Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers.


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
01 07 2021
Historique:
received: 14 05 2020
revised: 17 09 2020
accepted: 08 12 2020
pubmed: 30 12 2020
medline: 25 2 2022
entrez: 29 12 2020
Statut: ppublish

Résumé

Genome-wide association studies suggest that the combined effects of breast cancer (BC)-associated single nucleotide polymorphisms (SNPs) can improve BC risk stratification using polygenic risk scores (PRSs). The performance of PRSs in genome-wide association studies-independent clinical cohorts is poorly studied in individuals carrying mutations in moderately penetrant BC predisposition genes such as CHEK2. A total of 760 female CHEK2 mutation carriers were included; 561 women were affected with BC, of whom 74 developed metachronous contralateral BC (mCBC). For PRS calculations, 2 SNP sets covering 77 (SNP set 1, developed for BC risk stratification in women unselected for their BRCA1/2 germline mutation status) and 88 (SNP set 2, developed for BC risk stratification in female BRCA1/2 mutation carriers) BC-associated SNPs were used. All statistical tests were 2-sided. Both SNP sets provided concordant PRS results at the individual level (r = 0.91, P < 2.20 × 10-16). Weighted cohort Cox regression analyses revealed statistically significant associations of PRSs with the risk for first BC. For SNP set 1, a hazard ratio of 1.71 per SD of the PRS was observed (95% confidence interval = 1.36 to 2.15, P = 3.87 × 10-6). PRSs identify a subgroup of CHEK2 mutation carriers with a predicted lifetime risk for first BC that exceeds the surveillance thresholds defined by international guidelines. Association of PRS with mCBC was examined via Cox regression analysis (SNP set 1 hazard ratio = 1.23, 95% confidence interval = 0.86 to 1.78, P = .26). PRSs may be used to personalize risk-adapted preventive measures for women with CHEK2 mutations. Larger studies are required to assess the role of PRSs in mCBC predisposition.

Sections du résumé

BACKGROUND
Genome-wide association studies suggest that the combined effects of breast cancer (BC)-associated single nucleotide polymorphisms (SNPs) can improve BC risk stratification using polygenic risk scores (PRSs). The performance of PRSs in genome-wide association studies-independent clinical cohorts is poorly studied in individuals carrying mutations in moderately penetrant BC predisposition genes such as CHEK2.
METHODS
A total of 760 female CHEK2 mutation carriers were included; 561 women were affected with BC, of whom 74 developed metachronous contralateral BC (mCBC). For PRS calculations, 2 SNP sets covering 77 (SNP set 1, developed for BC risk stratification in women unselected for their BRCA1/2 germline mutation status) and 88 (SNP set 2, developed for BC risk stratification in female BRCA1/2 mutation carriers) BC-associated SNPs were used. All statistical tests were 2-sided.
RESULTS
Both SNP sets provided concordant PRS results at the individual level (r = 0.91, P < 2.20 × 10-16). Weighted cohort Cox regression analyses revealed statistically significant associations of PRSs with the risk for first BC. For SNP set 1, a hazard ratio of 1.71 per SD of the PRS was observed (95% confidence interval = 1.36 to 2.15, P = 3.87 × 10-6). PRSs identify a subgroup of CHEK2 mutation carriers with a predicted lifetime risk for first BC that exceeds the surveillance thresholds defined by international guidelines. Association of PRS with mCBC was examined via Cox regression analysis (SNP set 1 hazard ratio = 1.23, 95% confidence interval = 0.86 to 1.78, P = .26).
CONCLUSIONS
PRSs may be used to personalize risk-adapted preventive measures for women with CHEK2 mutations. Larger studies are required to assess the role of PRSs in mCBC predisposition.

Identifiants

pubmed: 33372680
pii: 6054801
doi: 10.1093/jnci/djaa203
pmc: PMC8246885
doi:

Substances chimiques

Checkpoint Kinase 2 EC 2.7.1.11
CHEK2 protein, human EC 2.7.11.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

