BRCA testing in unaffected young women in the United States, 2006-2017

被引:14
作者
Guo, Fangjian [1 ,2 ]
Scholl, Matthew [3 ]
Fuchs, Erika L. [1 ,2 ]
Berenson, Abbey B. [1 ,2 ]
Kuo, Yong-Fang [2 ,4 ,5 ]
机构
[1] Univ Texas Med Branch, Dept Obstet & Gynecol, 301 Univ Blvd, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Ctr Interdisciplinary Res Womens Hlth, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Sch Med, Galveston, TX 77555 USA
[4] Univ Texas Med Branch, Dept Prevent Med & Community Hlth, Off Biostat, Galveston, TX 77555 USA
[5] Univ Texas Med Branch, Inst Translat Sci, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
BRCA testing; breast cancer; mutation carrier; ovarian cancer; pathogenic variant carrier; primary prevention; unaffected; CONTRALATERAL BREAST-CANCER; RISK-ASSESSMENT; OVARIAN-CANCER; MUTATION CARRIERS; AMERICAN SOCIETY; GENETIC SERVICES; FAMILY-HISTORY; MANAGEMENT; US; PREDISPOSITION;
D O I
10.1002/cncr.32536
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The discovery of the BRCA gene in the 1990s created an opportunity for individualized cancer prevention. BRCA testing in young women before cancer onset enables early detection of those with an increased cancer risk and creates an opportunity to offer lifesaving prophylactic procedures and medications. This study assessed trends in BRCA testing in women younger than 40 years without diagnosed breast or ovarian cancer (unaffected young women [UYW]) for cancer prevention between 2006 and 2017 in the United States. Methods This study included 93,278 adult women 18 to 65 years old with insurance claims for BRCA testing between 2006 and 2017 from the de-identified Optum Clinformatics Data Mart database. The data contained medical claims and administrative information from privately insured individuals in the United States. The proportion of BRCA testing in UYW younger than 40 years among adult women aged 18 to 65 years who received BRCA testing was assessed. Results In 2006, only 10.5% of the tests were performed in UYW. The proportion of BRCA tests performed in UYW increased significantly to 25.5% in 2017 (annual percentage change for the 2006-2017 period, 6.9; 95% confidence interval, 6.4-7.3; P < .001). The increased trend in the proportion of BRCA tests in UYW significantly differed by region of residence and family history of breast or ovarian cancer. Conclusions Over the past decade, there was increased use of BRCA testing for cancer prevention. Additional efforts are needed to maximize the early detection of women with BRCA pathogenic variants so that these cancers may be prevented.
引用
收藏
页码:337 / 343
页数:7
相关论文
共 43 条
  • [1] BRCA Mutation Frequency and Patterns of Treatment Response in BRCA Mutation-Positive Women With Ovarian Cancer: A Report From the Australian Ovarian Cancer Study Group
    Alsop, Kathryn
    Fereday, Sian
    Meldrum, Cliff
    deFazio, Anna
    Emmanuel, Catherine
    George, Joshy
    Dobrovic, Alexander
    Birrer, Michael J.
    Webb, Penelope M.
    Stewart, Colin
    Friedlander, Michael
    Fox, Stephen
    Bowtell, David
    Mitchell, Gillian
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (21) : 2654 - 2663
  • [2] [Anonymous], 2018, NCCN Clinical Practice Guidelines in Oncology
  • [3] [Anonymous], 2020, NCCN Clinical Practice Guidelines in Oncology: Survivorship
  • [4] [Anonymous], 2015, Breast Cancer Facts and Figures 2015-2016
  • [5] Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies
    Antoniou, A
    Pharoah, PDP
    Narod, S
    Risch, HA
    Eyfjord, JE
    Hopper, JL
    Loman, N
    Olsson, H
    Johannsson, O
    Borg, Å
    Pasini, B
    Radice, P
    Manoukian, S
    Eccles, DM
    Tang, N
    Olah, E
    Anton-Culver, H
    Warner, E
    Lubinski, J
    Gronwald, J
    Gorski, B
    Tulinius, H
    Thorlacius, S
    Eerola, H
    Nevanlinna, H
    Syrjäkoski, K
    Kallioniemi, OP
    Thompson, D
    Evans, C
    Peto, J
    Lalloo, F
    Evans, DG
    Easton, DF
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) : 1117 - 1130
  • [6] Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
    Beitsch, Peter D.
    Whitworth, Pat W.
    Hughes, Kevin
    Patel, Rakesh
    Rosen, Barry
    Compagnoni, Gia
    Baron, Paul
    Simmons, Rache
    Smith, Linda Ann
    Grady, Ian
    Kinney, Michael
    Coomer, Cynara
    Barbosa, Karen
    Holmes, Dennis R.
    Brown, Eric
    Gold, Linsey
    Clark, Patricia
    Riley, Lee
    Lyons, Samuel
    Ruiz, Antonio
    Kahn, Sadia
    MacDonald, Heather
    Curcio, Lisa
    Hardwick, Mary Kay
    Yang, Shan
    Esplin, Ed D.
    Nussbaum, Robert L.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (06) : 453 - +
  • [7] Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease
    Beral, V
    Bull, D
    Doll, R
    Peto, R
    Reeves, G
    [J]. LANCET, 2001, 358 (9291) : 1389 - 1399
  • [8] Centers for Disease Control and Prevention (CDC), 2004, MMWR Morb Mortal Wkly Rep, V53, P603
  • [9] Meta-analysis of BRCA1 and BRCA2 penetrance
    Chen, Sining
    Parmigiani, Giovanni
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (11) : 1329 - 1333
  • [10] Hereditary Breast and Ovarian Cancer and Other Hereditary Syndromes: Using Technology to Identify Carriers
    Drohan, Brian
    Roche, Constance A.
    Cusack, James C., Jr.
    Hughes, Kevin S.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2012, 19 (06) : 1732 - 1737