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. 2017 Nov 28;8(68):112258–112267. doi: 10.18632/oncotarget.22733

Table 3. Correlation between patient characteristics and pathogenic germline variants in BRCA1/2 or any tested genes among 230 patients with OCa.

Clinicopathological features n Pathogenic BRCA1/2 mutation P valueb Pathogenic mutations in any tested gene P valueb
Positive Negative Positive Negative
Age
 <55 117 20 97 0.0132 28 89 0.0159
 ≥55 113 7 106 13 100
Histologic subtypec
 HGSC 74 22 52 <0.0001 30 44 <0.0001
 Non-HGSC 156 5 151 11 145
Stage
 I 107 11 96 0.5460 21 86 0.6050
 II - IV 123 16 107 20 103
Personal history of breast cancera
 Diagnosed with breast cancer 6 2 4 0.1480 3 3 0.0714
 Not diagnosed with breast cancer 224 25 199 38 186
One or more family members with breast cancera,d
 Present 26 5 21 0.3260 6 20 0.4040
 Absent 154 17 137 25 129
One or more family members with ovarian cancera,d
 Present 13 6 7 0.0017 7 6 0.0019
 Absent 167 16 151 24 143
One or more family members with ovarian or breast cancera,c
 Present 32 7 25 0.0775 9 23 0.1180
 Absent 148 15 133 22 126

aAmong 230 patients, a detailed family history was available for 180 patients.

bFisher's exact test.

cHGSC, high-grade serous carcinoma.

dFamily history of cancer, including first- or second-degree relatives.