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. 2020 Jul 27;11:3747. doi: 10.1038/s41467-020-17537-2

Table 1.

Clinicopathological characteristics of SCAN-B TNBC patients.

BRCA1 hypermethylated BRCA1-nulla non-BRCA1
N 57 25 155
Age
     <35 years 14.0% 28.0% 0.6%
     35–50 years 28.1% 12.0% 11.0%
     50–70 years 47.4% 52.0% 43.9%
     ≥70 years 10.5% 8.0% 44.5%
Germline BRCA1 variantb 0% 76% 0%
Tumor size
     ≤20 mm 57.9% 52.0% 47.7%
     >20 mm 42.1% 48.0% 52.3%
Nodal status
     Node negative 70.2% 48.0% 65.2%
     Node positive 28.1% 48.0% 34.2%
     Missing data 1.8% 4.0% 0.6%
Tumor grade
     Grade 2 0% 0% 18.1%
     Grade 3 98.2% 96.0% 80.0%
     Missing data 1.8% 4.0% 1.9%
ER-staining positivityc
     <1% 89.5% 84.0% 87.6%
     1–10% 10.5% 16.0% 12.4%
Therapyd
     Chemotherapy 87.5% 91.7% 66.9%
     Untreated 12.5% 8.3% 33.1%
 IDFS evente 17.5% 28.0% 38.7%
 Median IDFS for patients (years)f 5.0 (0.1–7.1) 4.8 (0.2–6.7) 4.6 (0.6–7.2)
 DRFI evente 10.5% 20.0% 24.5%
 Median DRFI for patients (years)f 4.6 (0.1–7) 4.1 (0.05–6.6) 4.3 (0.4–7.2)
 Death eventE 14.0% 24.0% 31.6%
 Median OS for patients (years)f 4.7 (0.2–7.1) 4.1 (2.9–6.8) 4.6 (2.7–7.1)

Data obtained from the Swedish national breast cancer quality registry. Cases with missing data omitted from calculations if not shown as separate variable.

aBRCA1-null includes cases with both germline and somatic BRCA1 inactivating genetic variants.

bBased on whole genome sequencing data.

cIn Sweden, ER-negativity is defined as ≤10% of cells with IHC-staining for ER.

dIncludes all cases irrespective if eligible for outcome analysis, but excluding cases with palliative treatment.

eIncludes all events, irrespective of eligibility for outcome analysis.

fTime and range for patients without an event, irrespective of eligibility for outcome analysis.