Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer

Abstract We aimed to study the incidence and genomic spectrum of actionable alterations (AA) detected in serial cfDNA collections from patients with metastatic breast cancer (MBC). Patients with MBC who underwent plasma-based cfDNA testing (Guardant360®) between 2015 and 2021 at an academic institut...

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Main Authors: Yael Bar, Jennifer C. Keenan, Andrzej Niemierko, Arielle J. Medford, Steven J. Isakoff, Leif W. Ellisen, Aditya Bardia, Neelima Vidula
Format: Article
Language:English
Published: Nature Portfolio 2024-04-01
Series:npj Breast Cancer
Online Access:https://doi.org/10.1038/s41523-024-00633-7
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author Yael Bar
Jennifer C. Keenan
Andrzej Niemierko
Arielle J. Medford
Steven J. Isakoff
Leif W. Ellisen
Aditya Bardia
Neelima Vidula
author_facet Yael Bar
Jennifer C. Keenan
Andrzej Niemierko
Arielle J. Medford
Steven J. Isakoff
Leif W. Ellisen
Aditya Bardia
Neelima Vidula
author_sort Yael Bar
collection DOAJ
description Abstract We aimed to study the incidence and genomic spectrum of actionable alterations (AA) detected in serial cfDNA collections from patients with metastatic breast cancer (MBC). Patients with MBC who underwent plasma-based cfDNA testing (Guardant360®) between 2015 and 2021 at an academic institution were included. For patients with serial draws, new pathogenic alterations in each draw were classified as actionable alterations (AA) if they met ESCAT I or II criteria of the ESMO Scale for Clinical Actionability of Molecular Targets (ESCAT). A total of 344 patients with hormone receptor-positive (HR+)/HER2-negative (HER2-) MBC, 95 patients with triple-negative (TN) MBC and 42 patients with HER2-positive (HER2 + ) MBC had a baseline (BL) cfDNA draw. Of these, 139 HR+/HER2-, 33 TN and 13 HER2+ patients underwent subsequent cfDNA draws. In the HR+/HER2- cohort, the proportion of patients with new AA decreased from 63% at BL to 27–33% in the 2nd-4th draws (p < 0.0001). While some of the new AA in subsequent draws from patients with HR+/HER2- MBC were new actionable variants in the same genes that were known to be altered in previous draws, 10-24% of patients had new AA in previously unaltered genes. The incidence of new AA also decreased with subsequent draws in the TN and HER2+ cohorts (TN: 25% to 0–9%, HER2 + : 38% to 14–15%). While the incidence of new AA in serial cfDNA decreased with subsequent draws across all MBC subtypes, new alterations with a potential impact on treatment selection continued to emerge, particularly for patients with HR+/HER2- MBC.
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spelling doaj.art-9aff4fde10a345d2948de953d4a4b9752024-04-14T11:23:35ZengNature Portfolionpj Breast Cancer2374-46772024-04-0110111010.1038/s41523-024-00633-7Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancerYael Bar0Jennifer C. Keenan1Andrzej Niemierko2Arielle J. Medford3Steven J. Isakoff4Leif W. Ellisen5Aditya Bardia6Neelima Vidula7Massachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterMassachusetts General Hospital Cancer CenterAbstract We aimed to study the incidence and genomic spectrum of actionable alterations (AA) detected in serial cfDNA collections from patients with metastatic breast cancer (MBC). Patients with MBC who underwent plasma-based cfDNA testing (Guardant360®) between 2015 and 2021 at an academic institution were included. For patients with serial draws, new pathogenic alterations in each draw were classified as actionable alterations (AA) if they met ESCAT I or II criteria of the ESMO Scale for Clinical Actionability of Molecular Targets (ESCAT). A total of 344 patients with hormone receptor-positive (HR+)/HER2-negative (HER2-) MBC, 95 patients with triple-negative (TN) MBC and 42 patients with HER2-positive (HER2 + ) MBC had a baseline (BL) cfDNA draw. Of these, 139 HR+/HER2-, 33 TN and 13 HER2+ patients underwent subsequent cfDNA draws. In the HR+/HER2- cohort, the proportion of patients with new AA decreased from 63% at BL to 27–33% in the 2nd-4th draws (p < 0.0001). While some of the new AA in subsequent draws from patients with HR+/HER2- MBC were new actionable variants in the same genes that were known to be altered in previous draws, 10-24% of patients had new AA in previously unaltered genes. The incidence of new AA also decreased with subsequent draws in the TN and HER2+ cohorts (TN: 25% to 0–9%, HER2 + : 38% to 14–15%). While the incidence of new AA in serial cfDNA decreased with subsequent draws across all MBC subtypes, new alterations with a potential impact on treatment selection continued to emerge, particularly for patients with HR+/HER2- MBC.https://doi.org/10.1038/s41523-024-00633-7
spellingShingle Yael Bar
Jennifer C. Keenan
Andrzej Niemierko
Arielle J. Medford
Steven J. Isakoff
Leif W. Ellisen
Aditya Bardia
Neelima Vidula
Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
npj Breast Cancer
title Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
title_full Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
title_fullStr Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
title_full_unstemmed Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
title_short Genomic spectrum of actionable alterations in serial cell free DNA (cfDNA) analysis of patients with metastatic breast cancer
title_sort genomic spectrum of actionable alterations in serial cell free dna cfdna analysis of patients with metastatic breast cancer
url https://doi.org/10.1038/s41523-024-00633-7
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