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. Author manuscript; available in PMC: 2020 Feb 1.
Published in final edited form as: Mol Cancer Ther. 2019 Jun 4;18(8):1451–1459. doi: 10.1158/1535-7163.MCT-18-1125

Table 1.

Comparison of clinical and molecular characteristics by low and high long non-coding RNA (lncRNA) score in the cohort of 76 older patients (aged ≥60 years) with cytogenetically normal acute myeloid leukemia, who were analyzed with the nCounter assay.

Characteristic Low lncRNA Score (n=38) High lncRNA Score (n=38) P
Age, years 0.04
 Median 66 71
 Range 60–81 60–82

Sex, n (%) of females 21 (55) 19 (50) 0.82

Race, n (%) 1.00
 White 35 (95) 34 (92)
 Non-white 2 (5) 3 (8)

Hemoglobin, g/dL 0.15
 Median 9 9.4
 Range 6.5–11.9 6.8–11.3

Platelet count, x109/L 0.67
 Median 70 70
 Range 18–507 5–592

WBC count, x109/L 0.54
 Median 29.7 28.5
 Range 1.4–343.6 1.0–173.1

Blood blasts, % 0.18
 Median 36 58
 Range 0–90 0–95

Bone marrow blasts, % 0.56
 Median 68 64
 Range 6–99 0–95

Extramedullary involvement, n (%) 7 (19) 4 (13) 0.53

NPM1, n (%) 0.003
 Mutated 28 (80) 15 (44)
 Wild type 7 (20) 19 (56)

FLT3-ITD, n (%) 0.005
 Mutated 8 (26) 20 (63)
  FLT3-ITD allelic raio ≥0.50 4 7
  FLT3-ITD allelic ratio <0.50 4 13
 Wild type 23 (74) 12 (38)

CEBPA, n (%) 1.00
 Biallelic mutations 1 (4) 0 (0)
 Wild type or monoallelic mutations 27 (96) 25 (100)

FLT3-TKD, n (%) 1.00
 Present 2 (6) 2 (6)
 Absent 32 (94) 31 (94)

WT1, n (%) 0.71
 Mutated 3 (9) 4 (12)
 Wild type 31 (91) 29 (88)

TET2, n (%) 0.59
 Mutated 11 (32) 8 (24)
 Wild type 23 (68) 25 (76)

IDH1, n (%) 0.75
 Mutated 5 (15) 6 (18)
 Wild type 29 (85) 27 (82)

IDH2, n (%) 0.51
 Mutated 4 (12) 6 (18)
 Wild type 30 (88) 27 (82)

ASXL1, n (%) 0.43
 Mutated 2 (6) 4 (12)
 Wild type 32 (94) 29 (88)

DNMT3A, n (%) 0.12
 Mutated 15 (44) 8 (24)
 Wild type 19 (56) 25 (76)

RUNX1, n (%) 0.03
 Mutated 1 (3) 7 (21)
 Wild type 33 (97) 26 (79)

ELN Risk Category,a n (%) <0.001
 Favorable 22 (79) 6 (23)
 Intermediate 5 (18) 9 (35)
 Adverse 1 (4) 11 (42)

ERG expression group,b n (%) <0.001
 High 11 (29) 27 (71)
 Low 27 (71) 11 (29)

BAALC expression group,b n (%) 0.003
 High 12 (32) 26 (68)
 Low 26 (68) 12 (32)

MN1 expression group,b n (%) 0.04
 High 24 (63) 14 (37)
 Low 14 (37) 24 (63)

miR-181a expression group,b n (%) 0.82
 High 20 (53) 18 (47)
 Low 18 (47) 20 (53)

miR-3151,b n (%) 0.82
 High 20 (53) 18 (47)
 Low 18 (47) 20 (53)

miR-155 expression group,b n (%) 0.04
 High 14 (37) 24 (63)
 Low 24 (63) 14 (37)

Abbreviations: n, number; WBC, white blood cell; ELN, European LeukemiaNet; FLT3-ITD, internal tandem duplication of the FLT3 gene; FLT3-TKD, tyrosine kinase domain mutation in the FLT3 gene.

a

Among patients with cytogenetically normal acute myeloid leukemia (CN-AML), the ELN Favorable Risk Category comprises patients with biallelic mutations in CEBPA and patients with mutated NPM1 without FLT3-ITD or with FLT3-ITDlow. The ELN Intermediate Risk Category includes patients with wild-type CEBPA and either wild-type NPM1 without FLT3-ITD, wild-type NPM1 and FLT3-ITDlow or mutated NPM1 and FLT3-ITDhigh. The ELN Adverse Risk Category comprises patients with wild-type CEBPA and wild-type NPM1 with FLT3-ITDhigh, patients with mutated TP53, and patients with mutated RUNX1 and/or mutated ASXL1 (if these mutations do not co-occur with Favorable-risk AML subtype). FLT3-ITDlow is defined by a FLT3-ITD/FLT3 wild-type allelic ratio of less than 0.5 and FLT3-ITDhigh is defined as by a FLT3-ITD/FLT3 wild-type allelic ratio of equal to or more than 0.5.

b

The median expression value was used as the cut point.