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. 2023 Jan 23;128(7):1360–1368. doi: 10.1038/s41416-023-02141-0

Table 2.

Univariable and multivariable analysis of clinicopathological and molecular features in high-risk endometrial cancer patients.

Recurrence Univariable analysis Multivariable analysis
n = 643, 207 events HR 95% CI p-value HR 95% CI p-value
Age
  ≤60 years 1 1
  >60 years 1.97 1.43–2.72 <.001 1.43 1.02–2.01 0.037
Stage
  I 1 1
  II 1.09 0.74–1.63 0.66 1.78 1.15–2.75 0.009
  III 2.14 1.52–3.00 <.001 3.47 2.37–5.07 <.001
Histology and grade
  Endometrioid, low-grade 1 1
  Endometrioid, high-grade 1.12 0.79–1.60 0.52 1.48 0.98–2.23 0.06
  Non-endometrioid 1.60 1.16–2.19 0.004 1.47 0.96–2.26 0.08
LVSI
  Absent 1 1
  Present 1.53 1.13–2.06 0.006 1.32 0.97–1.79 0.08
Treatment received
  RT (VBT or EBRT) 1 1
  RT (VBT or EBRT) + CT 0.81 0.58–1.13 0.21 0.65 0.47–0.91 0.012
Molecular subgroups
  MMRd 1 1
  POLEmut 0.09 0.02–0.38 0.001 0.11 0.03–0.46 0.002
  NSMP 1.00 0.70–1.43 0.99 0.97 0.66–1.42 0.87
  p53abn 2.30 1.65–3.21 <.001 2.43 1.65–3.57 <.001

Model fit multivariable model: Akaike’s information criterion (AIC) 2173.77, model concordance (C-index) 0.712. Bootstrap resampling model validation: C-index re-estimation 0.72.

HR hazard ratio, CI confidence interval, LVSI lymphovascular space invasion, RT radiotherapy, VBT vaginal brachytherapy, EBRT external beam radiotherapy, CT chemotherapy, MMRd mismatch repair-deficient, POLEmut POLE ultra-mutated, p53abn p53-abnormal, NSMP no specific molecular profile, IHC immunohistochemistry.