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. 2022 May 9;8:61. doi: 10.1038/s41523-022-00423-z

Table 4.

Cox regression models for BCFi and OS by luminal PAM50 subtypes, tamoxifen treatment, and PAM50 subtype by treatment interaction in patients with ER-positive/HER2-negative tumours.

BCFi OS
HR (95% CI); P-value
0–10 years
(n = 217, n = 92 events) (n = 217, n = 64 events)
TAM vs control in LumAPAM50 0.41 (0.23–0.74); 0.003 0.61 (0.30–1.26); 0.18
TAM vs control in LumBPAM50 1.19 (0.63–2.27); 0.59 1.76 (0.85–3.63); 0.13
Interaction luminal PAM50 subtype x TAM 0.34 (0.14–0.83); 0.02 0.35 (0.13–0.97); 0.04
>10 yearsa
(n = 121, n = 43 events) (n = 153, n = 74 events)
TAM vs control in LumAPAM50 0.69 (0.35–1.37); 0.29 0.74 (0.44–1.25); 0.26
TAM vs control in LumBPAM50 0.17 (0.04–0.80); 0.03 0.25 (0.08–0.77); 0.02
Interaction luminal PAM50 subtype x TAM 4.05 (0.74–22.1); 0.11 2.95 (0.85–10.2); 0.09
Maximum follow-up timeb
(n = 217, n = 135 events) (n = 217, n = 138 events)
TAM vs control in LumAPAM50 0.52 (0.34–0.81); 0.004 0.71 (0.46–1.08); 0.11
TAM vs control in LumBPAM50 0.80 (0.45–1.41); 0.44 0.87 (0.49–1.54); 0.63
Interaction luminal PAM50 subtype x TAM 0.65 (0.32–1.34); 0.24 0.82 (0.40–1.65); 0.57

All analyses are stratified by study region.

BCFi, breast cancer-free interval; CI, confidence interval; ER, oestrogen receptor; HER2, human epidermal growth factor receptor 2; HR, hazard ratio; Lum, Luminal; OS, overall survival; TAM, tamoxifen.

aFrom year 10 to maximum follow-up time.

b32 and 36 years regarding BCFi and OS, respectively.