4.6 Review

Role of ctDNA in Breast Cancer

Journal

CANCERS
Volume 14, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cancers14020310

Keywords

ctDNA; breast cancer; personalized medicine; liquid biopsy; cancer diagnosis

Categories

Funding

  1. Instituto de Salud Carlos III [ISCIII CM20/00027]

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Circulating tumor DNA (ctDNA) plays an important role in breast cancer research and clinical practice, allowing for screening, diagnosis, treatment selection, and prognosis assessment. Analysis of ctDNA provides a more accurate understanding of the heterogeneity of breast cancer, enabling monitoring of disease progression and resistance mutations. With the application of new bioinformatics tools, the use of ctDNA in breast cancer will become more frequent, enhancing our knowledge of tumor biology.
Simple Summary Circulating tumor DNA is DNA released by the tumor into the bloodstream. In breast cancer, it is used mainly in research or in clinical trials, but it will likely be used in routine clinical practice once certain issues have been worked out and methods of analysis have been improved and standardized. Breast cancer classification and treatment selection are now based on analysis of the tumor but circulating tumor DNA carries many features of the original tumor and can be analyzed from a simple, non-invasive blood extraction. Here, we review its potential role in early breast cancer (for screening, diagnosis, detection of minimal residual disease after surgery, follow up, and treatment) and in metastatic breast cancer (for the detection of mutations, prognosis and treatment). Breast cancer is currently classified by immunohistochemistry. However, technological advances in the detection of circulating tumor DNA (ctDNA) have made new options available for diagnosis, classification, biological knowledge, and treatment selection. Breast cancer is a heterogeneous disease and ctDNA can accurately reflect this heterogeneity, allowing us to detect, monitor, and understand the evolution of the disease. Breast cancer patients have higher levels of circulating DNA than healthy subjects, and ctDNA can be used for different objectives at different timepoints of the disease, ranging from screening and early detection to monitoring for resistance mutations in advanced disease. In early breast cancer, ctDNA clearance has been associated with higher rates of complete pathological response after neoadjuvant treatment and with fewer recurrences after radical treatments. In metastatic disease, ctDNA can help select the optimal sequencing of treatments. In the future, thanks to new bioinformatics tools, the use of ctDNA in breast cancer will become more frequent, enhancing our knowledge of the biology of tumors. Moreover, deep learning algorithms may also be able to predict breast cancer evolution or treatment sensitivity. In the coming years, continued research and the improvement of liquid biopsy techniques will be key to the implementation of ctDNA analysis in routine clinical practice.

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