Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/546
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dc.contributor.authorWatts, K. J.en
dc.contributor.authorSpillane, A.en
dc.contributor.authorGregory, P.en
dc.contributor.authorBastick, P.en
dc.contributor.authorBarlow-Stewart, K.en
dc.contributor.authorPeate, M.en
dc.contributor.authorLobb, E. A.en
dc.contributor.authorMatthews, A.en
dc.contributor.authorGrieve, S.en
dc.contributor.authorAndrews, L.en
dc.contributor.authorWhite, M.en
dc.contributor.authorHattam, A.en
dc.contributor.authorMcKay, L.en
dc.contributor.authorMak, C.en
dc.contributor.authorFox, J.en
dc.contributor.authorElder, E.en
dc.contributor.authorHarris, M.en
dc.contributor.authorZia, R.en
dc.contributor.authorEdirimanne, S.en
dc.contributor.authorCrowe, K.en
dc.contributor.authorTucker, K.en
dc.contributor.authorPoliness, C.en
dc.contributor.authorParasyn, A.en
dc.contributor.authorHart, S.en
dc.contributor.authorGeelhoed, L.en
dc.contributor.authorHenderson, M.en
dc.contributor.authorD'Arcy, J.en
dc.contributor.authorField, M.en
dc.contributor.authorKirk, J.en
dc.contributor.authorLipton, L.en
dc.contributor.authorGale, J.en
dc.contributor.authorInder, S.en
dc.contributor.authorCheung, D.en
dc.contributor.authorUng, O.en
dc.contributor.authorFrench, J.en
dc.contributor.authorSaunders, C.en
dc.contributor.authorBowman, M.en
dc.contributor.authorMoore, K.en
dc.contributor.authorSmythe, C.en
dc.contributor.authorKelly, P. J.en
dc.contributor.authorZilliacus, E.en
dc.contributor.authorDickson, R.en
dc.contributor.authorSusman, R.en
dc.contributor.authorDuffy, J.en
dc.contributor.authorMitchell, G.en
dc.contributor.authorEdwards, E.en
dc.contributor.authorMoon, D.en
dc.contributor.authorRahman, B.en
dc.contributor.authorCrowe, P.en
dc.contributor.authorGleeson, M.en
dc.contributor.authorThomson, D.en
dc.contributor.authorMeiser, B.en
dc.contributor.authorNeil, G.en
dc.contributor.authorO'Brien, J.en
dc.contributor.authorLynch, J.en
dc.contributor.authorCreighton, L.en
dc.contributor.authorSecomb, E.en
dc.contributor.authorCicciarelli, L.en
dc.contributor.authorSnook, K.en
dc.contributor.authorSenior, J.en
dc.contributor.authorSchwartz, P.en
dc.contributor.authorAntill, Y.en
dc.contributor.authorHopper, J.en
dc.contributor.authorFriedlander, M.en
dc.date.accessioned2018-06-16T20:35:24Z-
dc.date.available2018-06-16T20:35:24Z-
dc.date.issued2012en
dc.identifier.citation28 Jul 12, (320), 2012en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/546-
dc.description.abstractBackground: Germline BRCA1 and BRCA2 mutation testing offered shortly after a breast cancer diagnosis to inform women's treatment choices - treatment-focused genetic testing 'TFGT' - has entered clinical practice in specialist centers and is likely to be soon commonplace in acute breast cancer management, especially for younger women. Yet the optimal way to deliver information about TFGT to younger women newly diagnosed with breast cancer is not known, particularly for those who were not suspected of having a hereditary breast cancer syndrome prior to their cancer diagnosis. Also, little is known about the behavioral and psychosocial impact or cost effectiveness of educating patients about TFGT. This trial aims to examine the impact and efficiency of two models of educating younger women newly diagnosed with breast cancer about genetic testing in order to provide evidence for a safe and effective future clinical pathway for this service.Design/methods: In this non-inferiority randomized controlled trial, 140 women newly diagnosed with breast cancer (aged less than 50 years) are being recruited from nine cancer centers in Australia. Eligible women with either a significant family history of breast and/or ovarian cancer or with other high risk features suggestive of a mutation detection rate of > 10% are invited by their surgeon prior to mastectomy or radiotherapy. After completing the first questionnaire, participants are randomized to receive either: (a) an educational pamphlet about genetic testing (intervention) or (b) a genetic counseling appointment at a family cancer center (standard care). Each participant is offered genetic testing for germline BRCA mutations. Decision-related and psychosocial outcomes are assessed over 12 months and include decisional conflict (primary outcome);uptake of bilateral mastectomy and/or risk-reducing salpingo-oophorectomy; cancer-specific- and general distress; family involvement in decision making; and decision regret. A process-oriented retrospective online survey will examine health professionals' attitudes toward TFGT; a health economic analysis will determine the cost effectiveness of the intervention.Discussion: This trial will provide crucial information about the impact, efficiency and cost effectiveness of an educational pamphlet designed to inform younger women newly diagnosed with breast cancer about genetic testing. Issues regarding implementation of the trial are discussed.Trial registration: The study is registered with the Australian and New Zealand Clinical Trials Group (Registration no: ACTRN12610000502033). 2012 Watts et al.; licensee BioMed Central Ltd.<br />en
dc.languageenen
dc.relation.ispartofBMC Canceren
dc.titleHow should we discuss genetic testing with women newly diagnosed with breast cancer? Design and implementation of a randomized controlled trial of two models of delivering education about treatment-focused genetic testing to younger women newly diagnosed with breast canceren
dc.typeArticleen
dc.identifier.doihttp://dx.doi.org/10.1186/1471-2407-12-320en
dc.subject.keywordsbrca1Breast canceren
dc.subject.keywordsccccBRCA2en
dc.subject.keywordsClinical practiceen
dc.subject.keywordsGenetic testingen
dc.subject.keywordsTreatmenten
dc.subject.keywordsanxietyen
dc.subject.keywordsarticleen
dc.subject.keywordsAustraliaen
dc.subject.keywordscancer radiotherapyen
dc.subject.keywordscost effectiveness analysisen
dc.subject.keywordsdepressionen
dc.subject.keywordsdistress syndromeen
dc.subject.keywordsfamily historyen
dc.subject.keywordsgene mutationen
dc.subject.keywordsgenetic counselingen
dc.subject.keywordsgenetic screeningen
dc.subject.keywordshealth economicsen
dc.subject.keywordshealth personnel attitudeen
dc.subject.keywordsmastectomyen
dc.subject.keywordsmulticenter study (topic)en
dc.subject.keywordsovary canceren
dc.subject.keywordspatient decision makingen
dc.subject.keywordspatient educationen
dc.subject.keywordsquestionnaireen
dc.subject.keywordsrandomized controlled trial (topic)en
dc.subject.keywordssalpingooophorectomyen
dc.subject.keywordstreatment focused genetic testingen
dc.subject.keywordstumor suppressor geneen
dc.relation.urlhttp://www.biomedcentral.com/1471-2407/12/320http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=emed10&AN=2012612638en
dc.identifier.risid503en
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
Appears in Sites:Queensland Health Publications
Sunshine Coast HHS Publications
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