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. 2017 Apr 18;116(10):1329–1339. doi: 10.1038/bjc.2017.97

Table 4. A subgroup analysis was completed based on ER/PR+ and triple-negative tumours.

Subgroup Best feature Model %Sn %Sp AUC
ER/PR+ Hb-con Logistic regression 76.2 66.7 0.746
  HbO2-hom Naive Bayes 93.3 90.1 0.883
  HbO2-con k-NN 85.8 82.5 0.851
Triple negative Hb-hom Logistic regression 100.0 33.3 0.917
  Hb-ene Naive Bayes 100.0 66.7 0.667
  Hb-hom k-NN 75.0 66.7 0.917
FEC-D TOI-hom Logistic regression 100.0 92.3 0.949
  Hb-con Naive Bayes 60.0 81.7 0.722
  Hb-hom k-NN 80.0 80.0 0.806
AC-T HbO2-cor Logistic regression 100.0 71.4 0.837
  HbO2-hom Naive Bayes 96.4 90.7 0.882
  HbO2-hom k-NN 83.6 85.0 0.896

Abbreviations: AC-T=adriamycin, cyclophosphamide, taxol; AUC=area under curve; ER=oestrogen receptor; FEC-D=fluorouracil, epirubicin, cyclophosphamide, docetaxel; Hb=deoxy-haemoglobin; HbO2=oxy-haemoglobin; k-NN=k-nearest neighbour; PR=progesterone receptor; Sn=sensitivity; Sp=specificity; TOI=tissue optical index.

Patients were also grouped according to chemotherapy type for analysis. Three classification models were used (logistic regression, naive Bayes, and k-NN) and the best predictive features are presented.