TY - JOUR
T1 - Accessible model predicts response in hormone receptor positive HER2 negative breast cancer receiving neoadjuvant chemotherapy
AU - Mastrantoni, Luca
AU - Garufi, Giovanna
AU - Giordano, Giulia
AU - Maliziola, Noemi
AU - Di Monte, Elena
AU - Arcuri, Giorgia
AU - Frescura, Valentina
AU - Rotondi, Angelachiara
AU - Orlandi, Armando
AU - Carbognin, Luisa
AU - Palazzo, Antonella
AU - Miglietta, Federica
AU - Pontolillo, Letizia
AU - Fabi, Alessandra
AU - Gerratana, Lorenzo
AU - Pannunzio, Sergio
AU - Paris, Ida
AU - Pilotto, Sara
AU - Marazzi, Fabio
AU - Franco, Antonio
AU - Franceschini, Gianluca
AU - Dieci, Maria Vittoria
AU - Mazzeo, Roberta
AU - Puglisi, Fabio
AU - Guarneri, Valentina
AU - Milella, Michele
AU - Scambia, Giovanni
AU - Giannarelli, Diana
AU - Tortora, Giampaolo
AU - Bria, Emilio
PY - 2025
Y1 - 2025
N2 - Hormone receptor-positive/HER2-negative breast cancer (BC) is the most common subtype of BC and typically occurs as an early, operable disease. In patients receiving neoadjuvant chemotherapy (NACT), pathological complete response (pCR) is rare and multiple efforts have been made to predict disease recurrence. We developed a framework to predict pCR using clinicopathological characteristics widely available at diagnosis. The machine learning (ML) models were trained to predict pCR (n = 463), evaluated in an internal validation cohort (n = 109) and validated in an external validation cohort (n = 151). The best model was an Elastic Net, which achieved an area under the curve (AUC) of respectively 0.86 and 0.81. Our results highlight how simpler models using few input variables can be as valuable as more complex ML architectures. Our model is freely available and can be used to enhance the stratification of BC patients receiving NACT, providing a framework for the development of risk-adapted clinical trials.
AB - Hormone receptor-positive/HER2-negative breast cancer (BC) is the most common subtype of BC and typically occurs as an early, operable disease. In patients receiving neoadjuvant chemotherapy (NACT), pathological complete response (pCR) is rare and multiple efforts have been made to predict disease recurrence. We developed a framework to predict pCR using clinicopathological characteristics widely available at diagnosis. The machine learning (ML) models were trained to predict pCR (n = 463), evaluated in an internal validation cohort (n = 109) and validated in an external validation cohort (n = 151). The best model was an Elastic Net, which achieved an area under the curve (AUC) of respectively 0.86 and 0.81. Our results highlight how simpler models using few input variables can be as valuable as more complex ML architectures. Our model is freely available and can be used to enhance the stratification of BC patients receiving NACT, providing a framework for the development of risk-adapted clinical trials.
KW - n/a
KW - n/a
UR - https://publicatt.unicatt.it/handle/10807/311559
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85218161336&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85218161336&origin=inward
U2 - 10.1038/s41523-025-00727-w
DO - 10.1038/s41523-025-00727-w
M3 - Article
SN - 2374-4677
VL - 11
SP - N/A-N/A
JO - npj Breast Cancer
JF - npj Breast Cancer
IS - 1
ER -