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Oncology
Treatment Monitoring Utilizing ctDNA-based Molecular Residual Disease Detection in Early Stage Uterine Cancer

Treatment Monitoring Utilizing ctDNA-based Molecular Residual Disease Detection in Early Stage Uterine Cancer

Published Date March 20, 2024

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PARPi response monitoring using personalized circulating tumor DNA testing in patients with ovarian cancer
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Utility of ctDNA as an Early Predictive Biomarker of Response to RT/CRT in Gynecologic Malignancies

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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.