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Table 5 Correlation between PIK3CA mutation status and response to neoadjuvant FAC/FEC or TFAC/TFEC chemotherapies

From: PIK3CA-activating mutations and chemotherapy sensitivity in stage II–III breast cancer

  

FAC/FECa chemotherapy

TFAC/TFECa chemotherapy

  

PIK3CA wild-type (n = 51)

PIK3CA mutation (n = 12)

P valueb

PIK3CA wild-type (n = 66)

PIK3CA mutation (n = 11)

P valueb

Pathological complete response (pCR) versus residual disease (RD)

RD

48 (94%)

11 (92%)

1.000

47 (73%)

7 (70%)

1.000

 

pCR

3 (6%)

1 (8%)

 

17 (27%)

3 (30%)

 
 

Unknown

-

-

-

2

1

-

Residual cancer burden

0

6 (17.6%)

1 (16.7%)

0.334 (0.474c)

14 (24.6%)

3 (33.3%)

0.438 (0.613c)

 

I

2 (5.9%)

0 (0%)

 

5 (8.8%)

0 (0%)

 
 

II

16 (47.1%)

5 (83.3%)

 

21 (36.8%)

5 (55.6%)

 
 

III

10 (29.4%)

0 (0%)

 

17 (29.8%)

1 (11.1%)

 
 

Unknown

17

6

-

9

2

-

  1. aFor description, please refer to text. bChi-square test. c P value for comparison of residual cancer burden (RCB)-0 and RCB-I versus RCB-III. FAC, 5-fluoruracil, doxorubicin, and cyclophosphamide; FEC, 5-fluoruracil, epirubicin, and cyclophosphamide; PIK3CA, phosphatidylinositol 3-kinase, catalytic, alpha polypeptide; TFAC, paclitaxel followed by 5-fluoruracil, doxorubicin, and cyclophosphamide; TFEC, paclitaxel followed by 5-fluoruracil, epirubicin, and cyclophosphamide.