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. 2019 Nov 21;24(1):1067–1075. doi: 10.1111/jcmm.14831

Table 1.

Clinical and molecular characteristics of patients in different treatment groups

Characteristics Chemotherapy‐only group Allo‐HSCT group
High DDIT4 (n = 42) Low DDIT4 (n = 42) P High DDIT4 (n = 35) Low DDIT4 (n = 36) P
Age/years, median (range) 70 (35‐88) 63 (22‐82) .003a 53 (18‐72) 50 (21‐65) .411a
Age group/n (%)
<60 y 8 (19.0) 18 (42.9) .018b 23 (65.7) 29 (80.6) .158b
≥60 y 34 (81.0) 24 (57.1)   12 (34.3) 7 (19.4)  
Gender/n (%)
Male 25 (59.5) 20 (47.6) .274b 20 (57.1) 21 (58.3) .919b
Female 17 (40.5) 22 (52.4)   15 (42.9) 15 (41.7)  
WBC/×109/L, median (range) 13.3 (1.0‐297.4) 16.1 (0.7‐171.9) .522a 34.2 (0.6‐223.8) 29.4 (0.9‐115.4) .761a
BM blast/%, median (range) 77 (32‐99) 66 (30‐95) .041a 72 (30‐100) 70 (34‐99) .913a
PB blast/%, median (range) 22 (0‐98) 25 (0‐91) .449a 53 (0‐96) 45 (0‐94) .366a
FAB subtypes/n (%)
M0 7 (16.7) 0 (0.0) .012b 4 (11.4) 5 (13.9) .755b
M1 10 (23.8) 10 (23.8) 1.000b 17 (48.6) 6 (16.7) .004b
M2 7 (16.7) 14 (33.3) .078b 9 (25.7) 9 (25.0) 1.000b
M3 0 (0.0) 0 (0.0) 1.000b 0 (0.0) 1 (2.8) .493b
M4 8 (19.0) 12 (28.6) .306b 1 (2.9) 12 (33.3) .001b
M5 6 (14.3) 6 (14.3) 1.000b 2 (5.7) 2 (5.6) 1.000b
M6 1 (2.4) 0 (0.0) 1.000b 1 (2.9) 0 (0.0) .493b
M7 3 (7.1) 0 (0.0) .241b 1 (2.9) 1 (2.8) 1.000b
Cytogenetics/n (%)
Normal 19 (45.2) 21 (50.0) .662b 18 (51.4) 15 (41.7) .410b
Complex karyotype 9 (21.4) 2 (4.8) .048b 9 (25.7) 2 (5.6) .019b
8 Trisomy 0 (0.0) 0 (0.0) 1.000b 3 (8.6) 3 (8.3) 1.000b
inv(16)/CBFβ‐MYH11 0 (0.0) 6 (14.3) .026b 0 (0.0) 5 (13.9) .054b
11q23/MLL 1 (2.4) 2 (4.8) .614b 1 (2.9) 2 (5.6) 1.000b
−7/7q‐ 2 (4.8) 1 (2.4) .614b 2 (5.7) 1 (2.8) .614b
t(15;17)/PML‐RARA 0 (0.0) 0 (0.0) 1.000b 0 (0.0) 1 (2.8) 1.000b
t(9;22)/BCR‐ABL1 1 (2.4) 0 (0.0) 1.000b 1 (2.9) 1 (2.8) 1.000b
t(8;21)/RUNX1‐RUNX1T1 0 (0.0) 6 (14.3) .026b 0 (0.0) 1 (2.8) 1.000b
Others 10 (23.8) 4 (9.5) .079b 1 (2.9) 5 (13.9) .199b
Risk/n (%)
Good 0 (0.0) 12 (28.6) .000b 0 (0.0) 7 (19.4) .011b
Intermediate 26 (61.9) 20 (47.6) .188b 19 (54.3) 21 (58.3) .731b
Poor 16 (38.1) 10 (23.8) .157b 16 (45.7) 8 (22.2) .036b
FLT3‐ITD/n (%)
Positive 6 (14.3) 9 (21.4) .393b 9 (25.7) 8 (22.2) .730b
Negative 36 (85.7) 33 (78.6)   26 (74.3) 28 (77.8)  
NPM1/n (%)
Mutation 13 (31.0) 14 (13.3) .815b 9 (25.7) 9 (25.0) .945b
Wild type 29 (69.0) 28 (66.7)   26 (74.3) 27 (75.0)  
DNMT3A/n (%)
Mutation 12 (28.6) 11 (26.2) .807b 10 (28.6) 7 (19.4) .368b
Wild type 30 (71.4) 31 (73.8)   25 (71.4) 29 (80.6)  
IDH1/IDH2/n (%)
Mutation 9 (21.4) 6 (14.3) .393b 11 (31.4) 6 (16.7) .145b
Wild type 33 (78.6) 36 (85.7)   24 (68.6) 30 (83.3)  
RUNX1/n (%)
Mutation 12 (28.6) 2 (4.8) .003b 3 (8.6) 5 (13.9) .710b
Wild type 30 (71.4) 42 (95.2)   32 (91.4) 31 (86.1)  
NRAS/KRAS/n (%)
Mutation 6 (14.3) 6 (14.3) 1.000b 1 (2.9) 6 (16.7) .107b
Wild type 36 (85.7) 36 (85.7)   34 (97.1) 30 (83.3)  
TET2/n (%)
Mutation 4 (9.5) 7 (16.7) .332b 0 (0.0) 4 (11.1) .115b
Wild type 38 (90.5) 35 (83.3)   35 (100) 32 (88.9)  
TP53/n (%)
Mutation 9 (21.4) 2 (4.8) .024b 3 (8.6) 1 (2.8) .357b
Wild type 33 (78.6) 40 (95.2)   32 (91.4) 35 (97.2)  

Abbreviations: BM, bone marrow; FAB, French‐American‐British; PB, peripheral blood; WBC, white blood cell.

a

Denotes Mann‐Whitney U test

b

Denotes chi‐square test.