» Articles » PMID: 39684756

Molecular Profiling of Endocrine Resistance in HR+/HER2-Metastatic Breast Cancer: Insights from Extracellular Vesicles-Derived DNA and CtDNA in Liquid Biopsies

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Dec 17
PMID 39684756
Authors
Affiliations
Soon will be listed here.
Abstract

Standard treatments in hormone receptor-positive (HR+)/HER2-metastatic breast cancer (mBC) typically involve endocrine therapy (ET) combined with CDK4/6 inhibitors, yet resistance to ET remains a persistent challenge in advanced cases. A deeper knowledge of the use of liquid biopsy is crucial for the implementation of precision medicine in mBC with real-time treatment guidance. Our study assesses the prognostic value of and mutations in DNA derived from extracellular vesicles (EV-DNA) in longitudinal plasma from 59 HR+/HER2-mBC patients previously exposed to aromatase inhibitors, with a comparative analysis against circulating tumor DNA (ctDNA). Mutations were evaluated by digital PCR. and mutations were found in 22 and 25% of patients. Baseline mutations in EV-DNA were associated with shorter progression-free survival (PFS) across the cohort, with the Y537S mutation showing a particularly strong impact on the outcome of fulvestrant-treated patients. In contrast, mutations in EV-DNA did not significantly correlate with PFS, whereas in ctDNA, they were linked to poor outcomes. Altogether, this study positions EV-DNA as a valuable biomarker alongside ctDNA, enriching the understanding of different analytes in liquid biopsy and supporting strategies for HR+/HER2-mBC in precision oncology.

References
1.
Ignatiadis M, Rack B, Rothe F, Riethdorf S, Decraene C, Bonnefoi H . Liquid biopsy-based clinical research in early breast cancer: The EORTC 90091-10093 Treat CTC trial. Eur J Cancer. 2016; 63:97-104. DOI: 10.1016/j.ejca.2016.04.024. View

2.
Bidard F, Hardy-Bessard A, Dalenc F, Bachelot T, Pierga J, de La Motte Rouge T . Switch to fulvestrant and palbociclib versus no switch in advanced breast cancer with rising ESR1 mutation during aromatase inhibitor and palbociclib therapy (PADA-1): a randomised, open-label, multicentre, phase 3 trial. Lancet Oncol. 2022; 23(11):1367-1377. DOI: 10.1016/S1470-2045(22)00555-1. View

3.
Sparano J, ONeill A, Alpaugh K, Wolff A, Northfelt D, Dang C . Association of Circulating Tumor Cells With Late Recurrence of Estrogen Receptor-Positive Breast Cancer: A Secondary Analysis of a Randomized Clinical Trial. JAMA Oncol. 2018; 4(12):1700-1706. PMC: 6385891. DOI: 10.1001/jamaoncol.2018.2574. View

4.
Will M, Liang J, Metcalfe C, Chandarlapaty S . Therapeutic resistance to anti-oestrogen therapy in breast cancer. Nat Rev Cancer. 2023; 23(10):673-685. PMC: 10529099. DOI: 10.1038/s41568-023-00604-3. View

5.
Aftimos P, Oliveira M, Irrthum A, Fumagalli D, Sotiriou C, Nili Gal-Yam E . Genomic and Transcriptomic Analyses of Breast Cancer Primaries and Matched Metastases in AURORA, the Breast International Group (BIG) Molecular Screening Initiative. Cancer Discov. 2021; 11(11):2796-2811. PMC: 9414283. DOI: 10.1158/2159-8290.CD-20-1647. View