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The trans-DATA study: aims and design of a translational breast cancer prognostic marker identification study.

Authors :
de Ruijter TC
Smits KM
Aarts MJ
van Hellemond IEG
Van Neste L
de Vries B
Peer PGM
Veeck J
van Engeland M
Tjan-Heijnen VCG
Source :
Diagnostic and prognostic research [Diagn Progn Res] 2019 Oct 17; Vol. 3, pp. 20. Date of Electronic Publication: 2019 Oct 17 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: The effect of extended adjuvant aromatase inhibition in hormone-positive breast cancer after sequential tamoxifen, aromatase inhibitor treatment of 5 years was recently investigated by the DATA study. This study found no statistically significant effect of prolonged aromatase therapy. However, subgroup analysis showed post hoc statistically significant benefits in certain sub-populations. The trans-DATA study is a translational sub-study aiming to identify DNA methylation markers prognostic of patient outcome.<br />Methods: Patients from the DATA study are included in the trans-DATA study. Primary breast tumour tissue will be collected, subtyped and used for DNA isolation. A genome-wide DNA methylation discovery assay will be performed on 60 patients that had a distant recurrence and 60 patients that did not have a distant recurrence using the Infinium Methylation EPIC Bead Chip platform. Differentially methylated regions of interest will be selected based on Akaike's Information Criterion, Gene Ontology Analysis and correlation between methylation and expression levels. Selected candidate genes will subsequently be validated in the remaining patients using qMSP.<br />Discussion: The trans-DATA study uses a cohort derived from a clinical randomised trial. This study was designed to avoid common pitfalls in marker discovery studies such as selection bias, confounding and lack of reproducibility. In addition to the usual clinical risk factors, the results of this study may identify predictors of high recurrence risk in hormone receptor-positive breast cancer patients treated with sequential tamoxifen and aromatase inhibitor therapy.<br />Competing Interests: Competing interestsProf. dr. Tjan-Heijnen reports grants from AstraZeneca, during the conduct of the study; grants and non-financial support from Roche, grants and non-financial support from Pfizer, grants and non-financial support from Novartis, grants from Eisai, outside the submitted work. Dr. Peer reports grants from AstraZeneca, during the conduct of the study.<br /> (© The Author(s) 2019.)

Details

Language :
English
ISSN :
2397-7523
Volume :
3
Database :
MEDLINE
Journal :
Diagnostic and prognostic research
Publication Type :
Academic Journal
Accession number :
31641693
Full Text :
https://doi.org/10.1186/s41512-019-0065-6