KRAS mutation as a prognostic factor in ampullary adenocarcinoma: a meta-analysis and review

Oncotarget. 2016 Sep 6;7(36):58001-58006. doi: 10.18632/oncotarget.11156.

Abstract

Ampullary adenocarcinoma (A-AC) is a rare malignancy arising from the ampulla of Vater. KRAS mutation is detected in 30-40% of patients with A-AC, but its clinical implication and prognostic value are not well described. We conducted this meta-analysis to investigate the association between KRAS mutation and prognosis in patients with A-AC. We searched Pubmed, MEDLINE, EMBASE, and the Cochrane Library databases for articles including following terms in their titles, abstracts, or keywords: 'ampullary or periampullary or ampulla of vater', 'cancer or carcinoma', and 'KRAS'. There were five studies with survival data of patients. A total of 388 patients with A-AC from the 5 studies were included in the overall survival (OS) analysis, and 169 patients from 2 studies were eligible for the relapse-free-survival (RFS) analysis. Out of 388 patients, 175 (45%) had KRAS mutation. There was no association between KRAS mutation and OS (HR = 1.06, 95% CI: 0.87-1.29, P = 0.58). However, there was a significant correlation between KRAS mutation and worse RFS (HR = 2.74, 95% CI: 1.52-4.92, P = 0.0008). In conclusion, this meta-analysis indicates that KRAS mutation is associated with poor RFS, but not with OS in patients with A-AC.

Keywords: KRAS mutation; ampullary adenocarcinoma; meta-analysis; prognosis.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Adenocarcinoma / genetics*
  • Adenocarcinoma / mortality*
  • Ampulla of Vater
  • Biomarkers, Tumor / genetics
  • Disease-Free Survival
  • Humans
  • Mutation
  • Neoplasm Recurrence, Local / genetics
  • Neoplasm Recurrence, Local / mortality
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / mortality*
  • Prognosis
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Survival Analysis

Substances

  • Biomarkers, Tumor
  • KRAS protein, human
  • Proto-Oncogene Proteins p21(ras)