Abstract

Biomarkers for early detection of epithelial ovarian cancer (EOC) are urgently needed. Patients can generate antibodies to tumor-associated antigens (TAAs). We tested multiplex detection of antibodies to candidate ovarian TAAs and statistical modeling for discrimination of sera of EOC patients and controls. Binding of serum antibody of women with EOC or healthy controls to candidate TAA-coated microspheres was assayed in parallel. A Bayesian model/variable selection approach using Markov Chain Monte Carlo computations was applied to these data, and serum CA125 values, to determine the best predictive model. The selected model was subjected to area under the receiver-operator curve (AUC) analysis. The best model generated an AUC of 0.86 [95% confidence interval (95% CI), 0.78-0.90] for discrimination between sera of EOC patients and healthy patients using antibody specific to p53, NY-CO-8, and HOXB7. Inclusion of CA125 in the model provided an AUC of 0.89 (95% CI, 0.84-0.92) compared with an AUC of 0.83 (95% CI, 0.81-0.85) using CA125 alone. However, using TAA responses alone, the model discriminated between independent sera of women with nonmalignant gynecologic conditions and those with advanced-stage or early-stage EOC with AUCs of 0.71 (95% CI, 0.67-0.76) and 0.70 (95% CI, 0.48-0.75), respectively. Serum antibody to p53 and HOXB7 is positively associated with EOC, whereas NY-CO-8-specific antibody shows negative association. Bayesian modeling of these TAA-specific serum antibody responses exhibits similar discrimination of patients with early-stage and advanced-stage EOC from women with nonmalignant gynecologic conditions and may be complementary to CA125.

Highlights

  • Conventional treatment has limited efficacy against advancedstage epithelial ovarian cancer (EOC), whereas >80% patients with early-stage disease survive 5 years after diagnosis

  • To explore the utility of autologous serum antibody specific to particular tumor-associated antigens (TAAs) as an additional tool for discrimination of sera from cancer patients and healthy women, we generated recombinant protein from 13 markers identified previously as candidate TAAs and selected 5 presumptive control reagents. Sera from both healthy women and EOC patients were tested in parallel for reactivity to all 18 panel elements

  • We tested sera of 23 healthy women from M. D. Anderson Cancer Center (MDACC) as controls and sera from 59 stage III/IV ovarian cancer patients obtained at University of Louisville School of Medicine (ULSM) and 27 from MDACC as cases, respectively

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Summary

Introduction

Conventional treatment has limited efficacy against advancedstage epithelial ovarian cancer (EOC), whereas >80% patients with early-stage disease survive 5 years after diagnosis. Because there is no diagnostic tool for reliable screening and detection of premalignant or localized ovarian cancer, 70% of patients with ovarian cancer have advanced disease on initial diagnosis [1]. Measurement of serum CA125 levels was approved as a prognostic indicator to monitor disease recurrence [2]. Elevated levels of CA125 are detected in >90% of sera of disseminated ovarian cancer cases (stages II-IV) but in only 50% of patients with stage I disease [2]. The CA125 assay is inappropriate as a ‘‘stand-alone’’ population screen for early-stage ovarian cancer, its positive predictive value can be improved by combination with other screening tools (e.g., serial measurements, transvaginal sonography, or combinations with other markers and statistical modeling)

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