Soluble interleukin-2 receptors in patients with nasopharyngeal carcinoma

Cancer. 1991 Apr 15;67(8):2180-5. doi: 10.1002/1097-0142(19910415)67:8<2180::aid-cncr2820670829>3.0.co;2-t.

Abstract

The authors performed a retrospective analysis of serum soluble interleukin-2 receptor (sIL-2R) levels in 72 patients with nasopharyngeal carcinoma (NPC) using an enzyme immunoassay. Their objectives were to determine the value of serum sIL-2R in estimating the tumor burden, and its predictive value in response to therapy and prognosis. The data showed that serum sIL-2R levels in patients were significantly higher than that of healthy controls. The serum levels correlated with clinical staging and hence the tumor burden of NPC. Serial measurement of serum sIL-2R provided an accurate prognostic index of the clinical response to radiotherapy in at least 89% of patients with raised serum sIL-2R at initial diagnosis (defined as mean + 2 SD of healthy controls) and a reliable predictive index in all patients who subsequently developed distant metastasis despite initial radiotherapy. Simultaneous measurement of Epstein-Barr virus-related serology (IgA-VCA and IgG-EA) failed to demonstrate predictive value comparable with that of serum sIL-2R. The authors conclude that monitoring serum sIL-2R levels has clinical and prognostic significance in patients with NPC and that prospective studies are indicated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Carcinoma / blood
  • Carcinoma / pathology
  • Carcinoma / radiotherapy
  • Carcinoma / secondary
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Herpesvirus 4, Human / immunology
  • Humans
  • Immunoglobulin A / analysis
  • Immunoglobulin G / analysis
  • Male
  • Middle Aged
  • Monitoring, Physiologic
  • Nasopharyngeal Neoplasms / blood*
  • Nasopharyngeal Neoplasms / pathology
  • Nasopharyngeal Neoplasms / radiotherapy
  • Neoplasm Staging
  • Predictive Value of Tests
  • Receptors, Interleukin-2 / blood*
  • Retrospective Studies

Substances

  • Immunoglobulin A
  • Immunoglobulin G
  • Receptors, Interleukin-2