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Sensitive and Specific Early-Stage Breast Cancer Detection using Deep Proteome Profiling from Plasma

Horrmann, A.; Travadi, Y.; Carey, J.; Boytim, E.; Mallery, K.; Schaap, G.; Rungkittikhun, C.; Kamalanathan, K. J.; Bristow, N. R.; Galeano-Garces, C.; Groth, A.; Ball, H.; Hesch, A. R.; Advani, P.; Hwang, J.; Konety, B. R.; Drake, J. M.

2025-12-09 oncology
10.64898/2025.12.07.25341735 medRxiv
Show abstract

Proteome-guided liquid biopsy tests hold immense promise for the future of early cancer detection. Our previous published work has shown strong performance identifying early-stage breast cancer patients using prospectively collected, case-controlled samples. Here, we analyzed the plasma proteome of 1,259 biobanked samples consisting of healthy women and women with breast cancer. The Astrin Biosciences breast cancer early detection test is a laboratory developed test (LDT) that uses a protein-based machine learning classifier to identify breast cancer with high accuracy. The classifier was trained on 845 women, comprising of 466 healthy and 379 with newly diagnosed, treatment naive breast cancer and validated on 397 women (195 healthy and 202 breast cancer). All plasma samples were processed in a blinded manner coupled with semi-quantitative, label-free mass spectrometry (MS)-based analysis. The validation performance achieved 92.3% specificity, 92.6% sensitivity and an AUC of 0.975. Sensitivity remained high across all breast cancer stages and pathological and molecular subtypes. Gene set enrichment analyses (GSEA) identified epithelial-to-mesenchymal transition (EMT) and PI3K-AKT signaling as enriched in the breast cancer samples, highlighting that our test can identify cancer-related proteins in early-stage patients. A simulated population demonstrates the utility of our test as a supplement to mammography, detecting nearly all (93%) breast cancers missed by mammography and reducing the number of false positives relative to MRI and Contrast-Enhanced Mammography (CEM) by >10-fold. Overall, our proteomic data demonstrates high sensitivity and specificity in women with breast cancer, especially at early stages, and is a favorable supplemental test post mammogram.

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