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. 2004 Jan 20;90(2):423–429. doi: 10.1038/sj.bjc.6601534

Table 2. COX-2 expression and clinicopathological parameters in women with DCIS (n=187) and IBC (n=65).

Parameter Number % COX-2 +ve P-valuea
DCIS
Age (years)
 <50 35 62% 0.34
 ⩾50 152 69%  
Nuclear grade
 Low 27 44%  
 Intermediate 64 64% 0.003
 High 96 75%  
ER status
 Positive 111 58% 0.003
 Negative 75 80%  
Ki67 cell proliferation
 <10% 93 55% <0.0001
 ⩾10% 90 79%  
HER-2 status
 Positive 102 82% <0.0001
 Negative 85 48%  
 
Invasive cancer
Age (years)
 <50 23 64% 0.67
 ⩾50 42 62%  
Nuclear grade
 I 17 53%  
 II 17 58% 0.43
 III 21 71%  
ER status
 Positive 40 50% 0.005
 Negative 25 84%  
Ki67 cell proliferation
 <10% 29 50% 0.04
 ⩾10% 36 74%  
HER-2 status
 Positive 29 79% 0.014
 Negative 36 50%  

Age above and below 50 years was used to separate pre- and postmenopausal patients crudely. Oestrogen receptor positivity was a tumour with ⩾5% nuclei expressing the ER receptor for both DCIS and IBC. A comparison of COX-2 positivity with Ki67 cell proliferation above and below 10% was used because the median DCIS cell proliferation was approximately 10%. HER-2 positivity was an immunostaining score of ⩾2+ (reference laboratory standard). Categorical variables were compared differences using the χ2 test. COX-2=cyclooxygenase type-2; DCIS=ductal carcinoma in situ; IBC=invasive breast cancer; ER=oestrogen receptor.

a

χ2 test.