Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study

Lancet Oncol. 2012 Jan;13(1):65-77. doi: 10.1016/S1470-2045(11)70302-3. Epub 2011 Dec 12.

Abstract

Background: Several studies have reported associations between radiation toxicity and single nucleotide polymorphisms (SNPs) in candidate genes. Few associations have been tested in independent validation studies. This prospective study aimed to validate reported associations between genotype and radiation toxicity in a large independent dataset.

Methods: 92 (of 98 attempted) SNPs in 46 genes were successfully genotyped in 1613 patients: 976 received adjuvant breast radiotherapy in the Cambridge breast IMRT trial (ISRCTN21474421, n=942) or in a prospective study of breast toxicity at the Christie Hospital, Manchester, UK (n=34). A further 637 received radical prostate radiotherapy in the MRC RT01 multicentre trial (ISRCTN47772397, n=224) or in the Conventional or Hypofractionated High Dose Intensity Modulated Radiotherapy for Prostate Cancer (CHHiP) trial (ISRCTN97182923, n=413). Late toxicity was assessed 2 years after radiotherapy with a validated photographic technique (patients with breast cancer only), clinical assessment, and patient questionnaires. Association tests of genotype with overall radiation toxicity score and individual endpoints were undertaken in univariate and multivariable analyses. At a type I error rate adjusted for multiple testing, this study had 99% power to detect a SNP, with minor allele frequency of 0·35, associated with a per allele odds ratio of 2·2.

Findings: None of the previously reported associations were confirmed by this study, after adjustment for multiple comparisons. The p value distribution of the SNPs tested against overall toxicity score was not different from that expected by chance.

Interpretation: We did not replicate previously reported late toxicity associations, suggesting that we can essentially exclude the hypothesis that published SNPs individually exert a clinically relevant effect. Continued recruitment of patients into studies within the Radiogenomics Consortium is essential so that sufficiently powered studies can be done and methodological challenges addressed.

Funding: Cancer Research UK, The Royal College of Radiologists, Addenbrooke's Charitable Trust, Breast Cancer Campaign, Cambridge National Institute of Health Research (NIHR) Biomedical Research Centre, Experimental Cancer Medicine Centre, East Midlands Innovation, the National Cancer Institute, Joseph Mitchell Trust, Royal Marsden NHS Foundation Trust, Institute of Cancer Research NIHR Biomedical Research Centre for Cancer.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / genetics*
  • Breast Neoplasms / radiotherapy*
  • Dose Fractionation, Radiation*
  • Dose-Response Relationship, Radiation
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Humans
  • Linear Models
  • Male
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Prospective Studies
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / radiotherapy*
  • Radiation Injuries / genetics*
  • Radiation Injuries / pathology
  • Radiotherapy, Adjuvant / adverse effects
  • Radiotherapy, Intensity-Modulated / adverse effects*
  • Risk Assessment
  • Risk Factors
  • Time Factors
  • United Kingdom

Associated data

  • ISRCTN/ISRCTN21474421
  • ISRCTN/ISRCTN47772397
  • ISRCTN/ISRCTN97182923