| Literature DB >> 27672215 |
Babs G Sibinga Mulder1, J Sven D Mieog1, Henricus J M Handgraaf1, Arantza Farina Sarasqueta2, Hans F A Vasen3, Thomas P Potjer4, Rutger-Jan Swijnenburg1, Saskia A C Luelmo5, Shirin Feshtali6, Akin Inderson3, Alexander L Vahrmeijer1, Bert A Bonsing1, Tom van Wezel2, Hans Morreau2.
Abstract
To improve the diagnostic value of fine-needle aspiration (FNA)-derived material, we perform targeted next-generation sequencing (NGS) in patients with a suspect lesion of the pancreas. The NGS analysis can lead to a change in the treatment plan or supports inconclusive or uncertain cytology results. We describe the advantages of NGS using one particular patient with a recurrent pancreatic lesion 7 years after resection of a pancreatic ductal adenocarcinoma (PDAC). Our NGS analysis revealed the presence of a presumed second primary cancer in the pancreatic remnant, which led to a change in treatment: resection with curative intend instead of palliation. Additionally, NGS identified an unexpected germline CDKN2A 19-base pair deletion, which predisposed the patient to developing PDAC. Preoperative NGS analysis of FNA-derived DNA can help identify patients at risk for developing PDAC and define future therapeutic options. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.Entities:
Keywords: CANCER; DIAGNOSTICS; DNA; MOLECULAR PATHOLOGY; PANCREAS
Mesh:
Substances:
Year: 2016 PMID: 27672215 DOI: 10.1136/jclinpath-2016-203928
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411