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ctDNA monitoring to optimize immunotherapy treatment decisions

ctDNA monitoring to optimize immunotherapy treatment decisions

Published Date September 22, 2023

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Signatera Patient Discussion Guide
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Circulating tumor DNA (ctDNA) dynamics and survival outcomes in patients with advanced NSCLC and high (≥50%) PD-L1 expression

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Feasibility of Longitudinal ctDNA Assessment in Patients with Uterine and Extra-Uterine Leiomyosarcoma

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Early Relapse Detection and Monitoring Disease Status in Patients with Early-stage Pancreatic Adenocarcinoma using Circulating Tumor DNA

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Practical recommendations for using ctDNA in clinical decision making

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Case report: Real-world experience using a personalized cancer-specific circulating tumor DNA assay in different metastatic melanoma scenari

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Feasibility of Personalized ctDNA Detection in Stage II and III Melanoma

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Neoadjuvant Durvalumab Alone or Combined with Novel Immuno-Oncology Agents in Resectable Lung Cancer: The Phase 2 NeoCOAST Platform Trial

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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). Although FDA is exercising enforcement discretion of premarket review and other regulations for laboratory-developed tests in the US, certification of the laboratory is required under CLIA to ensure the quality and validity of the tests. CAP accredited, ISO 13485 certified, and CLIA certified. © 2023 Natera, Inc. All Rights Reserved.