TY - JOUR
T1 - Optimizing therapeutic approaches for HR+/HER2-advanced breast cancer
T2 - clinical perspectives on biomarkers and treatment strategies post-CDK4/6 inhibitor progression
AU - Andújar, Juan Miguel Cejalvo
AU - de la Peñ, Francisco Ayala
AU - Vila, Mireia Margeli
AU - Pascual, Javier
AU - Tolosa, Pablo
AU - Pages, Cristina
AU - Cuenca, Mónica
AU - Zotano, Ángel Guerrero
N1 - © The Author(s) 2025.
PY - 2025/1/21
Y1 - 2025/1/21
N2 - This review offers an expert perspective on biomarkers, CDK4/6 inhibitor efficacy, and therapeutic approaches for managing hormone receptor-positive (HR+), human epidermal growth factor receptor-negative (HER2-) advanced breast cancer (ABC), particularly after CDK4/6 inhibitor progression. Key trials have demonstrated that combining CDK4/6 inhibitors with endocrine therapy (ET) significantly improves progression-free survival (PFS), with median durations ranging from 14.8 to 26.7 months, and overall survival (OS), with median durations reaching up to 53.7 months. Actionable biomarkers, such as PIK3CA and ESR1 mutations, have emerged as pivotal tools to guide second-line treatment decisions, enabling the use of targeted therapies like alpelisib and elacestrant and emphasizing the important role of biomarkers in guiding the selection of therapy. This overview aims to provide clinicians with a practical and up-to-date framework to inform treatment decisions and improve patient care in the context of this challenging disease. Additionally, we review emerging biomarkers and novel treatment strategies to address this difficult clinical landscape.
AB - This review offers an expert perspective on biomarkers, CDK4/6 inhibitor efficacy, and therapeutic approaches for managing hormone receptor-positive (HR+), human epidermal growth factor receptor-negative (HER2-) advanced breast cancer (ABC), particularly after CDK4/6 inhibitor progression. Key trials have demonstrated that combining CDK4/6 inhibitors with endocrine therapy (ET) significantly improves progression-free survival (PFS), with median durations ranging from 14.8 to 26.7 months, and overall survival (OS), with median durations reaching up to 53.7 months. Actionable biomarkers, such as PIK3CA and ESR1 mutations, have emerged as pivotal tools to guide second-line treatment decisions, enabling the use of targeted therapies like alpelisib and elacestrant and emphasizing the important role of biomarkers in guiding the selection of therapy. This overview aims to provide clinicians with a practical and up-to-date framework to inform treatment decisions and improve patient care in the context of this challenging disease. Additionally, we review emerging biomarkers and novel treatment strategies to address this difficult clinical landscape.
KW - Advanced breast cancer
KW - Biomarkers
KW - HR+/HER2- CDK4/6 inhibitors
KW - Prognosis
KW - CDK4/6 inhibitors
KW - HR+/HER2-
KW - advanced breast cancer
KW - biomarkers
KW - prognosis
UR - https://www.scopus.com/pages/publications/105004406839
UR - https://www.mendeley.com/catalogue/0493ee20-cdd4-3b91-bf93-8b39bbcd5a73/
UR - https://portalrecerca.uab.cat/en/publications/b03552d4-00f0-408f-9f61-b0d9b7e3c686
U2 - 10.20517/cdr.2024.169
DO - 10.20517/cdr.2024.169
M3 - Review article
C2 - 39935426
AN - SCOPUS:105004406839
SN - 2578-532X
VL - 8
JO - Cancer Drug Resistance
JF - Cancer Drug Resistance
M1 - 5
ER -