Skip to main content
. 2012 Oct 25;107(12):1997–2004. doi: 10.1038/bjc.2012.477

Table 2. Clinico-pathological variables related to KRAS gene expression analysed by qPCR for 161 patients.

Variable High expression, n (%) Low expression, n (%) P -value
Age
 ⩽66 20 (21.5) 74 (78.5) 0.2
 >66 21 (31.3) 46 (68.7)  
 
BMI a
 ⩽25 14 (25.5) 41 (74.5) 0.7
 >25 27 (28.1) 69 (71.9)  
 
FIGO stage b
 I–II 28 (21.9) 100 (78.1) 0.04
 III–IV 13 (39.4) 20 (60.6)  
 
Histological type
 Endometroid 25 (18.9) 107 (81.1) <0.001
 Non-endometroid 16 (55.2) 13 (44.8)  
 
Grade c
 Low-medium 17 (16) 89 (84) <0.001
 High 24 (44.4) 30 (55.6)  
 
Lymph node d
 Negative 28 (22.2) 98 (78.8) 0.02
 Positive 10 (52.6) 9 (47.4)  
 
Ploidy e
 Diploid 19 (19) 80 (81) 0.001
 Aneuploid 18 (50) 18 (50)  
 
ERα f
 Positive 21 (17) 101 (83) <0.001
 Negative 19 (53) 17 (47)  
 
PR g
 Positive 20 (16) 104 (84) <0.001
 Negative 19 (56) 15 (44)  
 
PIK3CA mut h
 N.m.d 33 (25.6) 96 (74.4) 0.47
 Mutated 6 (28.6) 15 (78.4)  
 
P53 i
 High 20 (57.1) 15 (42.9) <0.001
 Low 17 (16.5) 86 (83.5)  

Abbreviations: BMI=body mass index; ER=oestrogen receptor; FIGO=International Federation of Gynaecology and Obstetrics; KRAS=Homo sapiens v-Ki-ras2 Kirsten rat sarcoma viral oncogenes homologue; N.m.d=no mutations detected; PR=progesterone receptor.

The P-value was based on the χ2-test or Fisher’s exact test as indicated.

Data missing: a10, c1, d16, e26, f3, g3, h11, i23.

b

FIGO 2009 criteria.