期刊
CURRENT TREATMENT OPTIONS IN ONCOLOGY
卷 18, 期 5, 页码 -出版社
SPRINGER
DOI: 10.1007/s11864-017-0468-y
关键词
BRCA1/2; ATM; CHEK2; PALB2; Multiple-gene testing; Hereditary breast and ovarian cancer syndromes; PARP inhibitor therapy
类别
资金
- Myriad Genetics
- Ambry Genetics
- Invitae
The advent of multiple-gene germline panel testing has led to significant advances in hereditary breast and ovarian cancer risk assessment. These include guideline-specific cancer risk management recommendations for patients and their families, such as screening with breast magnetic resonance imaging and risk-reducing surgeries, which have the potential to reduce substantially the morbidity and mortality associated with a hereditary cancer predisposition. However, controversy remains about the clinical validity and actionability of genetic testing in a broader patient population. We discuss events leading to the wider availability of commercialized multiple-gene germline panel testing, the recent data that support using this powerful tool to improve cancer risk assessment and reduction strategies, and remaining challenges to clinical optimization of this new genetic technology.
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