首页> 外文期刊>BMC Cancer >How 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 cancer
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How 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 cancer

机译:我们应该如何与新诊断出乳腺癌的女性讨论基因检测?两种模式的随机对照试验的设计和实施,以两种模式向新诊断出乳腺癌的年轻女性进行以治疗为重点的基因检测教育

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Background 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)
机译:背景生殖道BRCA1和BRCA2突变测试在乳腺癌诊断后不久就提供,以告知女性治疗选择-以治疗为重点的基因测试'TFGT'-已在专业中心进入临床实践,并且可能很快会在急性乳腺癌管理中变得司空见惯,尤其是对于年轻女性。然而,尚不清楚向新诊断出患有乳腺癌的年轻女性传递有关TFGT信息的最佳方法,尤其是对于那些在癌症诊断之前没有被怀疑患有遗传性乳腺癌综合征的女性。同样,对患者进行TFGT教育的行为和心理影响或成本效益知之甚少。这项试验的目的是检验两种模式的教育模式,这些模式对新诊断出患有乳腺癌的年轻女性进行基因检测,以为该服务的安全有效的未来临床途径提供证据。设计/方法在这项非自卑性随机对照试验中,从澳大利亚的9个癌症中心招募了140名刚被诊断出患有乳腺癌(年龄小于50岁)的女性。乳房切除术或放疗前,由外科医生邀请有显着乳腺癌和/或卵巢癌家族史或其他高风险特征提示突变检出率≥10%的合格妇女。在完成第一份调查表后,参与者将被随机分配以接受:(a)关于基因检测(干预)的教育手册,或(b)在家庭癌症中心接受基因咨询的服务(标准护理)。向每个参与者提供种系BRCA突变的基因测试。在12个月内评估与决策相关的和社会心理结果,包括决策冲突(主要结果);双侧乳房切除术和/或降低风险的输卵管卵巢切除术;特定于癌症的和普遍的困扰;家庭参与决策;和决定感到遗憾。面向过程的回顾性在线调查将检查卫生专业人员对TFGT的态度;健康经济分析将确定干预措施的成本效益。讨论该试验将提供有关教育手册的影响,效率和成本效益的重要信息,该手册旨在为刚被诊断出患有乳腺癌的年轻女性提供基因检测的信息。讨论了有关试验实施的问题。试验注册本研究已在澳大利亚和新西兰临床试验组注册(注册号:ACTRN12610000502033)

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