Correlation between EGFR mutations and serum tumor markers in lung adenocarcinoma patients

Asian Pac J Cancer Prev. 2013;14(2):695-700. doi: 10.7314/apjcp.2013.14.2.695.

Abstract

Background: Mutations affecting the epidermal growth factor receptor (EGFR) are good predictors of clinical efficacy of EGFR tyrosine kinase inhibitors (TKI) in patients with non-small cell lung cancer. Serum carcinoembryonic antigen (CEA) levels are also regarded as predictive for the efficacy of EGFR-TKI and EGFR gene mutations. This study analyzed the association between EGFR gene mutations and clinical features, including serum tumor marker levels in lung adenocarcinomas patients.

Patients and methods: A total of 70 lung adenocarcinoma patients with complete clinical data and pathological specimens were investigated. EGFR gene mutations at exons 19 and 21 were assessed. Serum tumor markers were detected by protein chip- chemiluminescence at the corresponding time, and correlations were analyzed.

Results: Mutations of the EGFR gene were detected in 27 of the 70 patients and the serum CEA and CA242 concentrations were found to be significantly associated with the incidence of EGFR gene mutations (P<0.05). The AUCs for CEA and CA242 were 0.724 (95% CI: 0.598~0.850, P<0.05) and 0.769 (95% CI: 0.523~0.800, P<0.05) respectively.

Conclusions: Serum CEA and CA242 levels are associated with mutations of the EGFR gene in patients with lung adenocarcinomas.

MeSH terms

  • Adenocarcinoma / drug therapy
  • Adenocarcinoma / genetics*
  • Adenocarcinoma of Lung
  • Aged
  • Antigens, Tumor-Associated, Carbohydrate / blood*
  • Antineoplastic Agents / therapeutic use
  • Biomarkers, Tumor / blood*
  • CA-125 Antigen / blood
  • Carcinoembryonic Antigen / blood*
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Non-Small-Cell Lung / genetics
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / genetics*
  • Erlotinib Hydrochloride
  • Female
  • Gefitinib
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / genetics*
  • Male
  • Membrane Proteins / blood
  • Mutation / genetics
  • Protein Kinase Inhibitors / therapeutic use
  • Quinazolines / therapeutic use

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • Antineoplastic Agents
  • Biomarkers, Tumor
  • CA 242 antigen
  • CA-125 Antigen
  • Carcinoembryonic Antigen
  • MUC16 protein, human
  • Membrane Proteins
  • Protein Kinase Inhibitors
  • Quinazolines
  • carbohydrate antigen 199, human
  • Erlotinib Hydrochloride
  • EGFR protein, human
  • ErbB Receptors
  • Gefitinib