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. 2020 Jul 8;23(3-4):100–109. doi: 10.1159/000508684

Table 3.

Time of registration and first meeting at the Oncogenetic Clinic in Lund and genetic testing of the BC patients

Registered (n = 179) First meeting (n = 165) Genetic testing
alla(n = 167) no pathogenic variantsa, b(n = 134) BRCA1 (n = 19) BRCA2 (n = 9) other pathogenic variantsc(n = 5)
Before BC diagnosis
 <–15 years 11 (6.1) 6 (3.6) 4 (2.4) 0 3 (15.8) 1 (11.1) 0
After BC diagnosis
 0–1 years 73 (40.8) 73 (44.2) 53 (31.7) 42 (31.3) 6 (31.6) 4 (44.4) 1 (20.0)
 1–2 years 39 (21.8) 42 (25.5) 52 (31.1) 46 (34.3) 3 (15.8) 2 (22.2) 1 (20.0)
 2–3 years 12 (6.7) 12 (7.3) 18 (10.8) 16 (11.9) 1 (5.3) 1 (11.1) 0
 3–4 years 7 (3.9) 6 (3.6) 10 (6.0) 6 (4.5) 2 (10.5) 0 2 (40.0)
 4–5 years 5 (2.8) 4 (2.4) 4 (2.4) 3 (2.2) 1 (5.3) 0 0
 5–10 years 21 (11.7) 16 (9.7) 18 (10.8) 15 (11.2) 1 (5.3) 1 (11.1) 1 (20.0)
 10–15 years 11 (6.1) 6 (3.6) 7 (4.2) 6 (4.5) 1 (5.3) 0 0
Missing 0 0 1 (0.6) 0 1 (5.3) 0 0

Data are presented as n (%).

a

Of which 2 BC patients underwent genetic testing without being registered at the Oncogenetic Clinic in Lund.

b

Genetic testing without findings, including variants of uncertain significance.

c

Positive for a germline pathogenic variant in TP53 (n = 3) or CHEK2 (n = 2).