Literature DB >> 23615697

BRCA1/2 sequence variants of uncertain significance: a primer for providers to assist in discussions and in medical management.

Noralane M Lindor1, David E Goldgar, Sean V Tavtigian, Sharon E Plon, Fergus J Couch.   

Abstract

INTRODUCTION: DNA variants of uncertain significance (VUS) are common outcomes of clinical genetic testing for susceptibility to cancer. A statistically rigorous model that provides a pathogenicity score for each variant has been developed to aid in the clinical management of patients undergoing genetic testing.
METHODS: The information in this article is derived from multiple publications on VUS in BRCA genes, distilled for communicating with clinicians who may encounter VUS in their practice.
RESULTS: The posterior probability scores for BRCA1 or BRCA2 VUS, calculated from a multifactorial likelihood model, are explained, and links for looking up specific VUS are provided. The International Agency on Cancer Research (IARC) of the World Health Organization has proposed a simple five-tier system for clinical management that is not widely known to clinicians. Classes 1 and 2 in this system are managed as neutral variants, classes 4 and 5 are managed as pathogenic variants, and class 3 variants still have insufficient evidence to move to either end of this scale and, thus, cannot be used in medical management.
CONCLUSIONS: Development of models that integrate multiple independent lines of evidence has allowed classification of a growing number of VUS in the BRCA1 and BRCA2 genes. The pathogenicity score that is generated by this model maps to the IARC system for clinical management, which will assist clinicians in the medical management of those patients who obtain a VUS result upon testing.

Entities:  

Keywords:  BRCA1; BRCA2; Counseling; Likelihood; Management; Multifactorial

Mesh:

Substances:

Year:  2013        PMID: 23615697      PMCID: PMC3662842          DOI: 10.1634/theoncologist.2012-0452

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  50 in total

1.  Predicting deleterious amino acid substitutions.

Authors:  P C Ng; S Henikoff
Journal:  Genome Res       Date:  2001-05       Impact factor: 9.043

2.  A full-likelihood method for the evaluation of causality of sequence variants from family data.

Authors:  Deborah Thompson; Douglas F Easton; David E Goldgar
Journal:  Am J Hum Genet       Date:  2003-07-29       Impact factor: 11.025

3.  Characterization of common BRCA1 and BRCA2 variants.

Authors:  Amie M Deffenbaugh; Thomas S Frank; Michael Hoffman; Lisa Cannon-Albright; Susan L Neuhausen
Journal:  Genet Test       Date:  2002

4.  Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.

Authors:  V Abkevich; A Zharkikh; A M Deffenbaugh; D Frank; Y Chen; D Shattuck; M H Skolnick; A Gutin; S V Tavtigian
Journal:  J Med Genet       Date:  2004-07       Impact factor: 6.318

5.  Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2.

Authors:  David E Goldgar; Douglas F Easton; Amie M Deffenbaugh; Alvaro N A Monteiro; Sean V Tavtigian; Fergus J Couch
Journal:  Am J Hum Genet       Date:  2004-08-02       Impact factor: 11.025

6.  Functional evaluation and cancer risk assessment of BRCA2 unclassified variants.

Authors:  Kangjian Wu; Shannon R Hinson; Akihiro Ohashi; Daniel Farrugia; Patricia Wendt; Sean V Tavtigian; Amie Deffenbaugh; David Goldgar; Fergus J Couch
Journal:  Cancer Res       Date:  2005-01-15       Impact factor: 12.701

7.  Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families.

Authors:  A A Tesoriero; E M Wong; M A Jenkins; J L Hopper; M A Brown; G Chenevix-Trench; A B Spurdle; M C Southey
Journal:  Hum Mutat       Date:  2005-11       Impact factor: 4.878

8.  Classification of BRCA1 missense variants of unknown clinical significance.

Authors:  C M Phelan; V Dapic; B Tice; R Favis; E Kwan; F Barany; S Manoukian; P Radice; R B van der Luijt; B P M van Nesselrooij; G Chenevix-Trench; T Caldes; M de la Hoya; S Lindquist; S V Tavtigian; D Goldgar; A Borg; S A Narod; A N A Monteiro
Journal:  J Med Genet       Date:  2005-02       Impact factor: 6.318

9.  Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry.

