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

Table 3. Regression coefficients (r) of the multiple regression analysis for DOS–GLCM features and corresponding regression.

DOS–GLCM feature Comparison r F-value P-value
Hb-homogeneity Age −0.130 0.599 0.444
  ER/PR status −0.087 0.267 0.608
  Her2 status −0.104 0.382 0.540
  Tumour size +0.231 1.967 0.170
  Miller–Payne grade −0.358 5.137 0.030
HbO2-correlation Age −0.116 0.475 0.495
  ER/PR status −0.003 0.000 0.988
  Her2 status −0.109 0.418 0.522
  Tumour size −0.295 3.335 0.076
  Miller–Payne grade +0.375 5.172 0.022
HbT-homogeneity Age −0.142 0.715 0.403
  ER/PR status +0.007 0.002 0.969
  Her2 status +0.206 1.544 0.222
  Tumour size +0.085 0.257 0.616
  Miller–Payne grade −0.233 2.015 0.165
St-contrast Age −0.231 1.972 0.169
  ER/PR status +0.056 0.111 0.741
  Her2 status +0.095 0.322 0.574
  Tumour size −0.164 0.971 0.331
  Miller–Payne grade +0.177 1.138 0.293
StO2-contrast Age −0.083 0.241 0.626
  ER/PR status −0.074 0.190 0.665
  Her2 status −0.213 1.661 0.206
  Tumour size +0.279 2.966 0.094
  Miller–Payne grade 0.325 4.140 0.050

Abbreviations: DOS=diffuse optical spectroscopy; ER=oestrogen receptor; GLCM=grey-level co-occurrence matrices; Hb=deoxy-haemoglobin; HbO2=oxy-haemoglobin; HbT=total haemoglobin; PR=progesterone receptor; StO2=tumour oxygen saturation; St=oxygen desaturation.

F-values are presented. Clinical features such as age, ER/PR status, Her2 status, and tumour size were not significantly correlated to DOS–GLCM features in this patient cohort. However, DOS–GLCM features such as the Hb-hom, HbO2-cor, StO2-con were correlated to Miller–Payne pathologic response grade. Statistically significant values are in bold.