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. 2020 Jan 30;19(2):133–142. doi: 10.1007/s10689-020-00160-x

Table 3.

Genetic testing of all patients and evaluation of criteria

Innlandet hospital (n = 162) Ahus (n = 199) Combined (n = 361)
Genetic testing
 Offered genetic testing

n = 161a

48 (29.8%)

n = 195a

83 (42.6%)

n = 356a

131 (36.8%)

 Tested

n = 161a

45 (27.8%)

n = 195a

80 (40.2%)

n = 356a

125 (34.6%)

 Uptake of genetic testing

n = 48

45 (93.8%)

n = 83

80 (96.4%)

n = 131

125 (95.4%)

 Test ordered by n = 45 n = 80 n = 125
  Surgeon 23 (51.1%) 48 (60%) 71 (56.8%)
  Oncologist 22 (48.9%) 31 (38.8%) 53 (42.4%)
  Other 1 (1.3%) 1 (0.8%)
Evaluation of family history
 Asked about family history of cancer

n = 162

126 (77.8%)

n = 199

189 (95.0%)

n = 361

315 (87.3%)

 Reported family history of breast and/or ovarian cancer

n = 126

58 (46.0%)

n = 189

66 (34.9%)

n = 315

124 (39.4%)

Criteria fulfilled
 BC < 50 years

n = 162

29 (17.9%)

n = 199

31 (15.6%)

n = 361

60 (16.6%)

 Bilateral BC < 60 years

n = 162

2 (1.2%)

n = 199

2 (1%)

n = 361

4 (1.1%)

 TNBC < 60 years

n = 162

3 (1.9%)

n = 199

3 (1.5%)

n = 361

6 (1.7%)

 Male breast cancer

n = 199

2 (1.0%)

n = 361

2 (0.5%)

 Family history of BC and/or OCb

n = 126

18 (14.3%)

n = 189

6 (3.2%)

n = 315

24 (7.6%)

aExcluded patients who had been tested prior to their breast cancer diagnosis

bThese patients were 50 years or older at time of diagnosis, and did not fulfill any of the other criteria (TNBC < 60 years, bilateral B < 60 years or male BC)