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. 2016 Jun 3;11(6):e0156789. doi: 10.1371/journal.pone.0156789

Table 6. Impact of BRCA1/2 P/LP variants on the DFS of breast cancer patients from subgroups of N0 and N1~3.

P/LP variants #Cases (events) HR (95% CI) a P a Adjusted HR (95% CI) b P b
N0
Germline and somatic combined variants
Non-carrier 165 (9) 1 1
BRCA1 11 (2) 4.08 (0.86–19.4) 0.08 1.7 (0.28–10.32) 0.56
BRCA2 12 (0) 0 0.98 0 0.99
Germline variants
Non-carrier 165 (9) 1 1
BRCA1 9 (2) 5.4 (1.12–26.0) 0.04 3.62 (0.47–27.63) 0.21
BRCA2 10 (0) 0 0.99 0 0.99
Somatic variants
Non-carrier 165 (9) 1 1
BRCA1/2 4 (0) 0 0.70 0 0.99
N1~N3
Germline and somatic combined variants
Non-carrier 215 (26) 1 1
BRCA1 8 (1) 1.01 (0.14–7.47) 0.99 0.7 (0.08–6.02) 0.74
BRCA2 15 (0) 0 0.98 0 0.98

a Univariate Cox proportional hazards regression models

b Multivariate Cox proportional hazards regression models. HR was adjusted by age at diagnosis, molecular subtype (Luminal A, Luminal B, TNBC, HER2+ and ER-PR+), tumor grade (grade I/II and III) and administration of standard therapy.