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Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing
The introduction of next-generation sequencing (NGS) technology in testing for hereditary cancer susceptibility allows testing of multiple cancer susceptibility genes simultaneously. While there are many potential benefits to utilizing this technology in the hereditary cancer clinic, including effic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Chinese Anti-Cancer Association
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850128/ https://www.ncbi.nlm.nih.gov/pubmed/27144062 http://dx.doi.org/10.28092/j.issn.2095-3941.2016.0002 |
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author | Stanislaw, Christine Xue, Yuan Wilcox, William R. |
author_facet | Stanislaw, Christine Xue, Yuan Wilcox, William R. |
author_sort | Stanislaw, Christine |
collection | PubMed |
description | The introduction of next-generation sequencing (NGS) technology in testing for hereditary cancer susceptibility allows testing of multiple cancer susceptibility genes simultaneously. While there are many potential benefits to utilizing this technology in the hereditary cancer clinic, including efficiency of time and cost, there are also important limitations that must be considered. The best panel for the given clinical situation should be selected to minimize the number of variants of unknown significance. The inclusion in panels of low penetrance or newly identified genes without specific actionability can be problematic for interpretation. Genetic counselors are an essential part of the hereditary cancer risk assessment team, helping the medical team select the most appropriate test and interpret the often complex results. Genetic counselors obtain an extended family history, counsel patients on the available tests and the potential implications of results for themselves and their family members (pre-test counseling), explain to patients the implications of the test results (post-test counseling), and assist in testing family members at risk. |
format | Online Article Text |
id | pubmed-4850128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Chinese Anti-Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-48501282016-05-03 Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing Stanislaw, Christine Xue, Yuan Wilcox, William R. Cancer Biol Med Review The introduction of next-generation sequencing (NGS) technology in testing for hereditary cancer susceptibility allows testing of multiple cancer susceptibility genes simultaneously. While there are many potential benefits to utilizing this technology in the hereditary cancer clinic, including efficiency of time and cost, there are also important limitations that must be considered. The best panel for the given clinical situation should be selected to minimize the number of variants of unknown significance. The inclusion in panels of low penetrance or newly identified genes without specific actionability can be problematic for interpretation. Genetic counselors are an essential part of the hereditary cancer risk assessment team, helping the medical team select the most appropriate test and interpret the often complex results. Genetic counselors obtain an extended family history, counsel patients on the available tests and the potential implications of results for themselves and their family members (pre-test counseling), explain to patients the implications of the test results (post-test counseling), and assist in testing family members at risk. Chinese Anti-Cancer Association 2016-03 /pmc/articles/PMC4850128/ /pubmed/27144062 http://dx.doi.org/10.28092/j.issn.2095-3941.2016.0002 Text en Copyright 2016 Cancer Biology & Medicine http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Review Stanislaw, Christine Xue, Yuan Wilcox, William R. Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title | Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title_full | Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title_fullStr | Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title_full_unstemmed | Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title_short | Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
title_sort | genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850128/ https://www.ncbi.nlm.nih.gov/pubmed/27144062 http://dx.doi.org/10.28092/j.issn.2095-3941.2016.0002 |
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