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Table 2 Bayesian latent class estimates of sensitivity and specificity of E-cadherin measurements in colorectal primary tumor cancer cells to assess cancer cell detachment from primary tumor (n = 188)

From: Diagnostic accuracy and prediction increment of markers of epithelial-mesenchymal transition to assess cancer cell detachment from primary tumors

 

Fully

Fully

Partial Dependent Models

 

Independent

Dependent

PDM 1

PDM 2

PDM 3

PDM 4

PDM 5

PDM 6

Constraints Set to 0

All

None

Se(Ecad)

Se(LN)

Se(RI)

Se(Ecad)

Se(Ecad)

Se(LN)

   

Sp(Ecad)

Sp(LN)

Sp(RI)

Sp(Ecad)

Sp(Ecad)

Sp(LN)

      

Se(LN)

Se(RI)

Se(RI)

      

Sp(LN)

Sp(RI)

Sp(RI)

E-cadherin Variable

Se

Sp

Se

Sp

Se

Sp

Se

Sp

Se

Sp

Se

Sp

Se

Sp

Se

Sp

Dichotomized at 0.52

47

28

54

44

52

49

52

42

53

44

47

28

52

48

52

43

Dichotomized at 0.60

49

22

57

43

53

40

53

41

53

43

49

22

53

40

52

42

Dichotomized at 0.85

46

14

53

43

52

41

52

42

53

43

46

14

52

41

52

41

  1. Cellular membrane E-cadherin expression measured as protein in primary tumor cancer cells on a continuous average intensity scale (0–3), then dichotomized at the indicated cut point (coded EMT positive versus EMT negative). LN and RI were each coded as dichotomous positive versus negative. LN and RI each assigned the same prior of Se 60–70% and Sp 95–99%. For all dichotomous test variables, positive results mean evidence supporting detachment of cancer cells from the primary tumor and negative results mean no evidence of detachment. All Se and Sp estimates are reported as percentages
  2. Ecad E-cadherin, LN lymph node evaluation, PDM partial dependent model, RI radiologic imaging, Se sensitivity, Sp specificity