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Risk of early progression according to circulating ESR1 mutation, CA-15.3 and cfDNA increases under first-line anti-aromatase treatment in metastatic breast cancer.


ABSTRACT: BACKGROUND:Endocrine therapy is recommended as a first-line treatment for hormone receptor-positive metastatic breast cancer (HR+MBC) patients. No biomarker has been validated to predict tumor progression in that setting. We aimed to prospectively compare the risk of early progression according to circulating ESR1 mutations, CA-15.3, and circulating cell-free DNA in MBC patients treated with a first-line aromatase inhibitor (AI). METHODS:Patients with MBC treated with a first-line AI were prospectively included. Circulating biomarker assessment was performed every 3?months. The primary objective was to determine the risk of progression or death at the next follow-up visit (after 3?months) in case of circulating ESR1 mutation detection among patients treated with a first-line AI for HR+MBC. RESULTS:Overall, 103 patients were included, and 70 (68%) had progressive disease (PD). Circulating ESR1 mutations were detected in 22/70 patients with PD and in 0/33 patients without progression (p?

SUBMITTER: Clatot F 

PROVIDER: S-EPMC7254698 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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<h4>Background</h4>Endocrine therapy is recommended as a first-line treatment for hormone receptor-positive metastatic breast cancer (HR+MBC) patients. No biomarker has been validated to predict tumor progression in that setting. We aimed to prospectively compare the risk of early progression according to circulating ESR1 mutations, CA-15.3, and circulating cell-free DNA in MBC patients treated with a first-line aromatase inhibitor (AI).<h4>Methods</h4>Patients with MBC treated with a first-line  ...[more]

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