Title |
Cancer Risk Assessment Using Genetic Panel Testing: Considerations for Clinical Application
|
---|---|
Published in |
Journal of Genetic Counseling, March 2014
|
DOI | 10.1007/s10897-014-9695-6 |
Pubmed ID | |
Authors |
Susan Hiraki, Erica S. Rinella, Freya Schnabel, Ruth Oratz, Harry Ostrer |
Abstract |
With the completion of the Human Genome Project and the development of high throughput technologies, such as next-generation sequencing, the use of multiplex genetic testing, in which multiple genes are sequenced simultaneously to test for one or more conditions, is growing rapidly. Reflecting underlying heterogeneity where a broad range of genes confer risks for one or more cancers, the development of genetic cancer panels to assess these risks represents just one example of how multiplex testing is being applied clinically. There are a number of issues and challenges to consider when conducting genetic testing for cancer risk assessment, and these issues become exceedingly more complex when moving from the traditional single-gene approach to panel testing. Here, we address the practical considerations for clinical use of panel testing for breast, ovarian, and colon cancers, including the benefits, limitations and challenges, genetic counseling issues, and management guidelines. |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 3 | 5% |
Unknown | 56 | 95% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Master | 14 | 24% |
Researcher | 10 | 17% |
Student > Ph. D. Student | 7 | 12% |
Professor > Associate Professor | 6 | 10% |
Other | 5 | 8% |
Other | 12 | 20% |
Unknown | 5 | 8% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 20 | 34% |
Biochemistry, Genetics and Molecular Biology | 13 | 22% |
Agricultural and Biological Sciences | 10 | 17% |
Social Sciences | 3 | 5% |
Psychology | 2 | 3% |
Other | 3 | 5% |
Unknown | 8 | 14% |