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. Author manuscript; available in PMC: 2023 Aug 1.
Published in final edited form as: Eur Urol. 2021 Dec 31;82(2):163–169. doi: 10.1016/j.eururo.2021.12.011

Table 1 –

Characteristics of the Prostate Biopsy Collaborative Group cohort, and among the four sites (Zurich, UTHSCSA, San Juan VA, and Durham VA) with additional family history data availablea

Characteristic Overall (N = 20 323) Detailed family history available (N = 4621)

Age at biopsy (yr) 65 (60–70) 65 (60–69)
 Missing 2 0
Race
 White 11 505 (80) 2605 (56)
 Black 2128 (15) 1779 (39)
 Other 708 (4.9) 229 (5.0)
 Missing 5982 8
Prostate-specific antigen (ng/ml) 6.4 (4.6, 9.8) 6.0 (4.6, 8.7)
Abnormal digital rectal exam 4474 (25) 1507 (34)
 Missing 2482 217
Prior negative biopsy 2798 (21) 924 (20)
 Missing 6933 0
Biopsy Gleason grade group
 Negative 9552 (47) 2089 (45)
 1 3682 (18) 925 (20)
 2 3185 (16) 770 (17)
 3 1491 (7.3) 365 (7.9)
 Gleason 7 unspecified 159 (0.8) 0 (0)
 4 924 (4.5) 247 (5.3)
 5 1330 (6.5) 225 (4.9)
MRI-guided biopsy 1234 (6.1) 318 (6.9)
First-degree prostate cancer family history 2889 (18) 888 (19)
 Missing 4524 2
Type of first-degree prostate cancer family history
 Father 446 (50)
 Brother 352 (40)
 Father and brother 83 (9.4)
 Son 6 (0.7)
 Missing 3
Number of first-degree prostate cancer relatives
 1 751 (85)
 2 108 (12)
 3 24 (2.7)
 4 4 (0.5)
 Missing 3
Second-degree prostate cancer family history 371 (8.0)
 Missing 6
First-degree breast cancer family history 348 (7.5)
 Missing 8

IQR = interquartile range; MRI = magnetic resonance imaging; UTHSCSA = University of Texas Health Science Center at San Antonio; VA = Veterans Affairs.

a

Additional data collected at these sites include the number of first- and second-degree relatives with a family history of prostate or breast cancer. Median (IQR) and n (%) are shown for continuous and categorical variables, respectively.