Show simple item record

dc.creatorLerman, Carynen
dc.creatorNarod, Stevenen
dc.creatorSchulman, Kevinen
dc.creatorHughes, Chanitaen
dc.creatorGomez-Caminero, Andresen
dc.creatorBonney, Georgeen
dc.creatorGold, Karenen
dc.creatorTrock, Bruceen
dc.creatorMain, Daviden
dc.creatorLynch, Janeen
dc.creatorFulmore, Cecilen
dc.creatorSnyder, Carrieen
dc.creatorLemon, Stephen J.en
dc.creatorConway, Theresaen
dc.creatorTonin, Patriciaen
dc.creatorLenoir, Gilberten
dc.creatorLynch, Henryen
dc.date.accessioned2015-05-05T19:01:01Zen
dc.date.available2015-05-05T19:01:01Zen
dc.date.created1996-06-26en
dc.date.issued1996-06-26en
dc.identifier10.1001/jama.1996.03530480027036en
dc.identifier.bibliographicCitationJAMA. 1996 Jun 26; 275(24): 1885-1892.en
dc.identifier.issn0098-7484en
dc.identifier.urihttp://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,+Carynen
dc.identifier.urihttp://dx.doi.org/10.1001/jama.1996.03530480027036en
dc.identifier.urihttp://hdl.handle.net/10822/751966en
dc.description.abstractOBJECTIVES: 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.formatArticleen
dc.languageenen
dc.sourceBRL:MEDKIE/96256342en
dc.subjectAttitudesen
dc.subjectBreast Canceren
dc.subjectCanceren
dc.subjectCounselingen
dc.subjectCarriersen
dc.subjectConsenten
dc.subjectDecision Makingen
dc.subjectDepressive Disorderen
dc.subjectEducationen
dc.subjectEvaluationen
dc.subjectEvaluation Studiesen
dc.subjectFamily Membersen
dc.subjectFemalesen
dc.subjectGenetic Disordersen
dc.subjectGenetic Predispositionen
dc.subjectGenetic Testingen
dc.subjectGenetic Screeningen
dc.subjectHealthen
dc.subjectHealth Insuranceen
dc.subjectHealth Statusen
dc.subjectInformed Consenten
dc.subjectInsuranceen
dc.subjectInterviewsen
dc.subjectKnowledgeen
dc.subjectMalesen
dc.subjectMutationen
dc.subjectOvarian Canceren
dc.subjectOvariesen
dc.subjectPatientsen
dc.subjectResearchen
dc.subjectRisken
dc.subjectRisks and Benefitsen
dc.subjectRelativesen
dc.subjectSurgeryen
dc.subjectSurveyen
dc.subjectUncertaintyen
dc.titleBRCA1 Testing in Families With Hereditary Breast-Ovarian Cancer: A Prospective Study of Patient Decision Making and Outcomesen
dc.provenanceDigital 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.provenanceDigital 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


This item appears in the following Collection(s)

Show simple item record


Georgetown University Seal
©2009—2023 Bioethics Research Library
Box 571212 Washington DC 20057-1212
202.687.3885