Table 2 Summary of Kaplan-Meier analyses of the suitability of expression levels of six genes and pathologic features as predictors of recurrence, metastasis, and survival in patients with bladder cancer (n=251)

From: Alterations in transcription clusters underlie development of bladder cancer along papillary and nonpapillary pathways

 

Recurrence-free

Metastasis-free

Overall-survival

 

Patients (%)

P-value*

Patients(%)

P-value*

Patients (%)

P-value*

CDH1 a (low expression)

 

0.87

 

0.01

 

0.01

 Low

8

 

21

 

24

 

 High

11

 

49

 

48

 

FN1 a (high expression)

 

0.89

 

0.2

 

0.29

 Low

4

 

28

 

30

 

 High

9

 

30

 

31

 

TOP2A a (high expression)

 

0.1

 

0.01

 

0.01

 Low

9

 

45

 

48

 

 High

7

 

29

 

29

 

CDC2 a

 

0.91

 

0.3

 

0.58

 Low

7

 

35

 

36

 

 High

8

 

36

 

39

 

MMP7 a

 

0.48

 

0.99

 

0.95

 Low

0

 

25

 

27

 

 High

12

 

41

 

43

 

MMP12 a

 

0.12

 

0.25

 

0.29

 Low

18

 

42

 

45

 

 High

3

 

28

 

29

 

Cluster A vs B b

 

0.6

 

0.1

 

0.08

 Cluster A

19

 

25

 

17

 

 Cluster B

11

 

13

 

11

 

CDH1+TOP2A (Cluster D, CDH1 high and TOP2A low)c

 

0.1

 

0.01

 

0.01

 Cluster C

15

 

39

 

42

 

 Cluster D

48

 

81

 

81

 

Histologic grade (low (Grade 1–2) vs high (Grade 3))d

 

0.97

 

0.01

 

0.01

 Low grade

6

 

59

 

59

 

 High grade

12

 

20

 

21

 

Growth pattern (papillary vs nonpapillary)

 

0.58

 

0.01

 

0.01

 Papillary

11

 

12

 

13

 

 Nonpapillary

17

 

52

 

52

 

Invasion (superficial (TaT1a) vs invasive (T1bT4))e

 

0.64

 

0.01

 

0.01

 Superficial

8

 

70

 

55

 

 Invasive

11

 

29

 

15

 
  1. *P-values of Kaplan–Meier log-rank test.
  2. aThe expression for each gene was determined by immunohistochemical analysis in tissue microarray and represents the comparison between the tumor groups expressing low and high level of the gene with the median value of REL differentiating low and high expression levels.
  3. bClusters A and B were defined on the basis of differential expressions of six genes in tissue microarray as depicted in Figure 6a.
  4. cUsing immunohistochemical expression levels of CDH1 and TOP2A tumors were classified into two groups—(C) characterized by high expression levels of CDH1 and low expression levels of TOP2A and (D) characterized by overexpression of TOP2A and low expression of CDH1 as shown in Figure 6b.
  5. dHistologic grading was performed according to WHO grading system for bladder tumors.
  6. eTumors were staged according to the TNM classification of malignant tumors with T1a/T1b substaging.
  7. The feature that correlates with aggressive clinical behavior is shown in parentheses.