Table 2 Patient characteristics by pathogenic variant status overall and by gene.

From: Risk of lymphoid malignancy associated with cancer predisposition genes

 

No Mutation (N = 6788)

Any Mutation (N = 202)

ATM (N = 57)

CHEK2 (N = 125)

TP53 (N = 20)

Age

N

6660

202

57

125

20

 Median

63

63

64

62

61

 Range

18.0–94.0

20.0–90.0

25.0–90.0

20.0–89.0

37.0–79.0

Age category, N (%)

 Missing

4

0

0

0

0

 <60

2721 (40.1%)

83 (41.1%)

20 (35.1%)

54 (43.2%)

9 (45.0%)

 60+

4063 (59.9%)

119 (58.9%)

37 (64.9%)

71 (56.8%)

11 (55.0%)

Sex, N (%)

 Missing

3

0

0

0

0

 Female

2812 (41.4%)

85 (42.1%)

20 (35.1%)

59 (47.2%)

6 (30.0%)

 Male

3973 (58.6%)

117 (57.9%)

37 (64.9%)

66 (52.8%)

14 (70.0%)

Family history of hematologic malignancy, N (%)

 Missing

2162

66

19

37

10

 No

3945 (85.3%)

108 (79.4%)

31 (81.6%)

68 (77.3%)

9 (90.0%)

 Yes

681 (14.7%)

28 (20.6%)

7 (18.4%)

20 (22.7%)

1 (10.0%)

Personal history of prior solid tumor cancer, N (%)

 Missing

3376

100

27

63

10

 No

2881 (84.4%)

82 (80.4%)

27 (90.0%)

48 (77.4%)

7 (70.0%)

 Yes

531 (15.6%)

20 (19.6%)

3 (10.0%)

14 (22.6%)

3 (30.0%)

  1. Family history of hematologic malignancy is self report.
  2. Personal history of prior solid tumor cancer is self report.