158 11/8 78/61 0.883
Median age(year, range) 55.0 (45.0-65.0) 66.0 (51.0-75.0) 53.0 (43.0-63.5) 0.009
Median WBC count, ×109/L (range) 15.2 (2.7-68.4) 15.7 (3.2-89.7) 14.7 (2.1-67.7) 0.583
Median Hb, g/L (range) 76.0 (59.3-89.8) 72.0 (59.0-86.0) 76.0 (59.5-90.0) 0.726
Median Plt, ×109 (range) 34.5 (19.0-67.0) 40.0 (19.0-95.0) 34.0 (18.5-63.5) 0.247
Median BM blasts (range) 78.1 (50.5-90.1) 63.6 (39.5-84.1) 78.7 (55.7-90.2) 0.321
LDH 399.0 (230.0-785.0) 414.5 (264.8-1046.0) 399.0 (222-770) 0.452
FAB subtype (157 analysis)
  M1 13 2 11 1.000
  M2 62 4 58 0.079
  M3 15 0 15 0.274
  M4 29 6 23 0.209
  M5 37 7 30 0.244
  M6 1 0 1 1.000*
Surface antigen positivity
  CD34+ 72 10/9 62/77 0.510
  HLA-DR+ 76 12/7 64/75 0.161
  CD117+ 110 11/8 99/40 0.236
  CD13+ 64 9/10 55/84 0.516
  CD33+ 65 6/13 59/80 0.367
  CD38+ 68 10/9 58/81 0.368
  CD64+ 34 5/14 29/110 0.807
  CD36+ 20 5/14 15/124 0.123
  CD7+ 14 4/15 10/129 0.118