Skip to main content

Table 1 Patient and treatment characteristics

From: Hsa-miR-375 is a predictor of local control in early stage breast cancer

Patient and treatment characteristics

       

Parameters

Pilot phase n = 32

Validation phase n = 115

Relapse n = 16

Control n = 16

p value

Relapse n = 30

Control n = 85

p value

Age at diagnosis (years)

Median

53.5

52

0.88

52

54

0.59

Range

36–71

35–74

33–79

37–78

Menopause (n)

No

4 (25 %)

4 (25 %)

1.0

11 (36.7 %)

32 (37.6 %)

0.37

Yes

8 (50 %)

8 (50 %)

17 (56.7 %)

40 (47.1 %)

Unclear

4 (25 %)

4 (25 %)

2 (6.7 %)

13 (15.3 %)

T (n)

T1

10 (62.5 %)

10 (62.5 %)

1.0

26 (86.7 %)

75 (88.2 %)

0.82

T2

6 (37.5 %)

6 (37.5 %)

4 (13.3 %)

10 (11.8 %)

N (n)

N0

13 (81.3 %)

13 (81.3 %)

1.0

24 (80 %)

67 (78.8 %)

0.88

N1

2 (12.5 %)

2 (12.5 %)

6 (20 %)

18 (21.1 %)

N2

1 (6.3 %)

1 (6.3 %)

0

0

M (n)

M0

16 (100 %)

16 (100 %)

1.0

30 (100 %)

85 (100 %)

1.0

M1

0

0

0

0

Grading (n)

G1

1 (6.3 %)

0

0.87

3 (10 %)

8 (9.4 %)

0.75

G2

8 (50 %)

9 (56.3 %)

18 (60 %)

55 (64.7 %)

G3

7 (43.8 %)

7 (43.8 %)

9 (30 %)

22 (25.9 %)

Histology (n)

IDC

13 (81.3 %)

15 (93.8 %)

0.56

22 (73.3 %)

63 (74.1 %)

0.98

ILC

3 (18.8 %)

1 (6.3 %)

5 (16.7 %)

12 (14.1 %)

Tubular

0

0

2 (6.7 %)

6 (7.1 %)

Other

0

0

1 (3.3 %)

4 (4.7 %)

In situ component (n)

Yes

14 (87.5 %)

10 (62.5 %)

0.24

17 (56.7 %)

47 (55.3 %)

0.97

No

2 (12.5 %)

6 (6.25 %)

13 (43.3 %)

35 (41.2 %)

Lymphangiosis

0

0

0

1 (1.2 %)

Not stated

0

0

0

2 (2.4 %)

Receptors (n)

ER positive

8 (50 %)

10 (62.5 %)

0.56

23 (76 %)

67 (78.8 %)

0.81

ER negative

8 (50 %)

6 (37.5 %)

7 (23.3 %)

18 (21.2 %)

PR positive

8 (50 %)

8 (50 %)

0.56

19 (63.3 %)

62 (72.9 %)

0.32

PR negative

8 (50 %)

8 (50 %)

11 (36.7 %)

23 (27.1 %)

her2neu

Positive

8 (50 %)

4 (25 %)

0.24

11 (37 %)

24 (28 %)

0.81

Negative

5 (31 %)

9 (56 %)

18 (60 %)

44 (52 %)

Not assessable

3 (19 %)

3 (19 %)

1 (3 %)

17 (20 %)

Proliferation index

ki67 < 20 %

10 (63 %)

6 (38 %)

0.24

15 (50 %)

49 (58 %)

0.78

ki67 > 20 %

5 (31 %)

9 (56 %)

10 (33 %)

26 (31 %)

Not assessable

1 (6 %)

1 (6 %)

5 (17 %)

10 (11 %)

Boost (n)

Intraoperative

8 (50 %)

8 (50 %)

1.0

11 (36.7 %)

34 (40 %)

0.91

Percutaneous

8 (50 %)

8 (50 %)

16 (53.3 %)

51 (60 %)

None

0

0

3 (10 %)

0

Boost dose (Gy)

Dose intraoperative

10 Gy

10 Gy

0.84

10 Gy

10 Gy

0.58

Dose percutaneous

12 Gy

12 Gy

12 (15–19) Gy

12 (9–19) Gy

WBRT dose (Gy)

Median

54 Gy

54 Gy

0.78

54 Gy

54 Gy

0.68

Range

51.2–61.2 Gy

51.2–57.8 Gy

51–63 Gy

51–57.6 Gy

Surgery (n)

BCT

16 (100 %)

15 (93.8 %)

0.78

30 (100 %)

85 (100 %)

1.0

Mastectomy

0

1 (6.3 %)

0

0

Re-Excisition (n)

Yes

8 (50 %)

4 (25 %)

0.24

12 (40 %)

33 (38.8 %)

0.91

No

8 (50 %)

12 (75 %)

18 (60 %)

52 (61.2 %)

Year of surgery (n)

Before 1998

5 (31.3 %)

5 (31.3 %)

1.0

14 (46.7 %)

38 (44.7 %)

0.85

Since 1998

11 (68.8 %)

11 (68.8 %)

16 (53.3 %)

47 (55.3 %)

Chemotherapy (n)

Yes

8 (50 %)

6 (37.5 %)

0.56

11 (36.7 %)

20 (23.5 %)

0.18

No

8 (50 %)

10 (62.5 %)

19 (63.3 %)

65 (76.5 %)

Hormonal treatment (n)

Yes

8 (50 %)

7 (43.8 %)

0.78

16 (53.3 %)

56 (65.9 %)

0.27

No

8 (50 %)

9 (56.3 %)

13 (43.3 %)

26 (30.6 %)

Unclear

0

0

1 (3.3 %)

3 (3.5 %)

Tumor burden in biopsy (%)

Median

70

50

0.34

70

50

0.52

Range

10–90

10–90

10–90

10–90

  1. Patient and treatment characteristics as well as the relative tumor burden in the samples are shown. The relapse group and control were compared with the Mann-Whitney U test. Neither in the pilot nor in the validation phase statistically significant differences of potentially prognostic parameters were detected between the relapse and the control group. The stainings for her2 and ki-67 were performed according to the standard procedures implemented at the Department of Pathology. Because some of the specimens were quite old (minimum 5 years) in some cases, the stainings—even on repetition—did not yield valid result due to technical problems with the non-adhesive FFPE sections