893-899

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Références

Genet Epidemiol. 2005 Jul;29(1):1-11
pubmed: 15880399
Nat Genet. 2013 Apr;45(4):353-61, 361e1-2
pubmed: 23535729
Nat Genet. 2013 Apr;45(4):345-8
pubmed: 23535722
Nat Genet. 2015 Apr;47(4):373-80
pubmed: 25751625
Gigascience. 2015 Feb 25;4:7
pubmed: 25722852
Cancer Epidemiol Biomarkers Prev. 2018 Apr;27(4):380-394
pubmed: 29382703
Lancet. 2013 May 25;381(9880):1827-34
pubmed: 23639488
Nat Genet. 2015 Feb;47(2):164-71
pubmed: 25581431
Nature. 2007 Jun 28;447(7148):1087-93
pubmed: 17529967
Nat Commun. 2020 Dec 14;11(1):6383
pubmed: 33318493
J Natl Cancer Inst. 2017 Oct 1;109(10):
pubmed: 28521362
Bioinformatics. 2007 May 15;23(10):1294-6
pubmed: 17384015
Int J Cancer. 2019 Oct 1;145(7):1782-1797
pubmed: 31050813
J Clin Oncol. 2016 Aug 10;34(23):2750-60
pubmed: 27269948
Genet Med. 2019 Aug;21(8):1708-1718
pubmed: 30643217
Cancer Epidemiol Biomarkers Prev. 2017 Jan;26(1):126-135
pubmed: 27697780
N Engl J Med. 2012 Nov 22;367(21):1998-2005
pubmed: 23171096
J Natl Cancer Inst. 2015 Apr 08;107(5):
pubmed: 25855707
J Clin Oncol. 2012 Dec 10;30(35):4308-16
pubmed: 23109706
Ann Transl Med. 2018 Apr;6(7):121
pubmed: 29955581
Am J Hum Genet. 2019 Jan 3;104(1):21-34
pubmed: 30554720
Nat Genet. 2013 Apr;45(4):349-51
pubmed: 23535723
Genet Med. 2017 May;19(5):599-603
pubmed: 27711073
J Intern Med. 2012 Apr;271(4):321-30
pubmed: 22292490
Br J Cancer. 2011 May 10;104(10):1656-63
pubmed: 21468051
J Med Genet. 2016 Jul;53(7):465-71
pubmed: 26928436
J Natl Cancer Inst. 2017 Jul 1;109(7):
pubmed: 28376175

Auteurs

Julika Borde (J)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Corinna Ernst (C)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Barbara Wappenschmidt (B)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Dieter Niederacher (D)

Department of Gynecology and Obstetrics, University Hospital Duesseldorf, Heinrich-Heine University Duesseldorf, Duesseldorf, Germany.

Konstantin Weber-Lassalle (K)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Gunnar Schmidt (G)

Institute of Human Genetics, Hannover Medical School, Hannover, Germany.

Jan Hauke (J)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Anne S Quante (AS)

Department of Gynecology and Obstetrics, Technical University Munich, University Hospital Rechts der Isar, Munich, Germany.

Nana Weber-Lassalle (N)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Judit Horváth (J)

Institute for Human Genetics, University Hospital Muenster, Muenster, Germany.

Esther Pohl-Rescigno (E)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Norbert Arnold (N)

Institute of Clinical Molecular Biology, Department of Gynaecology and Obstetrics, University Hospital of Schleswig-Holstein, Campus Kiel, Christian-Albrechts University Kiel, Kiel, Germany.

Andreas Rump (A)

Institute for Clinical Genetics, Technische Universitaet Dresden, Dresden, Germany.

Andrea Gehrig (A)

Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.

Julia Hentschel (J)

Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.

Ulrike Faust (U)

Institute of Medical Genetics and Applied Genomics, University Hospital Tuebingen, Tuebingen, Germany.

Véronique Dutrannoy (V)

Institute of Medical and Human Genetics, Charité Universitätsmedizin Berlin, Berlin, Germany.

Alfons Meindl (A)

Department of Gynecology and Obstetrics, Ludwig-Maximilians-University Munich, University Hospital Munich, Munich, Germany.

Maria Kuzyakova (M)

Institute of Human Genetics, University Medical Center, Georg August University, Goettingen, Germany.

Shan Wang-Gohrke (S)

Department of Gynaecology and Obstetrics, University Hospital Ulm, Ulm, Germany.

Bernhard H F Weber (BHF)

Institute of Human Genetics, University of Regensburg, Regensburg, Germany.
Institute of Clinical Human Genetics, University Hospital Regensburg, Regensburg, Germany.

Christian Sutter (C)

Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.

Alexander E Volk (AE)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Olga Giannakopoulou (O)

Division of Psychiatry, University College London, London, UK.
UCL Genetics Institute, University College London, London, UK.

Andrew Lee (A)

Department of Public Health and Primary Care, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, UK.

Christoph Engel (C)

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.

Marjanka K Schmidt (MK)

Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Antonis C Antoniou (AC)

Department of Public Health and Primary Care, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, UK.

Rita K Schmutzler (RK)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Karoline Kuchenbaecker (K)

Division of Psychiatry, University College London, London, UK.
UCL Genetics Institute, University College London, London, UK.

Eric Hahnen (E)

Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH