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. 2017 Feb 9;8(16):25928–25941. doi: 10.18632/oncotarget.15237

Table 1. VPC prostate cancer cohort clinical details.

VPC ID Tumour or Benign Age at Dx PSA at Dx Gleason score PSA recurrence months to Follow up (months post-surgery) ETS status
VPCT1 T 74 2.1 9 (4+5) N 123 ERG
VPCT4 T 65 17.0 9 (4+5) Y (nrn) 71 negative
VPCB4 B n/a
VPCT5 T 71 8.0 8 (4+4) Y (34) 94 ERG
VPCT11 T 65 8.1 7 (3+4) N 83 ERG
VPCB11 B n/a
VPCT12 T 64 1.37 9 (4+5) Y (30) 66 ETV1
VPCT13 T 57 31.0 9 (4+5) Y (28) 48 ERG
VPCB13 B n/a
VPCT15 T 69 15.07 7 (4+3) Y (nrn) 41 negative
VPCT16 T 45 6.3 10 (5+5) Y (3) 45 negative
VPCT18 T 59 10.1 8 (4+4) Y (15) 46 ETV1
VPCT19 T 53 7.7 8 (4+4) N 18 (LTFU) ERG
VPCT21 T 70 65.3 9 (4+5) Y (nrn) 5 (LTFU) ERG
VPCT22 T 47 4.2 9 (5+3) Y (55) 59 ERG
VPCT23 T 63 22 10 (5+5) Y (nrn) 40 ETV1
VPCT24 T 64 17 9 (5+4) Y (nrn) 49 ERG

The prostate cancer cohort of the Vancouver Prostate Centre (VPC) consisted of 14 untreated primary tumours and 3 matched benign prostate tissues [44]. Abbreviations: T, tumour; B, Benign; Dx, diagnosis; PSA, prostate specific antigen; nrn, never reached nadir; N, no; Y, yes; LTFU, lost to follow-up. There were no differences in stromal content across the cohort based on comparisons of desmin and vimentin expression (fibroblasts) [44].