The Changing Landscape of Genetic Testing for Inherited Breast Cancer Predisposition

被引:20
|
作者
Afghahi, Anosheh [1 ]
Kurian, Allison W. [2 ]
机构
[1] Univ Colorado, Div Oncol, 1665 Aurora Ct,Mailstop F704, Aurora, CO 80045 USA
[2] Stanford Univ, HRP Redwood Bldg,Room T254A 259 Campus Dr, Stanford, CA 94305 USA
关键词
BRCA1/2; ATM; CHEK2; PALB2; Multiple-gene testing; Hereditary breast and ovarian cancer syndromes; PARP inhibitor therapy; DIFFUSE GASTRIC-CANCER; BRCA2 MUTATION CARRIERS; OVARIAN-CANCER; HEREDITARY BREAST; RISK-ASSESSMENT; SUSCEPTIBILITY GENE; GERMLINE MUTATIONS; PHASE-2; TRIAL; FAMILIES; PANEL;
D O I
10.1007/s11864-017-0468-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页数:10
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