Prognostic value of circulating cell-free DNA in patients with pancreatic cancer: A systemic review and meta-analysis

Gene. 2018 Dec 30:679:328-334. doi: 10.1016/j.gene.2018.09.029. Epub 2018 Sep 15.

Abstract

Because of the deep research about tumorigenesis mechanism, the cognition of cancer has been transferred to molecular level from morphology. Previous articles reported a potential connection between circulating cell-free DNA (cfDNA) and prognosis of pancreatic cancer. A total of 18 related articles including 1243 patients were enrolled to access the relationship between cfDNA and prognosis of pancreatic cancer. The hazard ratio (HR) was used to combine the univariate and multivariate results of included studies. Our result performed that the cfDNA had significant prognostic value in predicting OS (HR = 2.41, 95%CI: 1.93-3.02, I2 = 60%) and PFS (HR = 2.47, 95%CI: 1.80-3.40, I2 = 0%) in univariate analysis. The multivariate analyses about OS (HR = 2.57, 95%CI: 1.95-3.38, I2 = 66%) and PFS (HR = 2.31, 95%CI: 1.47-3.64, I2 = 0%) also showed significance. In conclusion, the cfDNA was a significant prognostic factor for OS and PFS in patients with pancreatic cancer. The mutation (Kras, ERBB2-exon17 and KrasG12V), circulating tumor DNA (ctDNA) presence, hypermethylation and higher concentration of cfDNA were both associated with worse survival results in pancreatic cancer.

Keywords: Circulating cell-free DNA; Meta-analysis; Pancreatic cancer; Prognosis.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Cell-Free Nucleic Acids / genetics*
  • Circulating Tumor DNA / genetics
  • DNA Methylation
  • Exons
  • Female
  • Humans
  • Male
  • Mutation*
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / pathology
  • Prognosis
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Receptor, ErbB-2 / genetics*
  • Survival Analysis

Substances

  • Cell-Free Nucleic Acids
  • Circulating Tumor DNA
  • KRAS protein, human
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Proto-Oncogene Proteins p21(ras)