Abstract
Early detection remains an important opportunity to improve overall survival from pancreatic cancer but is challenging in the absence of an early disease biomarker. Therefore, screening patients at increased risk for pancreatic cancer is currently the favored strategy. This approach involves careful assessment of a patient’s family history and genetic profile as well as other nongenetic risk factors. Screening is typically offered to those with an exceptionally high cumulative risk for developing pancreatic cancer. There are several remaining knowledge gaps for which additional evidence to demonstrate effectiveness and guide clinical decisions is needed. In this chapter, we review the data supporting the role of screening for pancreatic cancer and discuss practical considerations for implementing this into clinical practice.
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Abbreviations
- CAPS:
-
Cancer of the Pancreas Screening Consortium
- DM:
-
Diabetes mellitus
- EUS:
-
Endoscopic ultrasound
- FDR:
-
First-degree relative
- FNA:
-
Fine needle aspiration
- FPC:
-
Familial pancreatic cancer
- PDAC:
-
Pancreatic ductal adenocarcinoma
- SDR:
-
Second-degree relative
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Hart, P.A., Stanich, P.P., Hampel, H. (2018). Screening for Pancreatic Cancer: Who to Screen and How to Follow-Up?. In: Bekaii-Saab, T., El-Rayes, B. (eds) Current and Emerging Therapies in Pancreatic Cancer . Springer, Cham. https://doi.org/10.1007/978-3-319-58256-6_4
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DOI: https://doi.org/10.1007/978-3-319-58256-6_4
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