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Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study - 04/01/12

Doi : 10.1016/S1470-2045(11)70302-3 
Gillian C Barnett, DrBM BCh a, c, , Charlotte E Coles, PhD b, Rebecca M Elliott, MRes d, Caroline Baynes c, Craig Luccarini, BSc c, Don Conroy c, Jennifer S Wilkinson, BSc b, Jonathan Tyrer, PhD c, Vivek Misra, MB BS e, Radka Platte, BSc c, Sarah L Gulliford, PhD f, Matthew R Sydes, MSc h, Emma Hall, PhD i, Søren M Bentzen, ProfPhD j, David P Dearnaley, ProfMD g, Neil G Burnet, PhD a, b, Paul DP Pharoah, PhD c, Alison M Dunning, PhD c, Catharine ML West, ProfPhD d
a University of Cambridge Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK 
b Oncology Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK 
c Cancer Research-UK Centre for Genetic Epidemiology and Department of Oncology, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK 
d School of Cancer and Enabling Sciences, University of Manchester, Manchester Academic Health Science Centre, Christie Hospital, Manchester, UK 
e Department of Clinical Oncology, Christie Hospital, Manchester, UK 
f Joint Department of Physics, Institute of Cancer Research and Royal Marsden NHS Foundation Trust, Sutton, UK 
g Department of Academic Urology, Institute of Cancer Research and Royal Marsden NHS Foundation Trust, Sutton, UK 
h Cancer Group, MRC Clinical Trials Unit, London, UK 
i Institute of Cancer Research Clinical Trials and Statistics Unit, Sutton, UK 
j University of Wisconsin, School of Medicine and Public Health, Department of Human Oncology, K4/316 Clinical Science Center, Madison, WI, USA 

* Correspondence to: Dr Gillian C Barnett, Cancer Research-UK Department of Oncology, Strangeways Research Laboratory, Cambridge CB1 8RN, UK

Summary

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.

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Vol 13 - N° 1

P. 65-77 - janvier 2012 Retour au numéro
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