Table 1: Patients with ovarian carcinoma, extra-ovarian peritoneal carcinoma and fallopian tube carcinoma with BRCA1/2 study.
Patient |
Primary tumor |
Tumor BRCA 1/2 |
GCU visit |
Germline BRCA 1/2 |
1 |
Ovarian |
NPV |
No |
NS |
2 |
Ovarian |
NPV |
Yes |
NPV |
3 |
Ovarian |
NPV |
Yes |
NPV |
4 |
Synchronous ovarian and endometrial cancer |
NPV |
No |
NS |
5 |
Ovarian |
NPV |
Yes |
NPV |
6 |
Ovarian |
NPV |
Yes |
NPV |
7 |
Ovarian |
BRCA1 mutation |
Yes |
Normal |
8 |
Ovarian |
BRCA1 mutation |
Yes |
BRCA1 mutation |
9 |
Ovarian |
NPV |
Yes |
NPV |
10 |
Ovarian |
NPV |
Yes |
NS |
11 |
Ovarian |
NPV |
No |
NS |
12 |
Ovarian |
BRCA1 mutation |
Yes |
Normal |
13 |
Ovarian |
NPV |
No |
NS |
14 |
Ovarian |
BRCA1 mutation |
Yes |
BRCA1 mutation |
15 |
Ovarian |
BRCA2 mutation |
Yes |
BRCA2 mutation |
16 |
Ovarian |
NPV |
Yes |
NS |
17 |
Ovarian |
NPV |
Yes |
NS |
18 |
Ovarian |
BRCA1 mutation |
Yes |
BRCA1 mutation |
19 |
Ovarian |
NPV |
Yes |
NPV |
20 |
Ovarian |
NPV |
No |
NS |
21 |
Ovarian |
NPV |
Yes |
NPV |
22 |
Ovarian |
Insufficient sample |
Yes |
NPV |
23 |
Ovarian |
NPV |
Yes |
NS |
24 |
Ovarian |
NPV |
Yes |
NPV |
25 |
Peritoneal extraovarian carcinoma |
NPV |
No |
NS |
26 |
Ovarian |
NPV (BRCA2 VUS) |
Yes |
NPV |
27 |
Ovarian |
NPV |
Yes |
NPV |
28 |
Ovarian |
NPV |
Yes |
NS |
29 |
Ovarian |
Insufficient sample |
Yes |
BRCA1 mutation |
30 |
Ovarian |
NPV |
No |
NS |
31 |
Peritoneal extraovarian carcinoma |
NPV |
Yes |
NPV |
32 |
Ovarian/peritoneal extraovarian carcinoma |
NPV |
No |
NS |
33 |
Ovarian |
NPV |
No |
NS |
34 |
Ovarian |
NPV |
Yes |
NPV |
35 |
Ovarian |
NPV |
Yes |
NPV (BRCA1 VUS) |
36 |
Ovarian |
NPV |
Yes |
NPV |
37 |
Ovarian |
Insufficient sample |
Yes |
BRCA2 mutation |
38 |
Ovarian |
BRCA1 mutation |
Yes |
Normal |
39 |
Ovarian |
BRCA1 mutation |
Yes |
BRCA1 mutation |
40 |
Ovarian |
BRCA1 mutation |
Yes |
BRCA1 mutation |
41 |
Ovarian |
Insufficient sample |
No |
NS |
42 |
Fallopian tube |
BRCA2 mutation |
Yes |
BRCA2 mutation |
43 |
Ovarian |
NPV |
No |
NS |
NPV: no pathogenic variants (when both genes are studied); Normal: no mutation (when only the pathogenic variant uncovered at the tumor is studied); NS: not studied; VUS: variant of unknown significance.