Table 5 Group 4: Immunohistochemical expression of TOPK (patchy or diffuse) and clinicopathological and molecular features in metastatic colorectal cancer patients treated with anti-EGFR therapy

From: Prognostic and predictive value of TOPK stratified by KRAS and BRAF gene alterations in sporadic, hereditary and metastatic colorectal cancer patients

 

N (%)

Clinicopathological features

Patchy

Diffuse

P -value

Age (years)

 Mean, range

65.7, 48–82

60.7, 26–79

0.113

Gender

 Female

8 (36.4)

9 (39.1)

0.848

 Male

14 (63.6)

14 (60.9)

 

Clinical response

 Progressive disease

13 (59.1)

10 (43.5)

0.528

 Partial response

4 (18.2)

7 (30.4)

 

 Stable disease

5 (22.7)

6 (26.1)

 

KRAS codon 12 and 13

 Wild type

13 (59.1)

19 (82.6)

0.082

 Mutation

9 (40.9)

4 (17.4)

 

BRAF codon 600

 Wild type

20 (90.9)

21 (91.3)

1.0

 Mutation

2 (9.1)

2 (8.7)

 

KRAS/BRAF

 Both wild type

11 (50.0)

17 (73.9)

0.098

KRAS or BRAF mutation

11 (50.0)

6 (26.1)

 

Microsatellite status

 Stable/low

22 (100.0)

22 (100.0)

 

 High

   

EGFR amplification

 No copy number gain

4 (19.1)

3 (13.0)

0.693

 Copy number gain

17 (81.0)

20 (87.0)

 

PI3KCA

 Loss

19 (86.4)

20 (87.0)

1.0

 Overexpression

3 (13.6)

3 (13.0)

 

PTEN

 Loss

11 (50.0)

6 (26.1)

0.09

 Overexpression

11 (50.0)

17 (73.9)

 
 

Rate (95% CI)

 

5-year survival time

 All patients

34.5 (11–60)

13.5 (1–40)

0.473

 Either KRAS or BRAF mutation

18.2 (3–44)

16.7 (0–51)

0.887

 Both wild type KRAS and BRAF

66.7 (5–95)

15.3 (1–45)

0.018

 Stable disease or response

100

31.3 (8–59)

0.01

  1. Abbreviations: CI=confidence interval; EGFR=epidermal growth factor receptor; N=frequency; TOPK=T-cell-originated protein kinase.