The impact of a silent killer
In pancreatic cancer, the vast majority of patients are not diagnosed until their cancer has advanced and they have regional (stage III) or distant (stage IV) tumors.3 For these patients, the prognosis is poor.


~62,210 adults diagnosed in 20223
~49,830 deaths in the US in 20223
In pancreatic cancer, the vast majority of patients are not diagnosed until their cancer has advanced and they have regional (stage III) or distant (stage IV) tumors.3 For these patients, the prognosis is poor.
The stage of pancreatic cancer at diagnosis has a significant impact on survival.2 Pancreatic cancer diagnosed at its earliest stage (IA) can have a 5-year survival rate of over 80%.4
According to guidelines from the American Gastroenterological Association, pancreatic cancer screening in high-risk individuals should begin at age 50, or 10 years younger than the initial age of familial onset.8
Recent studies of the pathogenesis of pancreatic cancer suggest that although longstanding diabetes (>3 years) increases risk and may play a causal role, new-onset diabetes actually may be a consequence of pancreatic cancer.12
See how Avantect is changing the way pancreatic cancer is detected.
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).