Table 1.
n | % | |
---|---|---|
Gender | ||
Female | 172 | 98.3% |
Male | 3 | 1.7% |
Ethnicity | ||
African American | 36 | 20.6% |
Asian | 3 | 1.7% |
Latino/a | 19 | 10.9% |
White | 115 | 65.7% |
Other/unknown | 2 | 1.1% |
Insurance status | ||
Private | 140 | 80.0% |
Medicaid | 4 | 2.3% |
Medicare or Veterans Affairs | 25 | 14.3% |
No insurance | 6 | 3.4% |
Age at diagnosis (years) | ||
≤45 | 91 | 52.0% |
46–49 | 12 | 6.9% |
50–59 | 31 | 17.7% |
60–69 | 18 | 10.3% |
≥70 | 23 | 13.1% |
Genetic test type | ||
No test performed | 38 | 21.7% |
BRCA 1/2 testing only | 23 | 13.1% |
Multigene panel | 114 | 65.1% |
Genetic test outcome | ||
Not tested | 38 | 21.7% |
Negative | 104 | 59.4% |
Variant of unknown significance only | 17 | 9.7% |
Pathogenic mutation | 16 | 9.1% |
Genetic discussion modality | ||
Formal counseling (genetic counselor) | 124 | 70.9% |
Physician-directed discussion | 7 | 4.0% |
No counseling | 44 | 25.1% |