An inflammation based score can optimize the selection of patients with advanced cancer considered for early phase clinical trials

PLoS One. 2014 Jan 7;9(1):e83279. doi: 10.1371/journal.pone.0083279. eCollection 2014.

Abstract

Background: Adequate organ function and good performance status (PS) are common eligibility criteria for phase I trials. As inflammation is pathogenic and prognostic in cancer we investigated the prognostic performance of inflammation-based indices including the neutrophil (NLR) and platelet to lymphocyte ratio (PLR).

Methods: We studied inflammatory scores in 118 unselected referrals. NLR normalization was recalculated at disease reassessment. Each variable was assessed for progression-free (PFS) and overall survival (OS) on uni- and multivariate analyses and tested for 90 days survival (90DS) prediction using receiving operator curves (ROC).

Results: We included 118 patients with median OS 4.4 months, 23% PS>1. LDH≥450 and NLR≥5 were multivariate predictors of OS (p<0.001). NLR normalization predicted for longer OS (p<0.001) and PFS (p<0.05). PS and NLR ranked as most accurate predictors of both 90DS with area under ROC values of 0.66 and 0.64, and OS with c-score of 0.69 and 0.60. The combination of NLR+PS increased prognostic accuracy to 0.72. The NLR was externally validated in a cohort of 126 subjects.

Conclusions: We identified the NLR as a validated and objective index to improve patient selection for experimental therapies, with its normalization following treatment predicting for a survival benefit of 7 months. Prospective validation of the NLR is warranted.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Blood Platelets / pathology
  • Clinical Trials as Topic / standards*
  • Female
  • Humans
  • Inflammation / diagnosis
  • Inflammation / pathology*
  • Leukocyte Count
  • Lymphocytes / pathology
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Neoplasms / mortality
  • Neoplasms / pathology*
  • Neoplasms / therapy
  • Neutrophils / pathology
  • Patient Selection*
  • Platelet Count
  • Prognosis
  • Reproducibility of Results
  • Retrospective Studies
  • Treatment Outcome
  • Tumor Burden