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. 2014 Nov 4;112(1):162–166. doi: 10.1038/bjc.2014.566

Table 1. Selected baseline characteristics of EOC cases and matched controls at enrolment in the EPIC study.

  Cases (n=565)a Controls (n=1097)a P-valueb
Age at blood donationc 57.0 (33.6–80.7) 56.9 (33.6–79.3)  
Age at diagnosis 63.6 (37.4–86.5)    
Lag time between blood donation and diagnosis 6.7 (0–16)    
Menopausal status at blood donationb
 Pre 112 (20%) 219 (20%)  
 Post 453 (80%) 878 (80%)  
Age at menopaused 50 (32–60) 50 (30–59) 0.03
Ever full-term pregnancy     <0.01
 No 95 (17%) 124 (12%)  
 Yes 448 (83%) 935 (88%)  
OC use     < 0.01
 Never 349 (62%) 594 (54%)  
 Ever 214 (38%) 498 (46%)  
HRT useb     0.57
 Never 452 (87%) 867 (86%)  
 Ever 69 (13%) 145 (14%)  
Histology
Serous 302 (53%)    
Mucinous 41 (7%)    
Endometrioid 66 (12%)    
Clear Cell 28 (5%)    
NOS 99 (18%)    
Other 29 (5%)    
Gradee,f
Low grade 35 (10%)    
High grade 308 (90%)    
Stagee,g
Low stage 76 (15%)    
High stage 420 (85%)    
Type I/IIe
Type I 67 (22%)    
Type II 242 (78%)    
IGF-I (nmol l−1) h 13.98 (13.39–14.6) 14.06 (13.63–14.5) 0.26

Abbreviations: EOC=epithelial ovarian cancer; EPIC=European Prospective Investigation into Cancer and Nutrition; HRT=hormone replacement therapy; IGF-I=insulin-like growth factor I.

Values are shown as median (range) or number (percentage).

a

Cases and controls in both study phases were matched on: study recruitment centre, age at blood donation (±6 months), time of the day of blood collection (±1 h), fasting status (<3 h, 3–6 h, >6 h) and menopausal status at blood collection (premenopausal, perimenopausal and postmenopausal), as well as menstrual cycle phase for premenopausal women (‘early follicular' (days 0–7 of the cycle), ‘late follicular' (days 8–11), ‘peri-ovulatory' (days 12–16), ‘mid-luteal' (days 20–24) and ‘other luteal' (days 17–19 or days 25–40 ). Cases missing data on the phase of menstrual cycle were matched to controls with missing information on menstrual cycle phase.

b

Among postmenopausal women only.

c

Matching factor.

d

Differences between cases and matched controls based on conditional logistic regression.

e

Percentages presented among women with data on tumour characteristics. Percentage of missing data: grade (39%), stage (12%) and type I/II status (45%).

f

Low-grade tumours: well differentiated tumours; high-grade tumours: moderately, poorly or undifferentiated tumours.

g

Low-stage tumours: localised tumours; high-grade tumours: regional metastatic or distant metastatic tumours.

h

Differences in IGF-I concentrations between cases and matched controls based on geometric mean (95% confidence interval); values from each study phase are standardised to a mean of 0 for analyses.