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Abstract Background: Although several gene expression-based assays are validated for informing prognosis and treatment decision-making for breast cancer (BC) patients, their uptake has been hampered by technical complexities and cost, particularly in underrepresented and low-resource settings. Here, we explored whether machine learning-based features on standard hematoxylin and eosin (H0.0001), and according to RS categories within both ER+ (P=0.009) and ER- (P=0.006) BC subtypes in the validation set. Conclusion: H 2024 Sep 21-24; Los Angeles, CA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2024;33(9 Suppl):Abstract nr C022.
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Abubakar et al. (Sat,) studied this question.
www.synapsesocial.com/papers/68e57c1db6db64358751b48e — DOI: https://doi.org/10.1158/1538-7755.disp24-c022
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Mustapha Abubakar
Amber N. Hurson
Thomas U. Ahearn
Cancer Epidemiology Biomarkers & Prevention
University of North Carolina at Chapel Hill
National Cancer Institute
University of Calgary
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