Tumor description
|
|
Metachronous |
93 (66.9%) |
Synchronous |
46 (33.1%) |
Sex
|
|
Female
|
137 |
Male
|
2 |
Age at diagnosis (years)
|
|
Primary tumor
|
|
Median (range)
|
45 (21–77) |
≤40 |
41 (29.5%) |
41–50 |
53 (38.12%) |
51–60 |
29 (20.9%) |
≥60 |
16 (11.5%) |
Secondary tumor
|
|
Median (range)
|
51 (21–80) |
≤40 |
21 (15.1%) |
41–50 |
48 (34.5%) |
51–60 |
40 (28.8%) |
≥60 |
30 (21.6%) |
Time between 1st and 2nd tumors (years)
|
|
Median ± DS
|
4 ± 6.08 |
≤5 |
88 (63.3%) |
6–10 |
27 (19.4%) |
>10 |
24 (17.3%) |
Histology 1st breast cancer
|
|
Ductal in situ |
96 (69%) |
Ductal invasive |
13 (9.4%) |
Lobular invasive |
12 (8.6%) |
Others |
18 (13%) |
Histology 2nd breast cancer
|
|
Ductal in situ |
16 (11.5%) |
Ductal invasive |
92 (66.2%) |
Lobular invasive |
15 (10.8%) |
Others |
16 (11.5%) |
Molecular phenotype 1st breast cancer
|
|
Luminal A |
28 (20.1%) |
Luminal B/HER2 - |
49 (35.3%) |
Luminal B/HER2 + |
7 (5%) |
HER2 + (non-luminal) |
6 (4.3%) |
Triple negative |
12 (8.6%) |
Unknown |
37 (26.7%) |
Molecular phenotype 2nd breast cancer
|
|
Luminal A |
35 (25.2%) |
Luminal B/HER2 - |
35 (25.2%) |
Luminal B/HER2 + |
10 (7.2%) |
HER2 + (non-luminal) |
5 (3.6%) |
Triple negative |
17 (12.2%) |
Unknown |
37 (26.6%) |
Genetic testing results
|
|
Pathogenic variant BRCA1
|
13 (9.3%) |
Pathogenic variant BRCA2
|
19 (13.7%) |
Pathogenic variant BRCA1/BRCA2
|
1 (0.7%) |
Pathogenic variant CHEK2
|
5 (3.6%) |
Pathogenic variant PALB2
|
8 (5.8 %) |
Pathogenic variant ATM
|
3 (2.2%) |
Pathogenic variant PTEN
|
1 (0.7%) |
Pathogenic variant RAD51C
|
2 (1.4%) |
Pathogenic variant MUTHY
|
1 (0.7%) |
Variant of uncertain significance |
27 (19.4%) |
Negative |
59 (42.5%) |
Type of surgery 1st breast cancer
|
|
Mastectomy |
50 (36.2%) |
Breast conserving therapy |
74 (53.2%) |
Unknown |
15 (10.9%) |
Type of surgery 2nd breast cancer
|
|
Mastectomy |
48 (34.5%) |
Breast conserving therapy |
55 (39.9%) |
Unknown |
35 (25.3%) |