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. 2015 Sep 1;107(11):djv249. doi: 10.1093/jnci/djv249

Table 1.

Clinicopathologic characteristics of patients with both CTCF and ZFHX3 defects and women with no detectable abnormalities*

Clinicopathologic feature CTCF and ZFHX3 defects (23.3%)(n = 109)
No. (%)
Wild-type (51.0%)(n = 238)
No. (%)
P
Grade
 1 43 (39.8) 139 (58.4) .001
 2 33 (30.6) 70 (29.4)
 3 32 (29.6) 29 (12.2)
Age, y
 <60 32 (29.4) 105 (44.1) .04
 >60 77 (70.6) 133 (55.9)
LVSI
 Present 46 (44.2) 70 (29.9) .04
 Absent 58 (55.8) 164 (70.1)
Stage
 Early: I & II 90 (82.6) 194 (81.9) ns
 Advanced: III & IV 19 (17.4) 43 (18.1)
Adjuvant therapy
 Yes 39 (36.1) 66 (27.7) ns
 No 69 (63.9) 172 (72.3)
BMI, kg/m2
 <30 35 (38.9) 71 (33.0) ns
 >30 55 (61.1) 144 (67.0)
Race
 White 89 (81.7) 209 (87.8) ns
 Nonwhite 20 (18.3) 29 (12.2)
Events‡
 Recur/progress 23 of 107 (21.5) 28 of 232 (12.1)
 Death 51 of 107 (47.7) 77 of 232 (33.2)

* Defects include samples with mutation or loss of heterozygosity. Forty-six cases uninformative for mutation/loss of heterozygosity status and 29 cases with POLE mutations were excluded. BMI = body mass index; LVSI = lymphovascular space invasion; ns = not significant.

† Significance of grade was determined by chi-squared test. Significance of other variables was determined by Fisher’s exact test. All P values are two-tailed and false discovery rate–adjusted.

‡ Excludes perioperative deaths.