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

2.

RUNX1基因突变与预后核型及完全缓解的相关性

Correlation of RUNX1 mutations with prognostic karyotype and complete remission inAML patients

Variable Total RUNX1mutated RUNX1wildtype P
Age (year) 0.005
   ≥60 69 14 (20.28) 55 (79.71)
   < 60 89 5 (5.62) 84 (94.38)
CR rate (140 analysis) 71/140 (50.71) 3/19 (15.79) 68/121 (56.20) 0.001
Karyotype (152 analysis) 0.198
  Normal 75 12 (16.00) 63 (84.00)
  Abnormal 77 7 (9.09) 70 (90.91)
Cytogenetic risk group (152 analysis) 0.069
  Favorable 30 0 (0.00) 30 (22.56)
  Intermediate 72 11 (57.89) 61 (45.86)
  Adverse 50 8 (42.11) 42 (31.58)