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Published in: BMC Cancer 1/2014

Open Access 01-12-2014 | Research article

Inclusion of KI67 significantly improves performance of the PREDICT prognostication and prediction model for early breast cancer

Authors: Gordon C Wishart, Emad Rakha, Andrew Green, Ian Ellis, Hamid Raza Ali, Elena Provenzano, Fiona M Blows, Carlos Caldas, Paul DP Pharoah

Published in: BMC Cancer | Issue 1/2014

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Abstract

Background

PREDICT (http://​www.​predict.​nhs.​uk) is a prognostication and treatment benefit tool for early breast cancer (EBC). The aim of this study was to incorporate the prognostic effect of KI67 status in a new version (v3), and compare performance with the Predict model that includes HER2 status (v2).

Methods

The validation study was based on 1,726 patients with EBC treated in Nottingham between 1989 and 1998. KI67 positivity for PREDICT is defined as >10% of tumour cells staining positive. ROC curves were constructed for Predict models with (v3) and without (v2) KI67 input. Comparison was made using the method of DeLong.

Results

In 1274 ER+ patients the predicted number of events at 10 years increased from 196 for v2 to 204 for v3 compared to 221 observed. The area under the ROC curve (AUC) improved from 0.7611 to 0.7676 (p = 0.005) in ER+ patients and from 0.7546 to 0.7595 (p = 0.0008) in all 1726 patients (ER+ and ER-).

Conclusion

Addition of KI67 to PREDICT has led to a statistically significant improvement in the model performance for ER+ patients and will aid clinical decision making in these patients. Further studies should determine whether other markers including gene expression profiling provide additional prognostic information to that provided by PREDICT.
Appendix
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Metadata
Title
Inclusion of KI67 significantly improves performance of the PREDICT prognostication and prediction model for early breast cancer
Authors
Gordon C Wishart
Emad Rakha
Andrew Green
Ian Ellis
Hamid Raza Ali
Elena Provenzano
Fiona M Blows
Carlos Caldas
Paul DP Pharoah
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2014
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/1471-2407-14-908

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