Table 2.
Description of main patient and clinical factors used for evaluation of the models and formula
Studya/geographic area | Europe —otherb | Europe—Scandinavia | Europe—United Kingdom | Netherlands— BOSOM | Netherlands— EMC | Netherlands— NCR | United States and Australia |
---|---|---|---|---|---|---|---|
N | 15,183 | 12,928 | 11,921 | 3760 | 3390 | 83,138 | 2436 |
Age at first diagnosis, years (%) | |||||||
< 30 | 152 (1.0) | 46 (0.4) | 156 (1.3) | 108 (2.9) | 46 (1.4) | 388 (0.5) | 41 (1.7) |
30–39 | 1252 (8.2) | 489 (3.8) | 1811 (15.2) | 842 (22.4) | 374 (11.0) | 4241 (5.1) | 494 (20.3) |
40 + | 13,779 (90.8) | 12,393 (95.9) | 9954 (83.5) | 2810 (74.7) | 2970 (87.6) | 78,509 (94.4) | 1901 (78.0) |
Age at first birth = unknown (%) | 15,183 (100.0) | 12,928 (100.0) | 11,921 (100.0) | 3760 (100.0) | 3390 (100.0) | 83,138 (100.0) | 2436 (100.0) |
Family history (%) | |||||||
Yes | 2123 (14.0) | 818 (6.3) | 1371 (11.5) | 737 (19.6) | 591 (17.4) | 0 (0.0) | 319 (13.1) |
No | 8057 (53.1) | 3158 (24.4) | 8210 (68.9) | 1177 (31.3) | 2482 (73.2) | 0 (0.0) | 1498 (61.5) |
Unknown | 5003 (33.0) | 8952 (69.2) | 2340 (19.6) | 1846 (49.1) | 317 (9.4) | 83,138 (100.0) | 619 (25.4) |
First BC type = Pure invasive (%) | 15,183 (100.0) | 12,928 (100.0) | 11,921 (100.0) | 3760 (100.0) | 3390 (100.0) | 83,138 (100.0) | 2436 (100.0) |
Breast density = unknown (%) | 15,183 (100.0) | 12,928 (100.0) | 11,921 (100.0) | 3760 (100.0) | 3390 (100.0) | 83,138 (100.0) | 2436 (100.0) |
ER status (%) | |||||||
Negative | 3387 (22.3) | 1746 (13.5) | 1718 (14.4) | 896 (23.8) | 842 (24.8) | 14,591 (17.6) | 445 (18.3) |
Positive | 10,071 (66.3) | 9401 (72.7) | 7175 (60.2) | 2024 (53.8) | 2427 (71.6) | 64,790 (77.9) | 1572 (64.5) |
Unknown | 1725 (11.4) | 1781 (13.8) | 3028 (25.4) | 840 (22.3) | 121 (3.6) | 3757 (4.5) | 419 (17.2) |
High-risk pre-neoplasia = unknow n (%) | 15,183 (100.0) | 12,928 (100.0) | 11,921 (100.0) | 3760 (100.0) | 3390 (100.0) | 83,138 (100.0) | 2436 (100.0) |
Anti-estrogen therapy (%) | |||||||
Yes | 7868 (51.8) | 6434 (49.8) | 8712 (73.1) | 809 (21.5) | 1559 (46.0) | 40,214 (48.4) | 363 (14.9) |
No | 4570 (30.1) | 1947 (15.1) | 2046 (17.2) | 2739 (72.8) | 1821 (53.7) | 42,924 (51.6) | 8 (0.3) |
Unknown | 2745 (18.1) | 4547 (35.2) | 1163 (9.8) | 212 (5.6) | 10 (0.3) | 0 (0.0) | 2065 (84.8) |
CBC cumulative incidence (%) | |||||||
3-year (95% CI) | 1.0 (0.8–1.2) | 0.7 (0.5–0.9) | 0.5 (0.3–0.7) | 1.7 (1.3–2.1) | 1.7 (1.2–2.1) | 1.3 (1.2–1.4) | 1.8 (0.8–2.8) |
5-year (95% CI) | 1.6 (1.4–1.9) | 1.0 (0.8–1.3) | 1.0 (0.8–1.3) | 3.0 (2.5–3.6) | 2.6 (2.1–3.2) | 2.4 (2.3–2.5) | 2.8 (1.7–3.8) |
10-year (95% CI) | 3.5 (3.1–3.9) | 2.1 (1.7–2.4) | 1.3 (1.0–1.5) | 5.5 (4.7–6.2) | 5.7 (4.9–6.6) | 4.6 (4.5–4.8) | 4.1 (3.0–5.3) |
More details about the main patient and clinical characteristics by study are available in the supplementary information of [5]
BOSOM Breast Cancer Outcome Study of Mutation carriers, EMC Erasmus Medical Center, NCR Netherlands Cancer Registry, BC breast cancer, ER estrogen receptor, CBC contralateral breast cancer, CI confidence interval
The studies denoted with Europe and United States and Australia are part of the Breast Cancer Association Consortium
Europe—other geographic area included studies from Belgium (1), Germany (2), Netherlands (2) and Poland (2)