Publications for Healthcare Professionals

Publications for Healthcare Professionals

Stay up to date with ClearNote Health and be among the first to learn about our latest advances with the Avantect test. Bookmark this section for updates, news releases, publications, and more.

Clinical publications

Based on more than 50,000 assays in over 14,000 samples across 150+ sites, we have more than 25 scientific publications and presentations.

September 2024

Analytical Validation of an Early Detection Pancreatic Cancer Test Using 5-Hydroxymethylation Signatures

The Journal of Molecular Diagnostics

October 2020

Detection of early stage pancreatic cancer using 5-hydroxymethylcytosine signatures in circulating cell free DNA

Nature Communications

September 2018

Detection of early stage pancreatic cancer using 5-hydroxymethylcytosine signatures in circulating cell free DNA

bioRxiv

March 2023

Epigenomic Blood-Based Early Detection of Pancreatic Cancer Employing Cell-Free DNA


Clinical Gastroenterology and Hepatology

January 2020

Pilot study demonstrating changes in DNA hydroxymethylation enable detection of multiple cancers in plasma cell-free DNA

medRxiv

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For patients at high risk, the Avantect test could make a
life-changing difference.

Important information

The Avantect Pancreatic Cancer Test is an early detection test. The test does not establish a diagnosis of pancreatic cancer, and results should be considered in the context of other clinical criteria. Definitive diagnosis of pancreatic cancer usually requires a series of imaging scans, blood tests, and a biopsy. Not all pancreatic cancers will be detected. Some patients with pancreatic cancer may have a “Signal not detected” result. Some patients without pancreatic cancer may have a “Signal detected” result. False-negative and false-positive results are possible. A “Signal not detected” result does not guarantee that no pancreatic cancer is present. In some cases, no result is obtained. While this is very uncommon, it may be caused by shipping delays or when there is not enough cell-free DNA for the test in the patient’s blood. If this happens, we generally ask for a repeat blood sample for testing at no extra cost.

The test was developed in the ClearNote Health CLIA-certified (CLIA# 05D2249973) and CAP-accredited (CAP# 9219174) laboratory and has not been cleared or approved by the US Food and Drug Administration (FDA).