Machine learning predicts rapid relapse of triple negative breast cancer
Y. Zhang, W. Nock, M. Wyse, Z. Weber, E. Adams, S. Stockard, D. Tallman, S. Asad, E. P. Winer, N. U. Lin, M. Cherian, M. Lustberg, B. Ramaswamy, S. Sardesai, J. Vandeusen, N. Williams, R. Wesolowski, D. G. Stover
Abstract
PurposeMetastatic relapse of triple-negative breast cancer (TNBC) within 2 years of diagnosis is associated with particularly aggressive disease and a distinct clinical course relative to TNBCs that relapse beyond 2 years. We hypothesized that rapid relapse TNBCs (rrTNBC; metastatic relapse or death 2 years).\n\nPatients and MethodsWe identified 453 primary TNBCs from three publicly-available datasets and characterized each as rrTNBc, lrTNBC, or no relapse (nrTNBC: no relapse/death with at least 5 years follow-up). We compiled primary tumor clinical and multi-omic data, including transcriptome (n=453), copy number alterations (CNAs; n=317), and mutations in 171 cancer-related genes (n=317), then calculated published gene expression and immune signatures.\n\nResultsPatients with rrTNBC were higher stage at diagnosis (Chi-square p0.75.\n\nConclusionsWe provide a new approach to define TNBCs based on timing of relapse. We identify distinct clinical and genomic features that can be incorporated into machine learning models to predict rapid relapse of TNBC.
02 /Specification & Classification
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