Can flow cytometry reinvent the sentinel lymph node concept in gastric cancer patients?

J Surg Res. 2018 Mar:223:46-57. doi: 10.1016/j.jss.2017.10.018. Epub 2017 Nov 10.

Abstract

Background: The focused sentinel lymph node (SLN) concept we proposed previously relied on real time-quantitative polymerase chain reaction (RT-qPCR) to detect tumor cells, which is too elaborate for intraoperative use. Therefore, we evaluated flow cytometry for intraoperative detection of tumor cells in SLNs.

Methods: Sixty-five consecutive gastric cancer patients were included. SLN analysis was carried out for a single SLN from each patient, using the molecular methods of RT-qPCR (first 30 patients) and flow cytometry (final 35 patients). All LNs underwent hematoxylin and eosin staining and immunohistochemical examination.

Results: Extraction of the SLN from a high-risk station was an important determinant for accurate prediction of LN metastases. For RT-qPCR, the sensitivity and specificity of detection were 72.7% and 81.8%, respectively, and for flow cytometry, 36.8% and 100%, respectively. When only high-risk SLNs were analyzed and specimens with <10% viability of leukocytes were excluded, the sensitivity and specificity of flow cytometry were 60% and 100%, respectively. Multivariate analysis identified significant predictors for LN metastases as the molecular method of SLN analysis (P = 0.021; 95% confidence interval [CI]: 1.304-24.284) and lymphovascular invasion (P = 0.002; 95% CI: 2.142-28.555). In subgroup analysis of high-risk SLNs, only RT-qPCR was a significant predictor for LN metastases (P = 0.016; 95% CI: 1.581-91.084).

Conclusions: Flow cytometry of high-risk SLNs, excluding specimens with low cell viability is a rapid, cost-effective, widely obtainable, and highly specific method for SLN metastases detection although it lacks the necessary sensitivity. Therefore, it cannot be recommended as a stand-alone method for the detection of LN metastases during operations.

Keywords: CEA; CK20; EpCAM; Flow cytometry; Gastric cancer; RT-qPCR; Sentinel lymph node.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Carcinoembryonic Antigen / analysis
  • Carcinoembryonic Antigen / genetics
  • Epithelial Cell Adhesion Molecule / analysis
  • Female
  • Flow Cytometry / methods*
  • Humans
  • Keratin-20 / genetics
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Sentinel Lymph Node / pathology*
  • Stomach Neoplasms / pathology*

Substances

  • Carcinoembryonic Antigen
  • EPCAM protein, human
  • Epithelial Cell Adhesion Molecule
  • KRT20 protein, human
  • Keratin-20