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. 2020 May 18;11(15):4581–4588. doi: 10.7150/jca.44766

Table 2.

Comparison of clinical and molecular characteristics in different SPNS2/3 expression groups among chemotherapy-only group.

Characteristics SPNS2 P SPNS3 P
High (n=42) Low (n=42) High (n=42) Low (n=42)
Age (years), median (range) 67.5 (25-88) 66 (22-81) 0.975a 66 (33-88) 67 (22-81) 0.982a
Age group, n (%) 0.814b 0.814b
<60 years 12 (28.6) 14 (33.3) 14 (33.3) 12 (28.6)
≥60 years 30 (71.4) 28 (66.7) 28 (66.7) 30 (71.4)
Gender, n (%) 0.662b 0.382b
Male 21 (50.0) 24 (57.1) 25 (59.5) 20 (47.6)
Female 21 (50.0) 18 (42.9) 17 (40.5) 22 (52.4)
WBC (×109/L),
median (range)
14.8
(0.7-297.4)
14.6
(1.9-131.5)
0.862a 16.5
(0.7-134.4)
13.3
(1.0-297.4)
0.943a
BM blasts (%), median (range) 73.5
(32-99)
69.5
(30-95)
0.455a 74
(30-98)
68
(32-99)
0.785a
PB blasts (%), median (range) 49.5
(0-98)
7.5
(0-90)
0a 38
(0-97)
17.5
(0-98)
0.149a
FAB subtypes, n (%)
M0 6 (14.3) 1 (2.4) 0.109b 3 (7.1) 4 (9.5) 1.000b
M1 18 (42.9) 2 (4.8) 0b 13 (31.0) 7 (16.7) 0.200b
M2 13 (31.0) 8 (19.0) 0.314b 9 (21.4) 12 (28.6) 0.615b
M4 4 (9.5) 16 (38.1) 0.004b 12 (28.6) 8 (19.0) 0.443b
M5 1 (2.4) 11 (26.2) 0.003b 4 (9.5) 8 (19.0) 0.350b
M6 0 (0.0) 1 (2.4) 1.000b 1 (2.4) 0 (0.0) 1.000b
M7 0 (0.0) 2 (4.8) 0.494b 0 (0.0) 2 (4.8) 0.494b
Cytogenetics, n (%)
Normal 19 (45.2) 21 (50.0) 0.827b 22 (52.4) 18 (42.9) 0.512b
t(9;22)/BCR-ABL1 0 (0.0) 1 (2.44) 1.000b 0 (0.0) 1 (2.4) 1.000b
inv(16)/CBFβ-MYH11 1 (2.4) 5 (11.9) 0.202b 2 (4.8) 4 (9.5) 0.676b
Complex 7 (16.7) 5 (11.9) 0.520b 7 (16.7) 4 (9.5) 0.520b
11q23/MLL 1 (2.4) 2 (4.8) 1.000b 2 (4.8) 1 (2.4) 1.000b
t(8;12)/RUNX1-RUNX1T1 3 (7.1) 3 (7.1) 1.000b 0 (0.0) 6 (14.3) 0.026b
Others 11 (26.2) 6 (14.3) 0.277b 9 (21.4) 8 (19.0) 1.000b
Risk, n (%)
Good 4 (9.5) 8 (19.0) 0.350b 2 (4.8) 10 (23.8) 0.026b
Intermediate 24 (57.1) 27 (64.3) 0.655b 27 (64.3) 24 (57.1) 0.655b
Poor 12 (28.6) 7 (16.7) 0.297b 11 (26.2) 8 (19.0) 0.603b
FLT3, n (%) 0.668b 0.447b
FLT3-ITD 6 (4.3) 9 (21.4) 8 (19.0) 7 (16.7)
FLT3-TKD 9 (9.5) 3 (7.1) 5 (11.9) 2 (4.8)
Wildtype 32 (76.2) 30 (71.4) 29 (69.0) 33 (78.6)
NPM1, n (%) 0.641b 0.160b
Mutation 15 (35.7) 12 (28.6) 17 (40.5) 10 (23.8)
Wildtype 27 (64.3) 30 (71.4) 25 (59.5) 32 (76.2)
DNMT3A, n (%) 0.625b 0.141b
Mutation 13 (31.0) 10 (23.8) 15 (35.7) 8 (19.0)
Wildtype 29 (69.0) 32 (76.2) 27 (64.3) 34 (81.0)
IDH1/IDH2, n (%) 0.570b 1.000b
Mutation 9 (21.4) 6 (14.3) 7 (16.7) 8 (19.0)
Wildtype 33 (78.6) 36 (85.7) 35 (83.3) 34 (81.0)
RUNX1, n (%) 0.713b 1.000b
Mutation 5 (11.9) 3 (7.1) 4 (9.5) 4 (9.5)
Wildtype 37 (88.1) 39 (92.9) 38 (90.5) 38 (90.5)
NRAS/KRAS, n (%) 0.756b 0.756b
Mutation 5 (11.9) 7 (16.7) 5 (11.9) 7 (16.7)
Wildtype 37 (88.1) 35 (83.3) 37 (88.1) 35 (83.3)
TET2, n (%) 0.194b 1.000b
Mutation 8 (19.0) 3 (7.1) 5 (11.9) 6 (14.3)
Wildtype 34 (81.0) 39 (92.9) 37 (88.1) 36 (85.7)
TP53, n (%) 1.000b 0.520b
Mutation 5 (11.9) 6 (14.3) 7 (16.7) 4 (9.5)
Wildtype 37 (88.1) 36 (85.7) 35 (83.3) 38 (90.5)
Relapse/n (%) 0.261b 0.822b
Yes 13 (31.0) 19 (45.2) 15 (37.5) 17 (40.5)
No 29 (69.0) 23 (54.8) 27 (64.3) 25 (59.5)

WBC white blood cell, BM bone marrow, PB peripheral blood, FAB French American British

aMann-Whitney U-test

bChi-square test