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乳腺癌初次治疗期间参与遗传咨询和BRCA检测的障碍。

Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer.

作者信息

Schlich-Bakker Kathryn J, ten Kroode Herman F J, Wárlám-Rodenhuis Carla C, van den Bout Jan, Ausems Margreet G E M

机构信息

Department of Medical Oncology, University Medical Center, Utrecht, the Netherlands.

出版信息

Genet Med. 2007 Nov;9(11):766-77. doi: 10.1097/gim.0b013e318159a318.

Abstract

PURPOSE

Little is known about reasons why eligible breast cancer patients decline BRCA mutation testing. They may withdraw at different stages during genetic counseling for different reasons. We prospectively studied perceived benefits and barriers to genetic counseling and BRCA testing in 102 newly diagnosed breast cancer patients approached for genetic counseling at the start of radiotherapy.

METHODS

Patients completed questionnaires and participated in interviews at different stages of the counseling protocol.

RESULTS

Participation was not influenced by distress, knowledge about hereditary breast cancer, previous genetic testing in relatives, or perceived risks and barriers. Immediate decliners (n = 23) do not believe genetic testing is relevant for them. Patients who decline after pedigree compilation (n = 14) are more hesitant and anxious about the influence of the test result on their future often wishing to postpone further testing. Late decliners (n = 7) withdraw afraid of the test result and/or after a relative's objection. These decliners are not easily identified upon approach because they are similar to patients who receive a DNA test result (n = 58). Notwithstanding their decline, 81% agreed to the timing or would have preferred an earlier approach for genetic counseling.

CONCLUSION

Decliners may make more informed decisions after tailored health education, including adequate risk information.

摘要

目的

对于符合条件的乳腺癌患者拒绝进行BRCA突变检测的原因,我们知之甚少。他们可能会因不同原因在遗传咨询的不同阶段退出。我们对102例新诊断的乳腺癌患者进行了前瞻性研究,这些患者在放疗开始时前来接受遗传咨询,研究他们对遗传咨询和BRCA检测的感知益处及障碍。

方法

患者在咨询方案的不同阶段完成问卷并参与访谈。

结果

参与情况不受痛苦程度、对遗传性乳腺癌的了解、亲属先前的基因检测或感知到的风险及障碍的影响。立即拒绝者(n = 23)不认为基因检测与他们相关。在编制家系图后拒绝的患者(n = 14)对检测结果对其未来的影响更为犹豫和焦虑,常常希望推迟进一步检测。后期拒绝者(n = 7)因害怕检测结果和/或在亲属反对后退出。这些拒绝者在初次接触时不易被识别,因为他们与接受DNA检测结果的患者(n = 58)相似。尽管他们拒绝了,但81%的人同意了咨询时间,或者原本希望更早接受遗传咨询。

结论

在进行包括充分风险信息在内的针对性健康教育后,拒绝者可能会做出更明智的决定。

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