DNA mutational differences in cytological specimens from pancreatic cancer and cholangiocarcinoma

Pancreatology. 2010;10(4):429-33. doi: 10.1159/000318807. Epub 2010 Aug 19.

Abstract

Background/aims: Preoperative distinction between pancreatic cancer (PC) and extrahepatic cholangiocarcinoma (CC) is desirable due to diverging management options, and to optimize enrollment into neoadjuvant trials.

Methods: A single-center retrospective study of patients with PC or CC was undertaken. Four blinded pathologists reviewed all cases and reached a consensus diagnosis (PC or CC). Microdissection-based multiple microsatellite loss analysis and direct sequencing of K-ras oncogene was performed and compared for PC and CC.

Results: Of 33 cases studied (17 males; 16 PC, 17 CC; 10 with primary sclerosing cholangitis), a K-ras mutation was present in 14/16 (87.5%) PC and 1/17 (5.9%) CC cases (p < 0.001), sensitivity and specificity were 87.5 and 94%, respectively. The mean fractional mutational rate was higher in PC (0.51; 95% CI 0.45-0.58) compared to CC (0.34; 95% CI 0.28-0.39, p < 0.001).

Conclusions: The presence of a K-ras mutation in cytology specimens distinguishes PC from CC in this study. and IAP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Bile Duct Neoplasms / diagnosis
  • Bile Duct Neoplasms / genetics*
  • Bile Ducts, Intrahepatic / pathology*
  • Carcinoma, Pancreatic Ductal / diagnosis
  • Carcinoma, Pancreatic Ductal / genetics*
  • Cholangiocarcinoma / diagnosis
  • Cholangiocarcinoma / genetics*
  • Cholangitis, Sclerosing / genetics
  • Cholangitis, Sclerosing / pathology
  • DNA Mutational Analysis*
  • DNA, Neoplasm / analysis
  • Female
  • Genes, ras / genetics
  • Humans
  • Male
  • Microdissection
  • Microsatellite Instability
  • Middle Aged
  • Mutation
  • Pancreatic Neoplasms / diagnosis
  • Pancreatic Neoplasms / genetics*
  • Predictive Value of Tests
  • Retrospective Studies
  • Sensitivity and Specificity

Substances

  • DNA, Neoplasm