The AUC of MDK was not statistically significantly different from the AUC of AGR2 (p > 0.05). A binomial classification algorithm was developed by subjecting the observed plasma concentrations for MDK, AGR2 and CA125 to stochastic gradient boosted logistic regression analysis [19]. A ρP value was calculated for each patient set of biomarkers and used to generate a ROC curve (Figure 2). The AUC for the multi-analyte panel (0.988

± 0.011) was significantly greater than that for MDK (p < 0.001), AGR2 selleck kinase inhibitor (p = 0.001) and CA125 (p = 0.038) (Figure 3). The sensitivity and specificity of the multi-analyte algorithm were 95.2 and 97.7%, respectively. Within the study cohort, CA125 displayed a sensitivity and specificity of 87.0 and 94.6%, respectively. Selleckchem CP673451 Figure 2 Predicted posterior probability values

(ρP). Values were generated by multivariate modelling for each patient set of biomarkers for Case and Control cohorts. Figure 3 ROC curve comparison. ROC curves are displayed for the multi-analyte algorithm (midkine, AGR2 and CA125) and CA125 alone. The AUC (± SEM) for the multi-analyte panel (black diamond) (0.988 ± 0.010) was significantly greater than that of CA125 alone (black circle) (0.934 ± 0.030, p = 0.035). Discussion The aims of this study were: to characterise and compare plasma concentrations of midkine (MDK) in normal Captisol cost healthy women with concentrations observed in women with ovarian cancer; and to establish and compare the performance of MDK with that of anterior gradient 2 protein (AGR2) and CA125 in the development of multi-analyte classification algorithms for ovarian cancer. A retrospective, case-control Amisulpride study was conducted to compare the diagnostic performance (as measured by AUC) of plasma ir MDK and ir AGR2 individually or

in combination with CA125 with the performance of CA125 alone. Biomarker plasma concentrations were quantified in normal healthy women and women with confirmed ovarian cancer. The data obtained confirm the utility of both MDK and AGR2 as plasma biomarkers for ovarian cancer and, when combined in a multi-analyte panel, significantly improve the diagnostic efficiency of CA125. The median plasma concentrations of both ir MDK and ir AGR2 were significantly greater in women with ovarian cancer (909 pg/ml and 765 pg/ml, respectively n = 46) than in normal healthy women (383 pg/ml and188 pg/ml, respectively n = 61) (p < 0.001). There is a paucity of data characterising the plasma concentrations of MDK in ovarian cancer patients. Salama et al. (2006) [20] reported a similar change in serum MDK concentrations in 15 women with ovarian carcinoma (i.e. > 500 pg/ml) and 49 controls (i.e. < 500 pg/ml) to those concentrations reported in this study. Within the present study cohort, plasma concentrations of MDK and AGR2 were not significantly altered by tumor type or stage of disease.