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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Clin Exp Metastasis. 2015 Oct 27;33(1):53–62. doi: 10.1007/s10585-015-9757-7

Table 5.

Trade-offs between strength and precision of cut-point/time-to-death association and number of patients with low or high expression, by stage distribution and 5-year risk of death, for multiple cut points of E-cadherin weighted average expression

Cut point 0.52b
Cut point 0.60
Cut point 0.85
Cox model estimatea HR
2.57
95 % CI (CLR)
1.10, 6.03 (5.48)
HR
2.40
95 % CI (CLR)
1.29, 4.49 (3.48)
HR
1.75
95 % CI (CLR)
0.99, 3.08 (3.11)
Stage Low High Low High Low High
    Local (n = 99) 6 93 16 83 56 43
    Regional (n = 66) 5 61 11 55 41 25
    Distant (n = 23) 0 23 1 22 11 12
Mortality risk
    Died within 5 years (n = 62) (x) 7 55 14 48 42 20
    Total at risk (n = 188) (y) 11 177 28 160 108 80
    5-year risk of death post-surgery (%) (x/y) 64 31 50 30 39 25
Mortality Risk Effect estimatesc Estimate 95 % CI Estimate 95 % CI Estimate 95 % CI
Risk difference (%) 33 3, 62 20 0, 40 14 1, 27
Risk ratio 2.05 1.25, 3.37 1.67 1.07, 2.59 1.56 0.99, 2.43

CLR Confidence limit ratio (upper limit/lower limit)

E-cadherin measured as a weighted average (weighted by area analyzed) of continuous tumor core average intensities (0–3) prior to dichotomization. Of 190 subjects, 2 had missing data for E-cadherin, but multiple imputation enabled retention of these 2 in Cox models

a

For effect of dichotomous E-cadherin expression (low versus high) on time-to-death, adjusted for age (continuous), TNM stage (local/regional/distant), neoadjuvant chemotherapy (yes/no), and neoadjuvant radiation treatments (yes/no)

b

Statistically-optimal cut point by best model fit

c

Unadjusted comparisons of low versus high expression status