FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer

Abstract Biomarkers to identify patients without benefit from adding everolimus to endocrine treatment in metastatic breast cancer (MBC) are needed. We report the results of the Pearl trial conducted in five Belgian centers assessing 18F-FDG-PET/CT non-response (n = 45) and ctDNA detection (n = 46)...

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Autores principales: Andrea Gombos, David Venet, Lieveke Ameye, Peter Vuylsteke, Patrick Neven, Vincent Richard, Francois P. Duhoux, Jean-Francois Laes, Françoise Rothe, Christos Sotiriou, Marianne Paesmans, Ahmad Awada, Thomas Guiot, Patrick Flamen, Martine Piccart-Gebhart, Michail Ignatiadis, Géraldine Gebhart
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/0d02b04773dd46e4a2043969e5d6a963
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spelling oai:doaj.org-article:0d02b04773dd46e4a2043969e5d6a9632021-12-02T15:15:23ZFDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer10.1038/s41523-021-00331-82374-4677https://doaj.org/article/0d02b04773dd46e4a2043969e5d6a9632021-09-01T00:00:00Zhttps://doi.org/10.1038/s41523-021-00331-8https://doaj.org/toc/2374-4677Abstract Biomarkers to identify patients without benefit from adding everolimus to endocrine treatment in metastatic breast cancer (MBC) are needed. We report the results of the Pearl trial conducted in five Belgian centers assessing 18F-FDG-PET/CT non-response (n = 45) and ctDNA detection (n = 46) after 14 days of exemestane-everolimus (EXE-EVE) to identify MBC patients who will not benefit. The metabolic non-response rate was 66.6%. Median PFS in non-responding patients (using as cut-off 25% for SUVmax decrease) was 3.1 months compared to 6.0 months in those showing response (HR: 0.77, 95% CI: 0.40–1.50, p = 0.44). The difference was significant when using a “post-hoc” cut-off of 15% (PFS 2.2 months vs 6.4 months). ctDNA detection at D14 was associated with PFS: 2.1 months vs 5.0 months (HR-2.5, 95% CI: 1.3–5.0, p = 0.012). Detection of ctDNA and/or the absence of 18F-FDG-PET/CT response after 14 days of EXE-EVE identifies patients with a low probability of benefiting from treatment. Independent validation is needed.Andrea GombosDavid VenetLieveke AmeyePeter VuylstekePatrick NevenVincent RichardFrancois P. DuhouxJean-Francois LaesFrançoise RotheChristos SotiriouMarianne PaesmansAhmad AwadaThomas GuiotPatrick FlamenMartine Piccart-GebhartMichail IgnatiadisGéraldine GebhartNature PortfolioarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Breast Cancer, Vol 7, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Andrea Gombos
David Venet
Lieveke Ameye
Peter Vuylsteke
Patrick Neven
Vincent Richard
Francois P. Duhoux
Jean-Francois Laes
Françoise Rothe
Christos Sotiriou
Marianne Paesmans
Ahmad Awada
Thomas Guiot
Patrick Flamen
Martine Piccart-Gebhart
Michail Ignatiadis
Géraldine Gebhart
FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
description Abstract Biomarkers to identify patients without benefit from adding everolimus to endocrine treatment in metastatic breast cancer (MBC) are needed. We report the results of the Pearl trial conducted in five Belgian centers assessing 18F-FDG-PET/CT non-response (n = 45) and ctDNA detection (n = 46) after 14 days of exemestane-everolimus (EXE-EVE) to identify MBC patients who will not benefit. The metabolic non-response rate was 66.6%. Median PFS in non-responding patients (using as cut-off 25% for SUVmax decrease) was 3.1 months compared to 6.0 months in those showing response (HR: 0.77, 95% CI: 0.40–1.50, p = 0.44). The difference was significant when using a “post-hoc” cut-off of 15% (PFS 2.2 months vs 6.4 months). ctDNA detection at D14 was associated with PFS: 2.1 months vs 5.0 months (HR-2.5, 95% CI: 1.3–5.0, p = 0.012). Detection of ctDNA and/or the absence of 18F-FDG-PET/CT response after 14 days of EXE-EVE identifies patients with a low probability of benefiting from treatment. Independent validation is needed.
format article
author Andrea Gombos
David Venet
Lieveke Ameye
Peter Vuylsteke
Patrick Neven
Vincent Richard
Francois P. Duhoux
Jean-Francois Laes
Françoise Rothe
Christos Sotiriou
Marianne Paesmans
Ahmad Awada
Thomas Guiot
Patrick Flamen
Martine Piccart-Gebhart
Michail Ignatiadis
Géraldine Gebhart
author_facet Andrea Gombos
David Venet
Lieveke Ameye
Peter Vuylsteke
Patrick Neven
Vincent Richard
Francois P. Duhoux
Jean-Francois Laes
Françoise Rothe
Christos Sotiriou
Marianne Paesmans
Ahmad Awada
Thomas Guiot
Patrick Flamen
Martine Piccart-Gebhart
Michail Ignatiadis
Géraldine Gebhart
author_sort Andrea Gombos
title FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
title_short FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
title_full FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
title_fullStr FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
title_full_unstemmed FDG positron emission tomography imaging and ctDNA detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
title_sort fdg positron emission tomography imaging and ctdna detection as an early dynamic biomarker of everolimus efficacy in advanced luminal breast cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0d02b04773dd46e4a2043969e5d6a963
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