Literature DB >> 30504931

Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels.

Kristy Lee1, Bryce A Seifert1, Hermela Shimelis2, Rajarshi Ghosh3, Stephanie B Crowley1, Natalie J Carter4, Kurston Doonanco4, A Katherine Foreman1, Deborah I Ritter3, Sharisse Jimenez1, Mackenzie Trapp1, Kenneth Offit5, Sharon E Plon3, Fergus J Couch6.   

Abstract

PURPOSE: Several genes on hereditary breast and ovarian cancer susceptibility test panels have not been systematically examined for strength of association with disease. We employed the Clinical Genome Resource (ClinGen) clinical validity framework to assess the strength of evidence between selected genes and breast or ovarian cancer.
METHODS: Thirty-one genes offered on cancer panel testing were selected for evaluation. The strength of gene-disease relationship was systematically evaluated and a clinical validity classification of either Definitive, Strong, Moderate, Limited, Refuted, Disputed, or No Reported Evidence was assigned.
RESULTS: Definitive clinical validity classifications were made for 10/31 and 10/32 gene-disease pairs for breast and ovarian cancer respectively. Two genes had a Moderate classification whereas, 6/31 and 6/32 genes had Limited classifications for breast and ovarian cancer respectively. Contradictory evidence resulted in Disputed or Refuted assertions for 9/31 genes for breast and 4/32 genes for ovarian cancer. No Reported Evidence of disease association was asserted for 5/31 genes for breast and 11/32 for ovarian cancer.
CONCLUSION: Evaluation of gene-disease association using the ClinGen clinical validity framework revealed a wide range of classifications. This information should aid laboratories in tailoring appropriate gene panels and assist health-care providers in interpreting results from panel testing.

Entities:  

Keywords:  ClinGen; classification; gene test panels; gene validity; hereditary breast and ovarian cancer

Mesh:

Year:  2018        PMID: 30504931      PMCID: PMC6579711          DOI: 10.1038/s41436-018-0361-5

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  34 in total

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2.  Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.

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Journal:  Am J Hum Genet       Date:  2017-05-25       Impact factor: 11.025

3.  Increased risk of breast cancer in women with NF1.

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4.  Germline mutation in the STK11 gene in a girl with an ovarian Sertoli cell tumour.

Authors:  Guy Massa; Nele Roggen; Marleen Renard; Johan J P Gille
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5.  Germline RECQL mutations in high risk Chinese breast cancer patients.

Authors:  Ava Kwong; Vivian Y Shin; Isabella W Y Cheuk; Jiawei Chen; Chun H Au; Dona N Ho; Tsun L Chan; Edmond S K Ma; Mohammad R Akbari; Steven A Narod
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6.  Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.

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Review 7.  Gene panel testing for inherited cancer risk.

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8.  Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.

Authors:  Fergus J Couch; Hermela Shimelis; Chunling Hu; Steven N Hart; Eric C Polley; Jie Na; Emily Hallberg; Raymond Moore; Abigail Thomas; Jenna Lilyquist; Bingjian Feng; Rachel McFarland; Tina Pesaran; Robert Huether; Holly LaDuca; Elizabeth C Chao; David E Goldgar; Jill S Dolinsky
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Review 9.  Risk of breast cancer in Lynch syndrome: a systematic review.

Authors:  Aung Ko Win; Noralane M Lindor; Mark A Jenkins
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10.  Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing.

Authors:  Christine Stanislaw; Yuan Xue; William R Wilcox
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2.  Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers.

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Review 3.  Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation.

Authors:  Alvaro N Monteiro; Peter Bouwman; Arne N Kousholt; Diana M Eccles; Gael A Millot; Jean-Yves Masson; Marjanka K Schmidt; Shyam K Sharan; Ralph Scully; Lisa Wiesmüller; Fergus Couch; Maaike P G Vreeswijk
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4.  Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty.

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Review 5.  Cancer Genetic Counseling-Current Practice and Future Challenges.

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6.  Clinical validity of expanded carrier screening: Evaluating the gene-disease relationship in more than 200 conditions.

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Review 7.  Germline Missense Variants in BRCA1: New Trends and Challenges for Clinical Annotation.

Authors:  Volha A Golubeva; Thales C Nepomuceno; Alvaro N A Monteiro
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8.  Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing.

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9.  A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).

Authors:  Deborah I Ritter; Shruti Rao; Shashikant Kulkarni; Subha Madhavan; Kenneth Offit; Sharon E Plon
Journal:  Cold Spring Harb Mol Case Stud       Date:  2019-10-23

10.  Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.

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