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Table 3 Questions regarding the experiences with recontacting for the additional CHEK2 mutation test

From: Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences

 

CHEK2 c.1100del PV

No CHEK2 c.1100del PV detected

Total

N = 52

N = 104

Questions regarding recontacting

N

%

N

%

p-value

Recontact appreciated

 agree

51

98.1%

99

95.2%

n.s.

 neutral

1

1.9%

5

4.8%

 disagree

0

0.0%

0

0.0%

Recontacting caused a lot of anxiety for myself

 agree

6

11.5%

6

5.8%

n.s.

 neutral

12

23.1%

12

11.7%

 disagree

34

65.4%

85

82.5%

Recontacting increased my worries for the family

 agree

8

15.4%

2

1.9%

< 0.001

 neutral

17

32.7%

4

3.9%

 disagree

27

51.9%

97

94.2%

Written information sufficient for informed decision

 agree

50

96.2%

99

96.1%

n.s.

 neutral

1

1.9%

3

2.9%

 disagree

1

1.9%

1

1.0%

The decision for additional CHEK2 genetic testing was difficult

 agree

2

3.8%

2

1.9%

n.s.

 neutral

3

5.8%

7

6.7%

 disagree

47

90.4%

95

91.3%

Difficult to determine advantages and disadvantages of additional testing

 agree

5

9.6%

8

7.7%

n.s.

 neutral

7

13.5%

20

19.2%

 disagree

40

76.9%

76

73.1%

After receiving the CHEK2 test results

    

p-value

The results of the test were as expected

 agree

15

28.8%

39

39.0%

0.004

 neutral

19

36.5%

49

49.0%

 disagree

18

34.6%

12

12.0%

In retrospect I felt satisfied with having the choice for CHEK2 PV testing

 agree

51

98.1%

97

96.0%

n.s.

 neutral

1

1.9%

4

4.0%

 disagree

0

0.0%

0

0.0%

The test results influenced cancer worries counselee

 no change in cancer worries

35

67.3%

89

88.1%

< 0.001

 yes, increase of cancer worries

14

26.9%

1

1.0%

 yes, decrease of cancer worries

3

5.8%

11

10.9%

The test results influenced cancer worries family members

 no change in cancer worries

22

42.3%

81

80.2%

< 0.001

 yes, increase of cancer worries

27

51.9%

0

0.0%

 yes, decrease of cancer worries

3

5.8%

20

19.8%

Regrets about the choice for additional genetic testing

 disagree

52

100.0%

103

99.0%

n.s.

 neutral

0

0.0%

1

1.0%

 agree

0

0.0%

0

0.0%

Satisfaction with recontacting

 good

51

98.1%

103

99.0%

n.s.

 fair

1

1.9%

1

1.0%

 poor

0

0.0%

0

0.0%

Satisfaction with information prior to DNA-test

 good

46

88.5%

97

97.1%

n.s.

 fair

4

7.7%

3

2.9%

 poor

2

3.8%

0

0.0%

Satisfaction with information after test results

 good

49

94.2%

97

93.3%

n.s.

 fair

3

5.8%

7

6.7%

 poor

0

0.0%

0

0.0%