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. 2019 Jul 12;57(1):53–61. doi: 10.1136/jmedgenet-2019-106189

Table 2.

Association of age at primary breast cancer diagnosis, incidence of secondary cancer diagnosis and histopathology with BRCA1, BRCA2, PALB2, ATM, CHEK2, TP53 and RAD51C LoF variants

Non-carriers (n=931) BRCA1 (n=254) BRCA2 (n=81) PALB2
(n=11)
ATM
(n=18)
CHEK2 (n=25) TP53
(n=12)
RAD51C (n=7)
Mean age at first BrCa Dx Mean age±SD 41.49±10.9 38.74±9.2 40.95±9.1 41.36±10.1 42.67±8.5 42.36±8.9 30.3±6.2 43.86±7.9
P value 0.00084 0.9253 0.8932 0.3004 0.4179 0.02391 0.3432
Second BrCa Dx No 134 60 19 2 5 6 6 3
Frequency, % 14.39 23.62 23.46 18.18 27.78 24.00 50.00 42.86
P value 0.001499 0.03598 1 0.17 0.242 0.03498 0.05747
OvCa Dx No 26 45 7 0 0 0 1 1
Frequency, % 2.79 17.72 8.64 0.00 0.00 0.00 8.33 14.28
P value 0.0004998 0.01349 1 1 0.6402 0.2634 0.4253
Other Cancer Dx No 28 11 2 0 2 3 2 0
Frequency, % 3.00 4.33 2.47 0.00 11.11 12.00 16.66 0.00
P value 0.3273 1 1 0.11 0.04648 0.063 1
Non-carriers (n=931) BRCA1
(n=254)
BRCA2 (n=81) PALB2 (n=8) ATM
(n=16)
CHEK2 (n=22) TP53
(n=10)
RAD51C (n=7)
TNBC No 151 169 9 2 1 1 2 3
Frequency, % 16.22 66.54 11.11 25 6.25 4.55 20.00 42.86
P value 0.0004998 0.2509 0.6062 0.3408 0.1719 1 0.09495

All double mutation carriers have been excluded from the analysis; for PALB2, ATM, CHEK2, TP53 and RAD51C, available data from family relatives carrying LoF alleles have been included in the analysis.

Bold numbers indicate statistically significant findings.

Dx, diagnosis;LoF, loss-of-function; TNBC, triple-negative breast cancer.