Systemic inflammatory markers have independent prognostic value in patients with metastatic testicular germ cell tumours undergoing first-line chemotherapy

Br J Cancer. 2018 Mar 20;118(6):825-830. doi: 10.1038/bjc.2017.467. Epub 2018 Feb 27.

Abstract

Background: The prognostic utility of systemic inflammatory markers has so far not been investigated in patients with metastatic testicular germ cell tumours (GCTs).

Methods: International Germ Cell Cancer Cooperative Group (IGCCCG) risk groups and blood-based systemic inflammatory markers (haemoglobin, leukocytes, platelets (P), neutrophils (N), lymphocytes (L), C-reactive protein (CRP) and albumin) of 146 patients undergoing first-line chemotherapy for GCT were retrieved. In addition, N to L ratio (NLR), P to L ratio and the systemic immune-inflammation index (SII=N × P/L) were calculated. The prognostic ability of these markers for overall survival (OS) were assessed using regression analyses and Kaplan-Meier curves with log-rank tests.

Results: In univariate Cox regression, low haemoglobin and albumin as well as high leukocytes, N, NLR, SII and CRP were associated with a shorter OS. In multivariable Cox regression analyses, high leukocyte (hazard ratio (HR) 1.274 (95% confidence interval (CI) 1.057-1.535); P=0.011) and N count (1.470 (1.092-1.980); P=0.011), higher NLR (84.5 (2.2-3193.4); P=0.017) and SII (12.15 (1.17-126.26); P=0.037) remained independent prognostic predictors for OS besides the IGCCCG risk groups.

Conclusions: Systemic inflammatory markers might have prognostic utility for patients with metastatic GCT. The planned IGCCCG update could be an opportunity to test these markers in a larger data set.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Blood Platelets / immunology
  • Blood Platelets / pathology
  • Cohort Studies
  • Humans
  • Immunohistochemistry
  • Inflammation / blood
  • Inflammation / immunology*
  • Inflammation / pathology
  • Kaplan-Meier Estimate
  • Lymphocytes / immunology
  • Lymphocytes / pathology
  • Male
  • Middle Aged
  • Neoplasms, Germ Cell and Embryonal / blood
  • Neoplasms, Germ Cell and Embryonal / drug therapy*
  • Neoplasms, Germ Cell and Embryonal / immunology*
  • Neoplasms, Germ Cell and Embryonal / pathology
  • Neutrophils / immunology
  • Neutrophils / pathology
  • Prognosis
  • Progression-Free Survival
  • Retrospective Studies
  • Testicular Neoplasms / blood
  • Testicular Neoplasms / drug therapy*
  • Testicular Neoplasms / immunology*
  • Testicular Neoplasms / pathology
  • Tissue Array Analysis
  • Translational Research, Biomedical
  • Young Adult

Supplementary concepts

  • Testicular Germ Cell Tumor