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. 2019 Jul 24;9:667. doi: 10.3389/fonc.2019.00667

Table 3.

Concordance in risk stratification between the BCT score and Oncotype DX RS in patients aged ≤50 years according to clinical risk.

All
(n = 514)
Lymph node-negative
(n = 410)
Lymph node-positive
(n = 104)
Oncotype DX RS
(TAILORx cut-off according to clinical risk)
Oncotype DX RS
(TAILORx cut-off according to clinical risk)
Oncotype DX RS
(TAILORx cut-off according to clinical risk)
n (%) Non-chemobenefit
(0–15 for clinical high risk or 0–20 for clinical low risk)
Chemobenefit
(≥21 for clinical low risk or ≥16 for clinical high risk)
Total Non-chemobenefit
(0–15 for clinical high risk or 0–20 for clinical low risk)
Chemobenefit
(≥21 for clinical low risk or ≥16 for clinical high risk)
Total Non-chemobenefit
(0–15 for clinical high risk or 0–20 for clinical low risk)
Chemobenefit
(≥21 for clinical low risk or ≥16 for clinical high risk)
Total
BCT score Low risk (<4) 245 (47.7%) 105 (20.4%) 350 (68.1%) 217 (52.9%) 82 (20.0%) 299 (72.9%) 28 (26.9%) 23 (22.1%) 51 (49.0%)
High risk (≥4) 68 (13.2%) 96 (18.7%) 164 (31.9%) 44 (10.7%) 67 (16.3%) 111 (27.1%) 24 (23.1%) 29 (27.9%) 53 (51.0%)
Total 313 (60.9%) 201 (39.1%) 514 (100.0%) 261 (63.7%) 149 (36.3%) 410 (100.0%) 52 (50.0%) 52 (50.0%) 104 (100.0%)

BCT, Breast Cancer Test; RS, recurrence score; TAILORx, Trial Assigning Individualized Options for Treatment.

Clinical risk was determined using the modified Adjuvant! Online as reported in the MINDACT trial.