Authors:  Rita Nanda; L Philip Schumm; Shelly Cummings; James D Fackenthal; Lise Sveen; Foluso Ademuyiwa; Melody Cobleigh; Laura Esserman; Noralane M Lindor; Susan L Neuhausen; Olufunmilayo I Olopade
Journal:  JAMA       Date:  2005-10-19       Impact factor: 56.272

10.  A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.

Authors:  Lucia Guidugli; Vernon S Pankratz; Namit Singh; James Thompson; Catherine A Erding; Christoph Engel; Rita Schmutzler; Susan Domchek; Katherine Nathanson; Paolo Radice; Christian Singer; Patricia N Tonin; Noralane M Lindor; David E Goldgar; Fergus J Couch
Journal:  Cancer Res       Date:  2012-10-29       Impact factor: 12.701

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  43 in total

1.  Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing.

Authors:  C L Scherr; N M Lindor; T L Malo; F J Couch; S T Vadaparampil
Journal:  Clin Genet       Date:  2015-02-26       Impact factor: 4.438

Review 2.  BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.

Authors:  D M Eccles; G Mitchell; A N A Monteiro; R Schmutzler; F J Couch; A B Spurdle; E B Gómez-García
Journal:  Ann Oncol       Date:  2015-07-07       Impact factor: 32.976

3.  Current condition of genetic medicine for hereditary breast cancer.

Authors:  Hiroko Terui-Kohbata; Masayuki Yoshida
Journal:  Mol Clin Oncol       Date:  2017-05-12

Review 4.  Epidemiology of Patients with Ovarian Cancer with and Without a BRCA1/2 Mutation.

Authors:  Elisabete Weiderpass; Jerzy E Tyczynski
Journal:  Mol Diagn Ther       Date:  2015-12       Impact factor: 4.074

5.  Clinical tumor sequencing: an incidental casualty of the American College of Medical Genetics and Genomics recommendations for reporting of incidental findings.

Authors:  D Williams Parsons; Angshumoy Roy; Sharon E Plon; Sameek Roychowdhury; Arul M Chinnaiyan
Journal:  J Clin Oncol       Date:  2014-06-23       Impact factor: 44.544

6.  Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variant.

Authors:  Taraka R Donti; Ruchi Masand; Daryl A Scott; William J Craigen; Brett H Graham
Journal:  Mol Genet Metab       Date:  2016-07-25       Impact factor: 4.797

7.  Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System.

Authors:  Hélène Tubeuf; Sandrine M Caputo; Teresa Sullivan; Julie Rondeaux; Sophie Krieger; Virginie Caux-Moncoutier; Julie Hauchard; Gaia Castelain; Alice Fiévet; Laëtitia Meulemans; Françoise Révillion; Mélanie Léoné; Nadia Boutry-Kryza; Capucine Delnatte; Marine Guillaud-Bataille; Linda Cleveland; Susan Reid; Eileen Southon; Omar Soukarieh; Aurélie Drouet; Daniela Di Giacomo; Myriam Vezain; Françoise Bonnet-Dorion; Violaine Bourdon; Hélène Larbre; Danièle Muller; Pascal Pujol; Fátima Vaz; Séverine Audebert-Bellanger; Chrystelle Colas; Laurence Venat-Bouvet; Angela R Solano; Dominique Stoppa-Lyonnet; Claude Houdayer; Thierry Frebourg; Pascaline Gaildrat; Shyam K Sharan; Alexandra Martins
Journal:  Cancer Res       Date:  2020-07-08       Impact factor: 12.701

Review 8.  Family-Specific Variants and the Limits of Human Genetics.

Authors:  Brian H Shirts; Colin C Pritchard; Tom Walsh
Journal:  Trends Mol Med       Date:  2016-10-11       Impact factor: 11.951

9.  Spliceogenic analysis of BRCA1 c.439T>C (rs794727800) variant by High Resolution Melting Analysis.

Authors:  Angelo Minucci; Giorgia Mazzuccato; Marco D'Indinosante; Lucia Di Nardo; Paola Concolino; Maria De Bonis; Andrea Urbani; Giovanni Scambia; Anna Fagotti; Ettore Capoluongo
Journal:  Mol Biol Rep       Date:  2019-12-12       Impact factor: 2.316

Review 10.  Understanding patient and provider perceptions and expectations of genomic medicine.

Authors:  Michael J Hall; Andrea D Forman; Susan V Montgomery; Kim L Rainey; Mary B Daly
Journal:  J Surg Oncol       Date:  2014-07-03       Impact factor: 3.454

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