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. 2010 Apr 13;89(9):861–871. doi: 10.1007/s00277-010-0948-7

Table 1.

Summary of patient’s clinical parameters

Patient ID FAB % CD34+ BM/PB Expansion Karyotype FLT3-ITD KIT mutation
1 M7 43 PB Yes −7; +21
2 M2 26 PB Yes BCR-ABL, inv (16) ND
3 M2 42 BM Yes t(8;21) +
4 M2 52 PB Yes N + ND
5 M0 22 PB Yes N +
6 M5 88 PB Yes N ND
7 M1 70 BM Yes +3q;−7;−10
8 M0 70 BM Yes 5q−;+6 ND
9 M1 19 PB Yes N +
10 M1 19 PB Yes N ND ND
11 M1 35 BM Yes N +
12 M5 14 PB Yes t(11;20) +
13 M1 57 PB Yes N
14 M5 10 BM Yes ND ND
15 M5 0.5 PB Yes N + ND
16 M1 63 PB No 3p+; −7; +8
17 M1 29 PB No del (9) +
18 M4 17 PB No inv (16) +
19 M5 13 BM No N + ND

AML cells derived from bone marrow (BM) or peripheral blood (PB); Percentage of CD34+ (% CD34+) in the total AML mononuclear cell fraction; AML CD34+ cells cultured in long-term culture assay demonstrated an expansion (y/n); FAB, French-American-British classifications; FLT3-ITD (internal tandem duplication) was present (+) or absent (−) in the AML cells; ND, not determined; N, normal