Table 1.
Trial centre | Total | ||
---|---|---|---|
Tampere | Helsinki | ||
Invited, N | 200 | 199* | 399 |
Consented, N (%) † | 85 (43) | 85 (43) | 170 (43) |
Previous PSA, N (%) ‡ | 61 (72) | 51 (61) | 112 (66) |
Previous prostate biopsy, N ‡ | 2 (2) | 5 (6) | 7 (4) |
Blood sample obtained, N (%) † | 81 (41) | 77 (39) | 158 (40) |
PSA ≥3 ng/mL, N (%) ‡ | 13 (16) | 14 (18) | 27 (17) |
Median PSA in men with PSA ≥3 ng/mL, ng/mL | 4.4 | 5.5 | 5.0 |
Kallikrein panel ≥7.5%, N (%) ‡ | 9 (69) | 13 (93) | 22 (81) |
mpMRI negative/PI‐RADS v2 score <3, N (%) ‡ | 6 (67) | 6 (46) | 12 (55) |
mpMRI suspect | |||
PI‐RADS v2 score 3, N (%) | 2 (22) | 2 (15) | 4 (18) |
PI‐RADS v2 score 4/5 | 1 (11) | 5 (38) | 6 (27) |
Prostate cancer cases detected, N (%) | 2 (67) | 5 (71) | 7 (70) |
Prostate cancer, Gleason sum 6 | 2 (67) | 0 (0) | 2 (20) |
Prostate cancer, Gleason sum 7+ | 0 (0) | 5 (100) | 5 (50) |
mpMRI, multiparametric MRI; PI‐RADS, Prostate Imaging Reporting and Data System.
1 person was excluded from the invitation list because of sex change.
Proportion out of invited men.
Proportion out of men with information available, i.e. those who were included that stage of the screening protocol from PSA to kallikrein panel to MRI to biopsy.