Peripheral lymphocyte subset variation predicts prostate cancer carbon ion radiotherapy outcomes

Oncotarget. 2016 May 3;7(18):26422-35. doi: 10.18632/oncotarget.8389.

Abstract

The immune system plays a complementary role in the cytotoxic activity of radiotherapy. Here, we examined changes in immune cell subsets after heavy ion therapy for prostate cancer. The lymphocyte counts were compared with acute radiotherapy-related toxicity, defined according to the Common Terminology Criteria for Adverse Events, and short-term local efficacy, defined based on prostate-specific antigen concentrations. Confirmed prostate cancer patients who had not received previous radiotherapy were administered carbon ion radiotherapy (CIR) in daily fractions of 2.74 GyE with a total dose of 63-66 GyE. Lymphocyte subset counts were investigated before, during and after radiotherapy, and at a 1 month follow-up. Most notable among our findings, the CD4/CD8 ratio and CD19+ cell counts were consistently higher in patients with a complete response (CR) or partial response (PR) to CIR than in those classified in the stable disease (SD) group (P<0.05 for both). But CD3+ and CD8+ cell counts were lower in the CR and PR groups than in the SD group. These results indicate that variations in peripheral lymphocyte subpopulations are predictive of outcome after CIR for prostate cancer.

Keywords: carbon ion radiotherapy; peripheral lymphocyte; prostate cancer.

Publication types

  • Clinical Trial

MeSH terms

  • Adenocarcinoma / immunology
  • Adenocarcinoma / radiotherapy*
  • Aged
  • Aged, 80 and over
  • Heavy Ion Radiotherapy / adverse effects
  • Heavy Ion Radiotherapy / methods
  • Humans
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / radiation effects
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Prostatic Neoplasms / immunology
  • Prostatic Neoplasms / radiotherapy*
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / radiation effects
  • Treatment Outcome