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Table 3 Correlation between PIK3CA mutation status and clinical variables

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

  

PIK3CA wild-type

PIK3CA mutated

P valuea

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

RD

95 (83%)

18 (82%)

1.000

 

pCR

20 (17%)

4 (18%)

 
 

Unknown

2

1

-

Residual cancer burden

0

20 (22.0%)

4 (26.7%)

0.121 (0.166b)

 

I

7 (7.7%)

0 (0%)

 
 

II

37 (40.7%)

10 (66.7%)

 
 

III

27 (29.7%)

1 (6.7%)

 
 

Unknown

26

8

-

Estrogen receptor (ER) status

ER-

54 (46%)

8 (35%)

0.365

 

ER+

63 (54%)

15 (65%)

 

Progesterone receptor (PR) status

PR-

71 (60.7%)

11 (47,8%)

0.259

 

PR+

46 (39.3)

12 (52,2%)

 

HER2 status

HER2-

104 (89%)

21 (91%)

1.000

 

HER2+

13 (11%)

2 (9%)

 

Grade

Grade 1–2

46 (47%)

10 (56%)

0.612

 

Grade 3

51 (53%)

8 (44%)

 
 

Unknown

20

5

-

Nodal status

Negative

29 (25%)

12 (52%)

0.012

 

Positive

88 (75%)

11 (48%)

 

Tumor size

T0

1 (1%)

1 (4%)

0.535

 

T1

7 (6%)

0 (0%)

 
 

T2

59 (50%)

12 (52%)

 
 

T3

18 (15%)

3 (13%)

 
 

T4

32 (27%)

7 (30%)

 

Ethnicity

Asian

2 (2%)

1 (4%)

0.505

 

Black

11 (9%)

2 (9%)

 
 

Hispanic

40 (34%)

10 (43%)

 
 

Caucasian

64 (55%)

10 (43%)

 

Median age (minimum-maximum), years

 

50 (28–73)

52 (42–73)

-

  1. aChi-square test. b P value for comparison of residual cancer burden (RCB)-0 and RCB-I versus RCB-III. PIK3CA, phosphatidylinositol 3-kinase, catalytic, alpha polypeptide.