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Integrated tumor identification and automated scoring minimizes pathologist involvement and provides new insights to key biomarkers in breast cancer

Authors :
Gareth Irwin
Darragh G. McArt
Maurice B Loughrey
Gerald Li
David P Boyle
Stephen McQuaid
Peter W. Hamilton
D. Paul Harkin
Peter Bankhead
Jacqueline James
Manuel Salto-Tellez
José A Fernández
Source :
Bankhead, P, Fernández, J A, McArt, D G, Boyle, D P, Li, G, Loughrey, M B, Irwin, G W, Harkin, D P, James, J A, McQuaid, S, Salto-Tellez, M & Hamilton, P W 2017, ' Integrated tumor identification and automated scoring minimizes pathologist involvement and provides new insights to key biomarkers in breast cancer ', Laboratory investigation, vol. 98, no. 1, pp. 15-26 . https://doi.org/10.1038/labinvest.2017.131, Bankhead, P, Fernández, J A, McArt, D G, Boyle, D P, Li, G, Loughrey, M B, Irwin, G W, Harkin, D P, James, J A, McQuaid, S, Salto-Tellez, M & Hamilton, P W 2018, ' Integrated tumor identification and automated scoring minimizes pathologist involvement and provides new insights to key biomarkers in breast cancer ', Laboratory investigation, vol. 98, pp. 15-26 . https://doi.org/10.1038/labinvest.2017.131
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Digital image analysis (DIA) is becoming central to the quantitative evaluation of tissue biomarkers for discovery, diagnosis and therapeutic selection for the delivery of precision medicine. In this study, automated DIA using a new purpose-built software platform (QuPath) is applied to a cohort of 293 breast cancer patients to score five biomarkers in tissue microarrays (TMAs): ER, PR, HER2, Ki67 and p53. This software is able to measure IHC expression following fully automated tumor recognition in the same immunohistochemical (IHC)-stained tissue section, as part of a rapid workflow to ensure objectivity and accelerate biomarker analysis. The digital scores produced by QuPath were compared with manual scores by a pathologist and shown to have a good level of concordance in all cases (Cohen's κ>0.6), and almost perfect agreement for the clinically relevant biomarkers ER, PR and HER2 (κ>0.86). To assess prognostic value, cutoff thresholds could be applied to both manual and automated scores using the QuPath software, and survival analysis performed for 5-year overall survival. DIA was shown to be capable of replicating the statistically significant stratification of patients achieved using manual scoring across all biomarkers (P

Details

ISSN :
00236837
Volume :
98
Database :
OpenAIRE
Journal :
Laboratory Investigation
Accession number :
edsair.doi.dedup.....db290c22309300a431c451586b672c5e