Tumour radiosensitivity is associated with immune activation in solid tumours

Eur J Cancer. 2017 Oct:84:304-314. doi: 10.1016/j.ejca.2017.08.001. Epub 2017 Aug 29.

Abstract

Purpose: Our goal was to determine whether tumour radiosensitivity is associated with activation of the immune system across all tumour types as measured by two gene expression signatures (GESs).

Methods: We identified 10,240 genomically profiled distinct solid primary tumours with gene expression analysis available from an institutional de-identified database. Two separate GESs were included in the analysis, the radiosensitivity index (RSI) GES (a 10-gene GES as a measure of radiosensitivity) and the 12-chemokine (12-CK) signature (a 12-gene GES as a measure of immune activation). We tested whether the RSI and 12-CK were associated with each other across all tumour samples and, in an exploratory analysis, their prognostic significance in predicting distant metastasis-free survival (DMFS) among a well-characterised, independent cohort of 282 early-stage breast cancer cases treated with surgery and post-operative radiation alone without systemic therapy. The lower the RSI score, the higher the tumour radiosensitivity; whereas, the higher the 12-CK score the higher the immune activation.

Results: Using an RSI cut-point of ≤0.3745, RSI-low tumours (n = 4,291, 41.9%) had a significantly higher median 12-CK GES value (0.54 [-0.136, 1.095]) compared with RSI-high tumours (-0.17 [-0.82, 0.42]; p < 0.001) across all tumour samples, indicating that radiosensitivity is associated with immune activation. In an exploratory analysis of early-stage breast cancer cases, a multivariable model with patient age, RSI and 12-CK provided a strong composite model for DMFS (p = 0.02), with RSI (hazard ratio [HR] 0.63 [95% confidence interval 0.36, 1.09]) and 12-CK (HR 0.66 [0.41, 1.04]) each providing comparable contributions.

Conclusions: Tumour radiosensitivity is associated with immune activation as measured by the two GESs.

Keywords: Cancer; Immune; Radiation; Radiosensitivity; Survival.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / immunology*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / immunology
  • Breast Neoplasms / mortality
  • Breast Neoplasms / radiotherapy*
  • Chemokines / genetics
  • Chemokines / immunology*
  • Databases, Genetic
  • Disease-Free Survival
  • Gene Expression Profiling
  • Genetic Predisposition to Disease
  • Humans
  • Kaplan-Meier Estimate
  • Netherlands
  • Phenotype
  • Proportional Hazards Models
  • Radiation Tolerance / genetics
  • Radiation Tolerance / immunology*
  • Radiotherapy, Adjuvant
  • Risk Factors
  • Time Factors
  • Transcriptome
  • Treatment Outcome
  • Tumor Microenvironment

Substances

  • Biomarkers, Tumor
  • Chemokines