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GWAS Study

Meta-analysis of three genome-wide association studies identifies two loci that predict survival and treatment outcome in breast cancer.

Khan S, Fagerholm R, Kadalayil L et al.

29423119 PubMed ID
GWAS Study Type
3136 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KS
Khan S
FR
Fagerholm R
KL
Kadalayil L
TW
Tapper W
AK
Aittomäki K
LJ
Liu J
BC
Blomqvist C
ED
Eccles D
NH
Nevanlinna H
Chapter II

Abstract

Summary of the research findings

The majority of breast cancers are driven by the female hormone oestrogen via oestrogen receptor (ER) alpha. ER-positive patients are commonly treated with adjuvant endocrine therapy, however, resistance is a common occurrence and aside from ER-status, no unequivocal predictive biomarkers are currently in clinical use. In this study, we aimed to identify constitutional genetic variants influencing breast cancer survival among ER-positive patients and specifically, among endocrine-treated patients. We conducted a meta-analysis of three genome-wide association studies comprising in total 3,136 patients with ER-positive breast cancer of which 2,751 had received adjuvant endocrine therapy. We identified a novel locus (rs992531 at 8p21.2) associated with reduced survival among the patients with ER-positive breast cancer (P = 3.77 × 10-8). Another locus (rs7701292 at 5q21.3) was associated with reduced survival among the endocrine-treated patients (P = 2.13 × 10-8). Interaction analysis indicated that the survival association of rs7701292 is treatment-specific and independent of conventional prognostic markers. In silico functional studies suggest plausible biological mechanisms for the observed survival associations and a functional link between the putative target genes of the rs992531 and rs7701292 (RHOBTB2 and RAB9P1, respectively). We further explored the genetic interaction between rs992531 and rs7701292 and found a significant, treatment-specific interactive effect on survival among ER-positive, endocrine-treated patients (hazard ratio = 6.97; 95% confidence interval, 1.79-27.08, Pinteraction= 0.036). This is the first study to identify a genetic interaction that specifically predicts treatment outcome. These findings may provide predictive biomarkers based on germ line genotype informing more personalized treatment selection.

2,971 European ancestry individuals, 165 individuals

Chapter III

Study Statistics

Key metrics and study information

3136
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Germany, Finland, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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