Evaluation of biomarker panels for early stage ovarian cancer detection and monitoring for disease recurrence

Objective. To determine the utility of novel combinations of biomarkers. Using both a one-step and two-step assay format, to distinguish serum of early ovarian cancer patients from that of healthy controls and to discern the utility of these biomarkers in a monitoring capacity. Methods. For ovarian cancer detection. HE4. Glycodelin. MMP7, SLPI. Plau-R, MUC1, Inhibin A. PAI-1, and CA125 were evaluated in a cohort of 200 women with ovarian cancer and 396 healthy ape-matched controls. Each biomarker was assessed by serum-based immunoassays utilizing novel monoclonal antibody pairs or commercial kits. For detection of disease recurrence, HE4. Glycodelin, MMP7 and CA125 were evaluated in 260 samples from 30 patients with OC monitored longitudinally after diagnosis. Results. Based upon ROC curve analysis, the sensitivity/specificity of specific biomarker combination algorithms ranged from 59.0%/99.7% to 80.5%/96.5% for detection of early stage ovarian cancer and 76.9%/99.7% to 89.2%/97.2% for detection of late stage cancer. In monitoring evaluation of 27 patients who experienced recurrence of OC. sensitivity for predicting recurrence was 100% for the biomarker panel and 96% for CA 125. At least one of the panel biomarkers was elevated earlier (range 6-69 weeks) than CA 125 and prior to clinical evidence of recurrence in 14/27 (52%) patients. Conclusions. We have developed and demonstrated the utility of several one- and two-step multi-marker combinations with acceptable test characteristics for possible use in an ovarian cancer screening population. A subset of this panel may also provide adjunctive information to rising CA125 levels in disease monitoring. (C) 2008 Elsevier Inc. All rights reserved.