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. 2021 Apr 14;55(3):202–211. doi: 10.4132/jptm.2021.02.19

Table 2.

The association between D-MMR EC and clinicopathological characteristics

Clinicopathological characteristics in EC Pooled % portion (95% CI) No. of studies I2 (95% CI, %) p-value Model
Overall D-MMR mutation 24.477 (21.022–28.106) 25 91.890 (89.250–93.880) < .001 Random effect
D-MMR mutation in type I 25.810 (22.503–29.261) 14 80.440 (68.080–88.020) < .001 Random effect
D-MMR mutation in type II 13.736 (8.392–20.144) 10 77.320 (58.360–87.650) < .001 Random effect
Stage I–II 79.430 (71.500–86.357) 6 68.640 (25.980–86.710) .007 Random effect
Stage III–IV 20.168 (13.746–27.469) 6 61.850 (7.020–84.350) .022 Random effect
Grade I–II 65.718 (52.602–77.714) 10 91.700 (86.860–94.760) < .001 Random effect
Grade III 21.529 (15.930–27.718) 10 94.050 (90.97–96.08) < .001 Random effect
Lymphovascular invasion 32.105 (21.371–43.896) 10 91.380 (86.270–94.590) < .001 Random effect
MI less than 50% 51.807 (38.514–64.971) 8 89.860 (82.410–94.150) < .001 Random effect
MI more than 50% 42.346 (28.576–56.750) 8 91.360 (85.380–94.890) < .001 Random effect

D-MMR, mismatch repair deficiency; EC, endometrial carcinoma; CI, confidence interval; MI, myometrial invasion.