Cell-free DNA (cfDNA) extracted from peripheral blood has emerged as a crucial biomarker source in oncology research. To enhance the detection of somatic copy number alterations (SCNAs) and circulating tumor DNA (ctDNA), we developed eSENSES, a 2 Mb breast cancer-targeted NGS panel. It includes 15,000 genome-wide SNPs, 500 focal SNPs in breast cancer driver regions, and exons from 81 commonly altered genes, alongside a custom computational approach. We assessed the performance of eSENSES using both synthetic and clinical samples showing that eSENSES can detect ctDNA levels below 1%, exhibiting high sensitivity and specificity at 2-3% ctDNA levels. In patients with metastatic breast cancer, ctDNA estimations correlated with disease progression. When compared with other technologies and state-of-the-art approaches, eSENSES demonstrated enhanced performance. eSENSES provides a reliable, powerful and cost-effective tool for monitoring disease progression and guiding therapeutic decisions i...

Cell-free DNA (cfDNA) extracted from peripheral blood has emerged as a crucial biomarker source in oncology research. To enhance the detection of somatic copy number alterations (SCNAs) and circulating tumor DNA (ctDNA), we developed eSENSES, a 2 Mb breast cancer-targeted NGS panel. It includes 15,000 genome-wide SNPs, 500 focal SNPs in breast cancer driver regions, and exons from 81 commonly altered genes, alongside a custom computational approach. We assessed the performance of eSENSES using both synthetic and clinical samples showing that eSENSES can detect ctDNA levels below 1%, exhibiting high sensitivity and specificity at 2-3% ctDNA levels. In patients with metastatic breast cancer, ctDNA estimations correlated with disease progression. When compared with other technologies and state-of-the-art approaches, eSENSES demonstrated enhanced performance. eSENSES provides a reliable, powerful and cost-effective tool for monitoring disease progression and guiding therapeutic decisions in breast cancer patients.

Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer / Scandino, Riccardo; Nardone, Agostina; Casiraghi, Nicola; Galardi, Francesca; Genovese, Mattia; Romagnoli, Dario; Paoli, Marta; Biagioni, Chiara; Tonina, Andrea; Migliaccio, Ilenia; Pestrin, Marta; Moretti, Erica; Malorni, Luca; Biganzoli, Laura; Benelli, Matteo; Romanel, Alessandro. - In: NPJ BREAST CANCER. - ISSN 2374-4677. - 11:1(2025), pp. 2501-2512. [10.1038/s41523-025-00739-6]

Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer

Scandino, Riccardo;Casiraghi, Nicola;Romagnoli, Dario;Paoli, Marta;Benelli, Matteo;Romanel, Alessandro
2025-01-01

Abstract

Cell-free DNA (cfDNA) extracted from peripheral blood has emerged as a crucial biomarker source in oncology research. To enhance the detection of somatic copy number alterations (SCNAs) and circulating tumor DNA (ctDNA), we developed eSENSES, a 2 Mb breast cancer-targeted NGS panel. It includes 15,000 genome-wide SNPs, 500 focal SNPs in breast cancer driver regions, and exons from 81 commonly altered genes, alongside a custom computational approach. We assessed the performance of eSENSES using both synthetic and clinical samples showing that eSENSES can detect ctDNA levels below 1%, exhibiting high sensitivity and specificity at 2-3% ctDNA levels. In patients with metastatic breast cancer, ctDNA estimations correlated with disease progression. When compared with other technologies and state-of-the-art approaches, eSENSES demonstrated enhanced performance. eSENSES provides a reliable, powerful and cost-effective tool for monitoring disease progression and guiding therapeutic decisions i...
2025
1
Scandino, Riccardo; Nardone, Agostina; Casiraghi, Nicola; Galardi, Francesca; Genovese, Mattia; Romagnoli, Dario; Paoli, Marta; Biagioni, Chiara; Toni...espandi
Enabling sensitive and precise detection of ctDNA through somatic copy number aberrations in breast cancer / Scandino, Riccardo; Nardone, Agostina; Casiraghi, Nicola; Galardi, Francesca; Genovese, Mattia; Romagnoli, Dario; Paoli, Marta; Biagioni, Chiara; Tonina, Andrea; Migliaccio, Ilenia; Pestrin, Marta; Moretti, Erica; Malorni, Luca; Biganzoli, Laura; Benelli, Matteo; Romanel, Alessandro. - In: NPJ BREAST CANCER. - ISSN 2374-4677. - 11:1(2025), pp. 2501-2512. [10.1038/s41523-025-00739-6]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/451770
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