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. 2020 Sep 2;54(6):471–479. doi: 10.4132/jptm.2020.07.23

Table 2.

The association between POLE mutated EC and clinicopathology characteristics

Clinicopathological characteristics in EC Pooled % portion (95% CI, %) No. of studies I2 (95% CI) p-value Model
Overall POLE mutation 8.59 (7.01–10.32) 25 78.10 (68.15–84.94) < .001 Random effect
POLE mutation in type I 8.22 (6.27–10.42) 9 74.88 (51.43–87.00) < .001 Random effect
POLE mutation in type II 0.93 (0.34–1.81) 10 75.32 (54.08–86.74) < .001 Random effect
Stage I–II 89.51 (81.11–95.66) 10 69.09 (40.43–83.96) < .001 Random effect
Stage III–IV 14.77 (5.99–26.59) 7 65.96 (23.79–84.79) < .001 Random effect
Grade I–II 46.36 (30.66–62.43) 7 82.15 (64.34–91.06) < .001 Random effect
Grade III 51.53 (36.08–66.84) 8 81.79 (65.23–90.46) < .001 Random effect
Lymphovascular invasion 31.11 (10.44–56.86) 8 93.34 (89.15–95.91) < .001 Random effect
Myometrial invasion less than 50% 49.90 (43.71–56.21) 7 22.10 (0.00–65.16) 0.260 Fixed effect

POLE, DNA polymerase epsilon; EC, endometrial carcinoma; CI, confidence interval.