Literature DB >> 21962891

Which individuals undergoing BRACAnalysis need BART testing?

Kristen M Shannon1, Linda H Rodgers, Gayun Chan-Smutko, Devanshi Patel, Michele Gabree, Paula D Ryan.   

Abstract

Deleterious mutations in BRCA1 and BRCA2 include those identified by sequencing technology as well as large genomic rearrangements (LGR). The main testing laboratory in the United States, Myriad Genetics Laboratory (MGL), has defined criteria for inclusion of LGR testing (i.e., BRACAnalysis Rearrangement Test, or BART™) when BRCA1 and BRCA2 testing is ordered. We were interested in determining how many of our patients with LGR mutations in BRCA1 and BRCA2 fulfilled these MGL criteria. A retrospective chart review was performed on all individuals who underwent genetic testing at our institution since August 2006. Individuals who underwent LGR testing were classified as either having or not having a LGR in BRCA1 or BRCA2. Each individual's history was classified as meeting MGL defined LGR criteria, meeting criteria using third-degree relatives, or not meeting criteria. A total of 257 BART tests were ordered at our institution from August 2006 to August 2009. Five individuals (1.9%) had an LGR mutation. Two LGR were identified in patients who met MGL defined LGR criteria. One LGR was identified in a patient that met MGL defined LGR criteria only when using third-degree relatives. Two LGR were identified in individuals who did not meet MGL defined criteria. LGR are present in individuals who do not have a high pretest probability of carrying a mutation in BRCA1 or BRCA2. These data suggest that when BRCA1 and BRCA2 genetic testing is performed, testing should always include LGR testing so that the results are the most comprehensive and reliable.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21962891     DOI: 10.1016/j.cancergen.2011.07.005

Source DB:  PubMed          Journal:  Cancer Genet


  3 in total

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Journal:  J Community Genet       Date:  2013-08-29

Review 2.  Genetic tests to identify risk for breast cancer.

Authors:  Julie A Lynch; Vickie Venne; Brygida Berse
Journal:  Semin Oncol Nurs       Date:  2015-02-26       Impact factor: 2.315

3.  A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer.

Authors:  Tuya Pal; Deborah Cragun; Courtney Lewis; Andrea Doty; Maria Rodriguez; Cristi Radford; Zachary Thompson; Jongphil Kim; Susan T Vadaparampil
Journal:  Genet Test Mol Biomarkers       Date:  2013-02-28
  3 in total

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