Personalized recurrence risk prediction in early-stage breast cancer through an integrative mathematical model based on MammaPrint®, radiotherapy, phenotype, and clinicopathological factors

The predictive model fitted using Firth's penalized logistic regression demonstrated an adequate discriminative ability (AUC = 0.755). MMP was the variable with the greatest weight, followed by RT. These variables allow for a more accurate prediction of recurrence risk than traditional clinicopathological factors, supporting their value in the personalization of treatment. This study reports statistically significant differences when comparing the group without radiotherapy (BED = 0 Gy) to the low-dose group (BED < 60 Gy), with a p-value of 0.0475.

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Publication Details

Journal
Clinical & Translational Oncology
Published
2025-10-03
DOI
https://doi.org/10.1007/s12094-025-04065-y
Primary Topic
Breast Cancer Treatment Studies
Type
article
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article

Personalized recurrence risk prediction in early-stage breast cancer through an integrative mathematical model based on MammaPrint®, radiotherapy, phenotype, and clinicopathological factors

José Manuel López Vega, Ana de Juan Ferré, J. Sánchez Mazón, Carlos López
Clinical & Translational Oncology
Breast Cancer Treatment Studies
article

Personalized recurrence risk prediction in early-stage breast cancer through an integrative mathematical model based on MammaPrint®, radiotherapy, phenotype, and clinicopathological factors

José Manuel López Vega, Ana de Juan Ferré, J. Sánchez Mazón, Carlos López
article en

Abstract

The predictive model fitted using Firth's penalized logistic regression demonstrated an adequate discriminative ability (AUC = 0.755). MMP was the variable with the greatest weight, followed by RT. These variables allow for a more accurate prediction of recurrence risk than traditional clinicopathological factors, supporting their value in the personalization of treatment. This study reports statistically significant differences when comparing the group without radiotherapy (BED = 0 Gy) to the low-dose group (BED < 60 Gy), with a p-value of 0.0475.

Clinical & Translational OncologyVol. 28(3)
Universidad de Cantabria (ES), Marqués de Valdecilla University Hospital (ES)
Openalex Percentile: Top 66%
Breast Cancer Treatment Studies
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