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. Author manuscript; available in PMC: 2019 Sep 1.
Published in final edited form as: Prostate. 2018 Apr 14;78(12):879–888. doi: 10.1002/pros.23535

Table V.

Factors associated with understanding of personal genetic test results among males undergoing multigene testing for suspected inherited prostate cancer

Discordance between self-reported vs. actual genetic test results p-value
No Yes
All 88 (100.0) 13 (100.0)
Site* 0.015
 Site 1 41 (46.6) 11 (84.6)
 Site 2 47 (53.4) 2 (15.4)
Age, Mean (SD) 62.6 (8.5) 62.5 (5.9) 0.941
Age, N (%) >0.999
 30–49 6 (6.8) 0 (0.0)
 50–64 43 (48.9) 7 (53.8)
 65–89 39 (44.3) 6 (46.2)
Race, N (%) >0.999
 Not answered 1 (1.1) 0 (0.0)
 White 73 (83.0) 11 (84.6)
 Black or African American 12 (13.6) 2 (15.4)
 Asian 1 (1.1) 0 (0.0)
 Multiracial 1 (1.1) 0 (0.0)
Education, N(%) 0.617
 Not answered 1 (1.1) 0 (0.0)
 Less than high school 1 (1.1) 0 (0.0)
 HS/GED or Vocational/Technical School 11 (12.5) 2 (15.4)
 Some College/Associate’s Degree 12 (13.6) 3 (23.1)
 Bachelor’s Degree or higher 63 (71.6) 8 (61.5)
Knowledge Score, Mean (SD) 10.1 (2.9) 9.0 (3.5) 0.283
Literacy Score, Mean (SD) 4.3 (0.7) 4.3 (0.7) 0.895
Numeracy Score, Mean (SD) 2.4 (0.8) 2.4 (1.0) 0.985
Prostate Cancer Diagnosis, N (%) 52 (59.1) 6 (46.2) 0.388
Age of Diagnosis, Mean (SD) 60.2 (6.3) 6 (60.2) 0.988
Age of Diagnosis, N (%) 0.354
 30–49 3 (5.8) 1 (16.7)
 50–64 34 (65.4) 3 (50.0)
 65–89 15 (28.8) 2 (33.3)
Family history of HCS, N (%) 41 (46.6) 2 (15.4) 0.039
Family History (FDRs), N (%)
 Cancer, any site 81 (92.0) 10 (76.9) 0.118
 Prostate 53 (60.2) 6 (46.2) 0.377
 Breast 27 (30.7) 2 (15.4) 0.338
 Ovarian 3 (3.4) 0 (0.0) >0.999
 Colon 12 (13.6) 3 (23.1) 0.404
 Pancreatic 3 (3.4) 0 (0.0) >0.999
Family History (any relative), N (%)
 Cancer, any site 84 (95.5) 11 (84.6) 0.171
 Prostate 66 (75.0) 7 (53.8) 0.180
 Breast 46 (52.3) 2 (15.4) 0.017
 Ovarian 14 (15.9) 0 (0.0) 0.205
 Colon 19 (21.6) 6 (46.2) 0.082
 Pancreatic 7 (8.0) 0 (0.0) 0.590
Genetic test result of VUS 18 (20.5) 12 (92.3) <0.001
*

Site 1 provided pretest counseling with a video + handout. Post-test disclosure was in-person for men with a mutation and by phone for men with a variant of uncertain significance or negative results. Site 2 provided pretest counseling and post-test disclosure in-person or by telehealth.