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Table 3 Genetic testing completion, results and use of information

From: Impact of a genetic counseling requirement prior to genetic testing

  

GC Requirement Policy

Total

N (%)

Before

N (%)

After

N (%)

P-value

BRCA1/2 Testing Completion

n = 1247

n = 297

n = 940

 

 Yes

966 (77.5%)

243 (81.5%)

723 (76.2%)

0.13

 No

271 (21.7%)

54 (18.1%)

217 (22.9%)

 Unknown/Missing/Declined

10 (0.8%)

1 (0.3%)

9 (1%)

BRCA1/2 Test Results

n = 966

n = 243

n = 723

 

 Mutation

89 (9.2%)

26 (10.7%)

63 (8.7%)

0.55

 No Mutation

821 (85.0%)

204 (84.0%)

615 (85.3%)

 Results Uncertain

19 (2.0%)

6 (2.5%)

13 (1.8%)

 Do not Understand Results

8 (0.8%)

0 (0.0%)

8 (1.1%)

 Unknown

8 (0.8%)

2 (0.8%)

6 (0.8%)

 Missing/Declined

21 (2.2%)

5 (2.1%)

16 (2.2%)

Most commonly reported use of genetic testing resultsa

n = 966

n = 243

n = 723

 

 Talked with Family Members about Results

590 (47.3%)

147 (60.5%)

443 (61.3%)

0.42

 Routine Breast Cancer Screenings

329 (26.4%)

71 (29.2%)

258 (35.7%)

0.25

 Plan Cancer Treatment

173 (13.9%)

42 (17.3%)

131 (18.1%)

0.90

 Additional Breast Cancer Screening with MRI utilized

53 (4.3%)

10 (4.1%)

43 (6.0%)

0.38

 Surgery to Remove Breast or Ovaries to prevent Cancer

40 (3.2%)

11 (4.5%)

29 (4.0%)

0.59

 Other

39 (3.1%)

17 (7.0%)

22 (3.0%)

0.003

Most commonly reported reasons for why BRCA1/2 testing was not completeda

n = 271

n = 54

n = 217

 

 Insurance issues/requirements

165 (60.9%)

39 (72.2%)

126 (58.1%)

0.06

 Costs

129 (47.6%)

38 (70.4%)

91 (41.9%)

0.0002

 Testing not recommended by GC

56 (20.7%)

3 (5.6%)

53 (24.4%)

0.002

 Testing recommended for another family member

24 (8.9%)

4 (7.4%)

20 (9.2%)

0.79

 Likelihood low so decided against testing

18 (6.6%)

1 (1.9%)

17 (7.8%)

0.14

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