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Table 1 Clinical and pathological data in the study

From: Predicting the response to neoadjuvant chemotherapy for breast cancer: wavelet transforming radiomics in MRI

 

pCR

Non-pCR

P-value

No. of patients

17

38

N/A

Age(y)

 Median(range)

50 (37–70)

48 (25–68)

N/A

 Mean ± SD

50.7 ± 9.4

49.5 ± 10.4

0.676

Enhancement Type, No. (%)

  

0.506

 Masslike

11 (64.7)

23 (60.5)

 

 Non-masslike

6 (35.3)

15 (39.5)

 

Max-D(cm)*

 Median(range)

2.6 (2.3–3.7)

4.2 (3.1–5.4)

N/A

 Mean ± SD

2.9 ± 1.1

4.3 ± 1.9

0.002

Subtype, No. (%)

  

0.493

 Luminal A

5 (29.4)

17 (44.7)

 

 Luminal B

2 (11.8)

7 (18.4)

 

 Her-2

5 (29.4)

8 (21.1)

 

 TNBC

5 (29.4)

6 (15.8)

 

Regimen, No. (%)

  

0.412

 EC + Taxol

4 (23.5)

14 (36.8)

 

 FEC + Taxol

7 (41.2)

15 (39.5)

 

 AC+ Taxol

2 (11.8)

6 (15.8)

 

 Others

4 (23.5)

3 (7.9)

 
  1. NOTE. P-values were calculated by T-test or Mann-Whitney U test for Age, Max-D, from Chi-square test or Fisher’s exact test for Enhancement type, Subtype, Regimen
  2. Abbreviations: Max-D Maximum- diameter, Her-2 Human epidermal growth factor receptor 2, TNBC Triple negative breast cancer, E epirubicin; C cyclophosphamide, Taxol paclitaxel; F 5-fluoroucil. A doxorubicin. N/A Not available