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Incorporating progesterone receptor expression into the PREDICT breast prognostic model

  • ABCTB Investigators
  • , kConFab Investigators
  • , kConFab Investigators
  • University of Cambridge
  • Antoni van Leeuwenhoek Hospital
  • Cancer Council Victoria
  • Melbourne School of Population and Global Health
  • Monash University
  • Institute of Cancer Research
  • University of California at Los Angeles
  • Friedrich-Alexander University Erlangen-Nürnberg
  • National Cancer Institute (NCI)
  • University of Toronto
  • University of California at Irvine
  • University of Helsinki
  • Örebro University
  • Copenhagen University Hospital – Herlev and Gentofte
  • University of Copenhagen
  • European Institute of Oncology
  • Universidad de la Sabana
  • German Cancer Research Center
  • Heidelberg University 
  • University of Utah School of Medicine
  • Oncology and Genetics Unit
  • Seoul National University
  • Seoul National University Cancer Research Institute
  • The University of Sydney
  • Mayo Clinic Rochester, MN
  • University of Sheffield
  • Karolinska Institutet
  • Leiden University
  • Hannover Medical School
  • University of Westminster
  • University of Southampton, Faculty of Medicine
  • Ulm University
  • University of Manchester
  • Manchester University NHS Foundation Trust
  • University of Edinburgh
  • KU Leuven
  • Peter Maccallum Cancer Centre
  • Complejo Hospitalario Universitario de Santiago
  • Moores Cancer Center
  • Hospital Clínico San Carlos de Madrid
  • Centro de Investigación en Red de Enfermedades Raras
  • Keck School of Medicine of USC
  • Wythenshawe Hospital
  • National University of Singapore
  • MOH Holdings Pte Ltd.
  • University of Melbourne
  • Erasmus MC Cancer Institute
  • Kaohsiung Municipal Hsiao-Kang Hospital
  • Aichi Cancer Center Hospital and Research Institute
  • Nagoya University
  • Pomeranian Medical University in Szczecin
  • Stanford University School of Medicine
  • Stanford University
  • University of Oslo
  • Hong Kong Hereditary Breast Cancer Family Registry
  • The University of Hong Kong
  • Hong Kong Sanatorium & Hospital
  • VIB Department of Molecular Microbiology
  • Agency for Science, Technology and Research, Singapore
  • University of Malaya
  • University Health Network
  • Memorial Sloan-Kettering Cancer Center
  • Centre for Biomedical Research on Rare Diseases (CIBERER)
  • American Cancer Society
  • University of Oulu
  • Laboratory of Cancer Genetics and Tumor Biology
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • Technion-Israel Institute of Technology
  • Hospital Puerta de Hierro
  • University Hospital of Larissa
  • King's College London
  • Academia Sinica - Institute of Biomedical Sciences
  • China Medical University Taichung
  • The University of Auckland
  • Cancer Research Malaysia
  • Erasmus University Rotterdam

Producción: Contribución a una revistaArtículorevisión exhaustiva

16 Citas (Scopus)

Resumen

Background: Predict Breast (www.predict.nhs.uk) is an online prognostication and treatment benefit tool for early invasive breast cancer. The aim of this study was to incorporate the prognostic effect of progesterone receptor (PR) status into a new version of PREDICT and to compare its performance to the current version (2.2). Method: The prognostic effect of PR status was based on the analysis of data from 45,088 European patients with breast cancer from 49 studies in the Breast Cancer Association Consortium. Cox proportional hazard models were used to estimate the hazard ratio for PR status. Data from a New Zealand study of 11,365 patients with early invasive breast cancer were used for external validation. Model calibration and discrimination were used to test the model performance. Results: Having a PR-positive tumour was associated with a 23% and 28% lower risk of dying from breast cancer for women with oestrogen receptor (ER)-negative and ER-positive breast cancer, respectively. The area under the ROC curve increased with the addition of PR status from 0.807 to 0.809 for patients with ER-negative tumours (p = 0.023) and from 0.898 to 0.902 for patients with ER-positive tumours (p = 2.3 × 10−6) in the New Zealand cohort. Model calibration was modest with 940 observed deaths compared to 1151 predicted. Conclusion: The inclusion of the prognostic effect of PR status to PREDICT Breast has led to an improvement of model performance and more accurate absolute treatment benefit predictions for individual patients. Further studies should determine whether the baseline hazard function requires recalibration.

Idioma originalInglés
Páginas (desde-hasta)178-193
Número de páginas16
PublicaciónEuropean Journal of Cancer
Volumen173
DOI
EstadoPublicada - sept 2022

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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