Abstract 2105: Cell-free DNA fragments inform epigenomic mechanisms for early detection of breast cancer

Abstract

Introduction: Chromatin accessibility and cell-free DNA fragmentation patterns can be used to identify epigenomic mechanisms (Sharma et al. 2010) and infer cell-types contributing to cfDNA in pathological states such as cancer (Snyder et al. 2016; Ulz et al. 2017). We describe results from a novel blood-based cell-free DNA (cfDNA) assay using epigenomic signatures that have high sensitivity for detecting early stages of breast cancer, a cancer type that is characterized by low tumor burden (Phallen et al. 2017). We present the results from a prospective, case-control study demonstrating improved sensitivity to the screening mammogram and other published blood-based assays. Methods: Assay performance was evaluated using a case-control study design enrolling 123 total subjects (58% Healthy, 18% Stage I, 13% Stage II, 11% Stage III). Cases were defined as subjects with a confirmatory diagnosis of invasive breast cancer, at any stage, by tissue biopsy. Controls were composed of subjects with either a negative finding by mammography (BI-RADS 1 or 2) or self-declared cancer-free. Whole blood samples were collected in Streck BCT tubes and shipped to a central laboratory for processing. Total cell-free DNA was extracted from plasma and prepped for next-generation sequencing. Sequencing libraries were enriched using a custom panel targeting genomic regions with distinct epigenomic activity in breast cancer. We trained a neural net to predict regulatory events in each of these regions, and then identified those events that were predictive of the presence of breast cancer. Final classification was performed by logistic regression over the predicted regulatory events. Results: Performance was tested using a held-out test set and achieved an overall sensitivity of 92.5% (95% CI: 88.1%, 97%) at specificity of 88.9% with an overall AUC of 95.8%. Performance of screening mammography is reported to be 86.9% (95% CI: 86.3%, 87.6%) sensitive at 88.9% specificity on data obtained from six Breast Cancer Surveillance Consortium (BCSC) registries on 792808 women (Lehman et al. 2017). Conclusion: These results support the utility for detecting epigenomic signals from cell-free DNA to enhance early detection of breast cancer. A prospective breast cancer screening study in a larger cohort is needed to further validate performance. Citation Format: Erik Gafni, Adam Harvey, Artur Jaroszewicz, Omid Shams Solari, Jane Landolin, Mouadh Barbirou, Amanda Miller, Peter J. Tonellato, Anshul Kundaje, Stefanie S. Jeffrey, Christina Curtis, George W. Sledge, Paul Giresi, Nathan Boley. Cell-free DNA fragments inform epigenomic mechanisms for early detection of breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2105.