학술논문
The BRCA1c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
Document Type
Article
Author
Moghadasi, Setareh; Meeks, Huong D; Vreeswijk, Maaike PG; Janssen, Linda AM; Borg, Åke; Ehrencrona, Hans; Paulsson-Karlsson, Ylva; Wappenschmidt, Barbara; Engel, Christoph; Gehrig, Andrea; Arnold, Norbert; Hansen, Thomas Van Overeem; Thomassen, Mads; Jensen, Uffe Birk; Kruse, Torben A; Ejlertsen, Bent; Gerdes, Anne-Marie; Pedersen, Inge Søkilde; Caputo, Sandrine M; Couch, Fergus; Hallberg, Emily J; van den Ouweland, Ans MW; CollÅée, Margriet J; Teugels, Erik; Adank, Muriel A; van der Luijt, Rob B; Mensenkamp, Arjen R; Oosterwijk, Jan C; Blok, Marinus J; Janin, Nicolas; Claes, Kathleen BM; Tucker, Kathy; Viassolo, Valeria; Toland, Amanda Ewart; Eccles, Diana E; Devilee, Peter; Van Asperen, Christie J; Spurdle, Amanda B; Goldgar, David E; GarcÅéóía, Encarna GÅéómez
Source
Journal of Medical Genetics (JMG); 2018, Vol. 55 Issue: 1 p15-20, 6p
Subject
Language
ISSN
00222593; 14686244
Abstract
BackgroundWe previously showed that the BRCA1variant c.5096G>A p.Arg1699Gln (R1699Q) was associated with an intermediate risk of breast cancer (BC) and ovarian cancer (OC). This study aimed to assess these cancer risks for R1699Q carriers in a larger cohort, including follow-up of previously studied families, to further define cancer risks and to propose adjusted clinical management of female BRCA1*R1699Q carriers.MethodsData were collected from 129 BRCA1*R1699Q families ascertained internationally by ENIGMA (Evidence-based Network for the Interpretation of Germline Mutant Alleles) consortium members. A modified segregation analysis was used to calculate BC and OC risks. Relative risks were calculated under both monogenic model and major gene plus polygenic model assumptions.ResultsIn this cohort the cumulative risk of BC and OC by age 70 years was 20% and 6%, respectively. The relative risk for developing cancer was higher when using a model that included the effects of both the R1699Q variant and a residual polygenic component compared with monogenic model (for BC 3.67 vs 2.83, and for OC 6.41 vs 5.83).ConclusionOur results confirm that BRCA1*R1699Q confers an intermediate risk for BC and OC. Breast surveillance for female carriers based on mammogram annually from age 40 is advised. Bilateral salpingo-oophorectomy should be considered based on family history.