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. 2016 Apr 21;7(22):33179–33191. doi: 10.18632/oncotarget.8891

Table 1. Patent characteristics.

All patients (N=773) Patients on ADs (n=203) Patients on SSRIs (n=125)
Characteristic No. % No. % No. %
Age (years)
  Median 60.1 59.0 59.7
  IQR 52-68 50.3-67 51-67
FU duration, months
  Median 54.8 58.8 62.5
  IQR 31.4-85.3 33.5-83.2 37.7-83.2
Race
  White 679 91.6 183 97.3 115 97.5
  Other 62 8.4 5 2.7 3 2.5
Stage
  I 78 10.2 23 11.3 16 12.8
  II 60 7.8 15 7.4 10 8.0
  III 549 71.9 147 72.4 88 70.4
  IV 77 10.1 18 8.9 11 8.8
Residual Disease
  Optimal 492 63.7 140 69.0 87 69.6
  Suboptimal 281 36.4 63 31.0 38 30.4
Grade
  High 627 81.4 173 85.2 105 84.0
  Low 143 18.6 30 14.8 20 16.0
Histology
  Serous 582 75.5 155 76.4 93 74.4
  Other 189 24.5 48 23.6 32 25.6
ADs 203 26.3 203 100.0 125 100.0
SSRIs 125 16.2 125 61.6 125 100.0
SNRIs 44 5.7 44 21.7 7 5.6
TCAs 24 3.1 24 11.8 3 2.4
NDRIs 18 2.3 18 8.9 5 4.0
SARIs 11 1.4 11 5.4 3 2.4
NaSSAs 9 1.2 9 4.4 3 2.4

Abbreviations: ADs, antidepressants; FU, follow-up; IQR, interquartile range; NaSSAs, noradrenergic and specific serotonergic antidepressants; NDRIs, norepinephrine-dopamine reuptake inhibitors; SARIs, serotonin antagonist-reuptake inhibitors; SNRIs, selective norepinephrine-reuptake inhibitors; SSRIs, selective serotonin-reuptake inhibitors; TCAs, tricyclic antidepressants.