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. 2017 Mar 29;9:97–102. doi: 10.2147/CMAR.S125259

Table 2.

Comparison of cytogenetic profile between AML patients with and without CNS involvement at diagnosis or relapse

Cytogenetic profile AML patients at diagnosis n=3,261
p-Value
Patients with CNS involvement at initial diagnosis and relapse n=55 Patients without CNS involvement at any time n=3,206
Normal karyotype, n (%) 16 (31) 1,472 (50) 0.158
Trisomy 8, n (%) 10 (21) 254 (8) 0.001
Trisomy 22, n (%) 3 (6) 62 (2) 0.034
Trisomy 11, n (%) 1 (2) 35 (1) 0.514
Trisomy 13, n (%) 1 (2) 42 (1) 0.641
Trisomy 21, n (%) 2 (4) 69 (2) 0.343
Monosomy 5, n (%) 0 (0) 26 (1) 0.531
Monosomy 7, n (%) 0 (0) 144 (4) 0.133
t(3;3), n (%) 0 (0) 8 (1) 0.729
t(1;7), n (%) 0 (0) 1 (0) 0.903
t(6;11), n (%) 1 (2) 6 (0) 0.005
t(8;21), n (%) 2 (4) 128 (4) 0.951
t(9;11), n (%) 3 (6) 41 (1) 0.003
t(6;9), n (%) 0 (0) 22 (1) 0.565
t(9;22), n (%) 0 (0) 7 (1) 0.746
t(11;19), n (%) 0 (0) 16 (1) 0.624
inv(16), n (%) 3 (6) 150 (5) 0.610
Inv(3) (q21q26) 0 (0) 20 (1) 0.583

Abbreviations: AML, acute myeloid leukemia; CNS, central nervous system.