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SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN

BACKGROUND: Breast cancer (BC) is a leading cause of mortality and the most frequent malignancy in women; most deaths are due to metastatic disease, expressly brain metastases (BM). Currently, there is no biomarker or a prediction model to accurately predict BM. OBJECTIVE: To generate a BM predictio...

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Autores principales: Cacho-Díaz, Bernardo, Reynoso-Noveron, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402393/
http://dx.doi.org/10.1093/noajnl/vdad070.092
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author Cacho-Díaz, Bernardo
Reynoso-Noveron, Nancy
author_facet Cacho-Díaz, Bernardo
Reynoso-Noveron, Nancy
author_sort Cacho-Díaz, Bernardo
collection PubMed
description BACKGROUND: Breast cancer (BC) is a leading cause of mortality and the most frequent malignancy in women; most deaths are due to metastatic disease, expressly brain metastases (BM). Currently, there is no biomarker or a prediction model to accurately predict BM. OBJECTIVE: To generate a BM prediction model from variables acquired at BC diagnosis. METHODS: A retrospective cohort of BC women diagnosed from 2009 to 2020 at a single center was divided into training (TD) and validation datasets (VD). The TD was used to generate a multivariable prediction model. The modeĹs performance was measured applying the area under the curve (AUC), C-statistic, and the Akaike information criteria (AIC). RESULTS: 5,009 patients were divided into a TD (n 3339) and a VD (n 1670). In the TD, the model with the best performance (lowest AIC) was built with the following variables: Age, estrogen receptor status, tumor size, axillar adenopathy, AJCC anatomic clinical stage, Ki-67, and the Scarf-Bloom-Richardson score. This model had an AIC of 1241 and an AUC of 0.793 (95%CI 0.761 – 0.825) p <0.0001 in the TD. A 10-fold cross-validation showed good stability of the model. In the VD, the model had an AUC = 0.812 (IC95% 0.774 – 0.850) P < 0.0001 and an AIC = 644. Finally, we present with an online APP and an online calculator for its clinical use. CONCLUSION: In a retrospective cohort of women with breast cancer, a prediction model built with clinical and pathological variables at diagnosis displayed a robust performance to measure the individual odds of BM. The model is currently considered for external validation in other institutions and countries.
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spelling pubmed-104023932023-08-05 SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN Cacho-Díaz, Bernardo Reynoso-Noveron, Nancy Neurooncol Adv Final Category: Screening/Diagnostics/Prognostics BACKGROUND: Breast cancer (BC) is a leading cause of mortality and the most frequent malignancy in women; most deaths are due to metastatic disease, expressly brain metastases (BM). Currently, there is no biomarker or a prediction model to accurately predict BM. OBJECTIVE: To generate a BM prediction model from variables acquired at BC diagnosis. METHODS: A retrospective cohort of BC women diagnosed from 2009 to 2020 at a single center was divided into training (TD) and validation datasets (VD). The TD was used to generate a multivariable prediction model. The modeĹs performance was measured applying the area under the curve (AUC), C-statistic, and the Akaike information criteria (AIC). RESULTS: 5,009 patients were divided into a TD (n 3339) and a VD (n 1670). In the TD, the model with the best performance (lowest AIC) was built with the following variables: Age, estrogen receptor status, tumor size, axillar adenopathy, AJCC anatomic clinical stage, Ki-67, and the Scarf-Bloom-Richardson score. This model had an AIC of 1241 and an AUC of 0.793 (95%CI 0.761 – 0.825) p <0.0001 in the TD. A 10-fold cross-validation showed good stability of the model. In the VD, the model had an AUC = 0.812 (IC95% 0.774 – 0.850) P < 0.0001 and an AIC = 644. Finally, we present with an online APP and an online calculator for its clinical use. CONCLUSION: In a retrospective cohort of women with breast cancer, a prediction model built with clinical and pathological variables at diagnosis displayed a robust performance to measure the individual odds of BM. The model is currently considered for external validation in other institutions and countries. Oxford University Press 2023-08-04 /pmc/articles/PMC10402393/ http://dx.doi.org/10.1093/noajnl/vdad070.092 Text en © The Author(s) 2023. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Final Category: Screening/Diagnostics/Prognostics
Cacho-Díaz, Bernardo
Reynoso-Noveron, Nancy
SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title_full SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title_fullStr SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title_full_unstemmed SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title_short SDPS-38 A BRAIN METASTASES PREDICTION MODEL IN BREASTCANCER WOMEN
title_sort sdps-38 a brain metastases prediction model in breastcancer women
topic Final Category: Screening/Diagnostics/Prognostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402393/
http://dx.doi.org/10.1093/noajnl/vdad070.092
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