Skip to main content
. 2015 Nov 13;108(2):djv323. doi: 10.1093/jnci/djv323

Table 4.

Patient characteristics for tet2-DMC–low and –high in the TCGA dataset*

Characteristics tet2-DMC–low tet2-DMC–high P
Total No. 48 146
Age, mean (range), y 49 (21–76) 57 (18–88) .0011
Male sex, No. (%) 25 (52) 80 (55) .87
Bone marrow blasts at diagnosis, mean (range), % 30 (0–94) 39 (0–98) .07
WBC at diagnosis, mean (range), 103/uL 29 (1–134) 41 (1–298) .16
Cytogenetic risk group, No. (%) <.0001
Favorable 31 (67) 5 (3)
Intermediate 14 (30) 99 (68)
Poor 1 (2) 41 (28)
Acute promyelocytic leukemia (M3), No. (%) 18 (38) 1 (1) <.0001
Overall survival, median (range), mo 55 (0–85+) 15 (0–95+) .0003
Mutations, No. (%)
ASXL1 0 (0) 3 (6) 1
DNMT3A 2 (12) 17 (31) .13
FLT3-TKD 17 (35) 40 (29) .47
RAS 2 (4) 9 (6) .73
NPM 8 (17) 37 (26) .24
IDH1 1 (2) 17 (12) .08
IDH2 0 (0) 17 (12) .008
TET2 0 (0) 8 (15) .18
TET2/IDH 1 (2) 41 (28) <.0001

* The P values were computed from Fisher’s exact test for two-by-two contingency analyses, Mann-Whitney test to compare continuous variables (age, bone marrow blasts at diagnosis, and WBC at diagnosis), and the log-rank test for survival data. All P values were two-tailed, and the threshold of statistical significance was P < .05. TCGA = the Cancer Genome Atlas; tet2-DMCs = TET2-specific differentially methylated CpGs.