Clinical impact of pleural fluid carcinoembryonic antigen on therapeutic strategy and efficacy in lung adenocarcinoma patients with malignant pleural effusion

Korean J Intern Med. 2024 Mar;39(2):318-326. doi: 10.3904/kjim.2023.309. Epub 2024 Feb 14.

Abstract

Background/aims: Epidermal growth factor receptor (EGFR) mutation is important in determining the treatment strategy for advanced lung cancer patients with malignant pleural effusion (MPE). Contrary to serum carcinoembryonic antigen (S-CEA) levels, the associations between pleural fluid CEA (PF-CEA) levels and EGFR mutation status as well as between PF-CEA levels and treatment efficacy have rarely been investigated in lung adenocarcinoma patients with MPE.

Methods: This retrospective study enrolled lung adenocarcinoma patients with MPE and available PF-CEA levels and EGFR mutation results. The patients were categorized based on PF-CEA levels: < 10 ng/mL, 10-100 ng/mL, 100-500 ng/mL, and ≥ 500 ng/mL. The association between PF-CEA levels and EGFR mutation status as well as their therapeutic impact on overall survival was compared among the four groups.

Results: This study included 188 patients. PF-CEA level was found to be an independent predictor of EGFR mutation but not S-CEA level. The EGFR mutation rates were higher as the PF-CEA levels increased, regardless of cytology results or sample types. Among EGFR-mutant lung adenocarcinoma patients receiving EGFR-tyrosine kinase inhibitor (TKI) treatment, those with high PF-CEA levels had significantly better survival outcomes than those with low PF-CEA levels.

Conclusion: High PF-CEA levels were associated with high EGFR mutation rate and may lead to a favorable clinical outcome of EGFR-TKI treatment in EGFR-mutant lung adenocarcinoma patients with MPE. These findings highlight the importance of actively investigating EGFR mutation detection in patients with suspected MPE and elevated PF-CEA levels despite negative cytology results.

Keywords: Epidermal growth factor receptor; Malignant pleural effusion; Mutation; Pleural fluid–carcinoembryonic antigen; Tyrosine kinase inhibitor.

MeSH terms

  • Adenocarcinoma of Lung* / drug therapy
  • Adenocarcinoma of Lung* / genetics
  • Adenocarcinoma of Lung* / pathology
  • Carcinoembryonic Antigen / genetics
  • Carcinoembryonic Antigen / therapeutic use
  • ErbB Receptors / genetics
  • Humans
  • Lung Neoplasms* / drug therapy
  • Mutation
  • Pleural Effusion* / chemically induced
  • Pleural Effusion* / diagnosis
  • Pleural Effusion* / drug therapy
  • Pleural Effusion, Malignant* / diagnosis
  • Pleural Effusion, Malignant* / etiology
  • Pleural Effusion, Malignant* / therapy
  • Protein Kinase Inhibitors / therapeutic use
  • Retrospective Studies

Substances

  • Carcinoembryonic Antigen
  • Protein Kinase Inhibitors
  • ErbB Receptors