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Personalized circulating tumor DNA testing for detection of progression and treatment response monitoring in patients with metastatic invasi

Personalized circulating tumor DNA testing for detection of progression and treatment response monitoring in patients with metastatic invasi

Published Date January 2, 2024

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Circulating tumor DNA (ctDNA) monitoring of estrogen receptor-positive, human epidermal growth factor receptor 2-negative (ER+/HER2-) high r
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Personalized circulating tumor DNA monitoring to predict response to neoadjuvant therapy in patients with early-stage breast cancer

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The tests described have been developed and their performance characteristics determined by the CLIA-certified laboratory performing the test. The tests have not been cleared or approved by the US Food and Drug Administration (FDA). CAP accredited, ISO 13485 certified, and CLIA certified. © 2024 Natera, Inc. All Rights Reserved.