Advancements in non-invasive biomarkers for detection and monitoring of breast cancer recurrence
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Date
2025
Journal Title
Journal ISSN
Volume Title
Publisher
SCIENCE PROGRESS
Abstract
Breast cancer recurrence remains a major cause of mortality, with up to 30% of early
stage patients relapsing as incurable metastatic disease. Conventional surveillance with
imaging and serum markers (CA15–3, CEA) lacks the sensitivity and specificity to detect
minimal residual disease. This narrative review examines non-invasive biomarkers such
as circulating tumor DNA (ctDNA), circulating tumor cells (CTCs) and exosomes and
the technologies enhancing their performance. Droplet digital PCR and next-generation
sequencing detect ctDNA at allele frequencies below 0.1%, identifying molecular relapse
a median of 10–12 months before radiologic progression. Microfluidic and affinity-based
platforms isolate CTCs with over 75% sensitivity in metastatic settings. Nanoengineered
sensors and standardized workflows improve exosome isolation, revealing miRNA and
protein signatures predictive of recurrence. Proteomic and metabolomic profiling iden
tify dysregulated metabolic pathways and protein networks, offering functional insights
that complement molecular assays. Integrative multi-omics approaches merge genomic,
transcriptomic, proteomic and metabolomic data; machine-learning frameworks detect
subtle patterns and correlations, enabling dynamic, personalized surveillance. By detect
ing molecular and functional biomarkers early, clinicians can tailor therapy, monitor
treatment response and intervene promptly. Challenges include low analyte abundance,
assay variability, high costs and lack of standardized protocols, limiting clinical adoption.
Prospective validation in large cohorts is critical. We highlight ongoing clinical trials such
as ctDNA-guided adjuvant therapy and CTC-driven stratification studies that aim to
establish clinical utility. Non-invasive biomarker platforms could shift breast cancer fol
low-up from reactive detection to proactive intervention, ultimately improving survival
and quality of life through personalized, real-time monitoring.
Description
Keywords
Breast cancer recurrence, liquid biopsy, circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), exosomes
