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. 2019 Sep 9;12(12):1557–1565. doi: 10.1016/j.tranon.2019.08.008

Table 4.

Comparison of molecular subtyping using MP and BP tests (Luminal A for Low Risk MP and Luminal B for High Risk) between NGS Beta Site and IHC according to Prat et al. (n = 124) (A), between NGS Beta Site and IHC according to Maisonneuve et al. (n = 124) (B), between NGS Beta Site and microarray Agendia (n = 124) (C), and between NGS Beta Site and NGS Agendia (n = 114) (D). These results show a concordance of 71.8% (89/124) (A), 76.6% (95/124) (B), 89.5% (111/124) (C) and 93.9% (107/114) (D).

A.


MP/BP NGS Beta Site
IHC Luminal A Luminal B HER2 Basal Total
Luminal A-like 52 18 0 0 70
Luminal B-like,
HER2-negative
10 11 0 1 22
Luminal B-like,
HER2-positive
5 7 5 0 17
HER2-positive 0 0 3 0 3
Triple negative 0 1 0 11 12
Total 67 37 8 12 124
B.
Luminal A-like 53 13 0 0 66
Luminal A-like 53 13 0 0 66
Luminal B-like,
HER2-negative
9 16 0 1 26
Luminal B-like,
HER2-positive
5 7 5 0 17
HER2-positive 0 0 3 0 3
Triple negative 0 1 0 11 12
Total 67 37 8 12 124
C.
Microarray Luminal A Luminal B HER2 Basal Total
Luminal A 60 4 0 0 64
Luminal B 7 31 0 0 38
HER2 0 2 8 0 10
Basal 0 0 0 12 12
Total 67 37 8 12 124
D.
NGS Agendia Luminal A Luminal B HER2 Basal Total
Luminal A 58 1 0 0 59
Luminal B 6 31 0 0 37
HER2 0 0 7 0 7
Basal 0 0 0 11 11
Total 64 32 7 11 114

For 10 samples, no NGS results were obtained at Agendia.