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. 2014 Aug 9;106(8):dju165. doi: 10.1093/jnci/dju165

Table 1.

Immunohistochemical staining for the intrinsic breast cancer molecular subtypes*

IHC subtype (%)† ER and/or PR HER2 Ki67 Intrinsic subtype
Luminal A (73%) Positive Negative Low Luminal A
Luminal B (10%) Positive Negative
or positive
Low or high Luminal B
HER2 positive, nonluminal (5%) Negative Positive Not needed HER2-enriched
Triple-negative (12%) Negative Negative Not needed Basal-like

* There are two predominantly hormone-positive (estrogen receptor [ER] and/or progesterone receptor [PR]) intrinsic molecular subtypes (luminal A and luminal B) and two predominantly hormone-negative intrinsic subtypes (human epidermal growth factor receptor 2 [HER2] enriched and basal-like) (133–136). Additionally, there are two predominantly HER2-positive intrinsic molecular subtypes (luminal B and HER2 enriched) and two predominantly HER2-negative intrinsic subtypes (luminal A and Basal-like). Adapted from Goldhirsch et al. (157). IHC = immunohistochemical.

† Estimated percentage distribution for IHC-derived subtypes among women with breast cancer and known ER, PR, and HER2 expression in the general population of the United States in 2010, provided by the National Cancer Institute’s SEER database (178).