Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions

被引:98
作者
Murray, Mitzi L. [1 ]
Cerrato, Felecia [1 ]
Bennett, Robin L. [1 ]
Jarvik, Gail P. [1 ]
机构
[1] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
BRCA; genetic variant; surgical decisions; follow-up; genetic counseling; RISK-REDUCING SURGERY; OVARIAN-CANCER; CLINICAL CHARACTERISTICS; PROPHYLACTIC SURGERY; SALPINGO-OOPHORECTOMY; GERMLINE MUTATIONS; PREVENTIVE SURGERY; FAMILY-HISTORY; WOMEN; BREAST;
D O I
10.1097/GIM.0b013e318226fc15
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Approximately 5-10% of patients who undergo genetic testing of BRCA1 and BRCA2 receive a variant of unknown significance (VUS) result. The ambiguous nature of a VUS may increase difficulty in patient understanding and decision making regarding risk reduction and surveillance options, including cancer risk-reducing surgeries. VUS reclassification to benign or deleterious may occur in time; however, clinical decisions may need to be made expeditiously, and some patients may pursue irreversible treatments before VUS reclassification. Methods: We reviewed the surgical decisions of 107 women postdisclosure of a BRCA VUS result counseled at our institute between 1998 and 2009. Conclusion: Among women receiving a BRCA VUS result at our center, 11 of 107 (10.3%) pursued cancer risk-reducing mastectomy and 22 of 107 (20.6%) pursued cancer risk-reducing bilateral salpingooophorectomy. Reclassification of VUS occurred up to 9 years after testing, and 5 of 22 (22.7%) women followed up for 8 or more years continue to have a VUS result. We discuss considerations for providers of genetic services to discuss with patients who receive a VUS result. Genet Med 2011: 13(12): 998-1005.
引用
收藏
页码:998 / 1005
页数:8
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