dc.creator | Lerman, Caryn | en |
dc.creator | Narod, Steven | en |
dc.creator | Schulman, Kevin | en |
dc.creator | Hughes, Chanita | en |
dc.creator | Gomez-Caminero, Andres | en |
dc.creator | Bonney, George | en |
dc.creator | Gold, Karen | en |
dc.creator | Trock, Bruce | en |
dc.creator | Main, David | en |
dc.creator | Lynch, Jane | en |
dc.creator | Fulmore, Cecil | en |
dc.creator | Snyder, Carrie | en |
dc.creator | Lemon, Stephen J. | en |
dc.creator | Conway, Theresa | en |
dc.creator | Tonin, Patricia | en |
dc.creator | Lenoir, Gilbert | en |
dc.creator | Lynch, Henry | en |
dc.date.accessioned | 2015-05-05T19:01:01Z | en |
dc.date.available | 2015-05-05T19:01:01Z | en |
dc.date.created | 1996-06-26 | en |
dc.date.issued | 1996-06-26 | en |
dc.identifier | 10.1001/jama.1996.03530480027036 | en |
dc.identifier.bibliographicCitation | JAMA. 1996 Jun 26; 275(24): 1885-1892. | en |
dc.identifier.issn | 0098-7484 | en |
dc.identifier.uri | http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=&title=JAMA.++&volume=275&issue=24&pages=1885-1892&date=1996&au=Lerman,+Caryn | en |
dc.identifier.uri | http://dx.doi.org/10.1001/jama.1996.03530480027036 | en |
dc.identifier.uri | http://hdl.handle.net/10822/751966 | en |
dc.description.abstract | OBJECTIVES: To identify predictors of utilization of breast-ovarian
cancer susceptibility (BRCA1 gene) testing and to evaluate outcomes of
participation in a testing program. DESIGN: Prospective cohort study with
baseline interview assessment of predictor variables (eg, sociodemographic
factors, knowledge about hereditary cancer and genetic testing, perceptions of
testing benefits, limitations, and risks). BRCA1 test results were offered
after an education and counseling session in a research setting. Outcome
variables (including depression, functional health status, and prophylactic
surgery plans [follow-up only]) were assessed at baseline and 1-month
follow-up interviews. PARTICIPANTS: Adult male and female members (n=279) of
families with BRCA1-linked hereditary breast-ovarian cancer (HBOC). RESULTS:
Of subjects who completed a baseline interview (n=192), 60% requested BRCA1
test results (43% of all study subjects requested results). Requests for
results were more frequent for persons with health insurance (odds ration
[OR], 3.74; 95% confidence interval [CI], 2.06-6.80); more first-degree
relatives affected with breast cancer (OR, 1.59; 95% CI, 1.16-2.16); more
knowledge about BRCA1 testing (OR, 1.85; 95% CI, 1.36-2.50); and indicating
that test benefits are important (OR, 1.45; 95% CI, 1.13-1.86). At follow-up,
noncarriers of BRCA1 mutations showed statistically significant reductions in
depressive symptoms and functional impairment compared with carriers and
nontested individuals. Individuals identified as mutation carriers did not
exhibit increases in depression and functional impairment. Among unaffected
women with no prior prophylactic surgery, 17% of carriers (2/12) intended to
have mastectomies and 33% (4/12) to have oophorectomies. CONCLUSIONS: Only a
subset of HBOC family members are likely to request BRCA1 testing when
available. Rates of test use may be higher in persons of a higher
socioeconomic status and those with more relatives affected with breast
cancer. For some high-risk individuals who receive test results in a research
setting that includes counseling, there may be psychological benefits. More
research is needed to assess the generalizability of these results and
evaluate the long-term consequences of BRCA1 testing. | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:MEDKIE/96256342 | en |
dc.subject | Attitudes | en |
dc.subject | Breast Cancer | en |
dc.subject | Cancer | en |
dc.subject | Counseling | en |
dc.subject | Carriers | en |
dc.subject | Consent | en |
dc.subject | Decision Making | en |
dc.subject | Depressive Disorder | en |
dc.subject | Education | en |
dc.subject | Evaluation | en |
dc.subject | Evaluation Studies | en |
dc.subject | Family Members | en |
dc.subject | Females | en |
dc.subject | Genetic Disorders | en |
dc.subject | Genetic Predisposition | en |
dc.subject | Genetic Testing | en |
dc.subject | Genetic Screening | en |
dc.subject | Health | en |
dc.subject | Health Insurance | en |
dc.subject | Health Status | en |
dc.subject | Informed Consent | en |
dc.subject | Insurance | en |
dc.subject | Interviews | en |
dc.subject | Knowledge | en |
dc.subject | Males | en |
dc.subject | Mutation | en |
dc.subject | Ovarian Cancer | en |
dc.subject | Ovaries | en |
dc.subject | Patients | en |
dc.subject | Research | en |
dc.subject | Risk | en |
dc.subject | Risks and Benefits | en |
dc.subject | Relatives | en |
dc.subject | Surgery | en |
dc.subject | Survey | en |
dc.subject | Uncertainty | en |
dc.title | BRCA1 Testing in Families With Hereditary Breast-Ovarian Cancer: A Prospective Study of Patient Decision Making and Outcomes | en |
dc.provenance | Digital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine. | en |
dc.provenance | Digital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University. | en |