| Literature DB >> 31679210 |
Asad Ur Rahman1, Effa Zahid2, Muhammad Talha Khan3, Awais Naeem4, Saeed Ali5, Mamoon Ur Rashid6, Sarfraz Ahmad7.
Abstract
Up to 20% of patients with pancreatic cancer have a family history of the disease. Familial pancreatic cancer is defined as at least two first-degree relatives with pancreatic cancer that occurs without being part of a cancer syndrome. Although this does not follow a specific Mendelian pattern of inheritance, research is underway to better understand this cohort of patients. Recent expert opinion/recommendations encourage physicians treating patients with pancreatic cancer to ask them to consider having germline testing. Herein, we summarize the current peer-reviewed literature on the most common syndromes associated with pancreatic cancer, associated genetic mutations, and recommendations from various consortia regarding screening strategies. Lastly, we describe the economic impact of pancreatic cancer and the impact of screening tools in high-risk populations.Entities:
Mesh:
Year: 2019 PMID: 31679210 DOI: 10.1615/CritRevOncog.2019031637
Source DB: PubMed Journal: Crit Rev Oncog ISSN: 0893-9675