Evaluation of an inflammation-based prognostic score in patients with advanced ovarian cancer

Eur J Cancer. 2008 Jan;44(2):251-6. doi: 10.1016/j.ejca.2007.11.011. Epub 2007 Dec 26.

Abstract

Background: There is increasing evidence that the presence of an ongoing systemic inflammatory response is associated with poor outcome in patients with advanced cancer. The aim of this study was to validate whether an inflammation-based prognostic score (Glasgow Prognostic Score, GPS) is associated with survival in patients with advanced stage (stage III/IV) ovarian cancer.

Patients and methods: An audit was conducted of patients with a new diagnosis of stage III or IV ovarian cancer presenting to the West London Gynae-Oncology Centre between October 2003 and June 2006 (n=154). The GPS was constructed as follows: Patients with both an elevated C-reactive protein (>10 mg/l) and hypoalbuminaemia (<35 g/l) were allocated a score of 2. Patients in whom only one or none of these biochemical abnormalities was present were allocated a score of 1 or 0, respectively.

Results: On univariate analysis GPS, histological type, ALP, performance status, primary surgery and ascites were predictors of overall survival. On multivariate a high GPS score, non-serous histology, high ALP and no initial surgery were independent predictors of worse overall survival in this population.

Conclusions: The presence of a systemic inflammatory response, as measured by the GPS, is an independent predictor of poor overall survival in patients with advanced ovarian cancer independent of treatment received.

Publication types

  • Evaluation Study
  • Validation Study

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • C-Reactive Protein / metabolism
  • Female
  • Humans
  • Inflammation
  • London / epidemiology
  • Middle Aged
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / mortality*
  • Ovarian Neoplasms / surgery
  • Prognosis
  • Serum Albumin / metabolism
  • Survival Analysis
  • Systemic Inflammatory Response Syndrome / mortality*

Substances

  • Serum Albumin
  • C-Reactive Protein