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随机试验发现,前列腺癌遗传风险评分反馈针对高危男性进行前列腺特异性抗原筛查。

Randomized trial finds that prostate cancer genetic risk score feedback targets prostate-specific antigen screening among at-risk men.

作者信息

Turner Aubrey R, Lane Brian R, Rogers Dan, Lipkus Isaac, Weaver Kathryn, Danhauer Suzanne C, Zhang Zheng, Hsu Fang-Chi, Noyes Sabrina L, Adams Tamara, Toriello Helga, Monroe Thomas, McKanna Trudy, Young Tracey, Rodarmer Ryan, Kahnoski Richard J, Tourojman Mouafak, Kader A Karim, Zheng S Lilly, Baer William, Xu Jianfeng

机构信息

Center for Cancer Genomics, Wake Forest School of Medicine, Winston-Salem, North Carolina.

Spectrum Health Hospital System, Grand Rapids, Michigan.

出版信息

Cancer. 2016 Nov 15;122(22):3564-3575. doi: 10.1002/cncr.30162. Epub 2016 Jul 19.

Abstract

BACKGROUND

Prostate-specific antigen (PSA) screening may reduce death due to prostate cancer but leads to the overdiagnosis of many cases of indolent cancer. Targeted use of PSA screening may reduce overdiagnosis. Multimarker genomic testing shows promise for risk assessment and could be used to target PSA screening.

METHODS

To test whether counseling based on the family history (FH) and counseling based on a genetic risk score (GRS) plus FH would differentially affect subsequent PSA screening at 3 months (primary outcome), a randomized trial of FH versus GRS plus FH was conducted with 700 whites aged 40 to 49 years without prior PSA screening. Secondary outcomes included anxiety, recall, physician discussion at 3 months, and PSA screening at 3 years. Pictographs versus numeric presentations of genetic risk were also evaluated.

RESULTS

At 3 months, no significant differences were observed in the rates of PSA screening between the FH arm (2.1%) and the GRS-FH arm (4.5% with GRS-FH vs. 2.1% with FH: χ = 3.13, P = .077); however, PSA screening rates at 3 months significantly increased with given risk in the GRS-FH arm (P = .013). Similar results were observed for discussions with physicians at 3 months and PSA screening at 3 years. Average anxiety levels decreased after the individual cancer risk was provided (P = .0007), with no differences between groups. Visual presentation by pictographs did not significantly alter comprehension or anxiety.

CONCLUSIONS

This is likely the first randomized trial of multimarker genomic testing to report genomic targeting of cancer screening. This study found little evidence of concern about excess anxiety or overuse/underuse of PSA screening when multimarker genetic risks were provided to patients. Cancer 2016;122:3564-3575. © 2016 American Cancer Society.

摘要

背景

前列腺特异性抗原(PSA)筛查可能降低前列腺癌导致的死亡,但会导致许多惰性癌病例被过度诊断。有针对性地使用PSA筛查可能会减少过度诊断。多标记基因组检测在风险评估方面显示出前景,可用于确定PSA筛查的对象。

方法

为了测试基于家族史(FH)的咨询以及基于遗传风险评分(GRS)加FH的咨询是否会对3个月时后续的PSA筛查产生不同影响(主要结局),对700名年龄在40至49岁、未进行过PSA筛查的白人进行了一项FH与GRS加FH的随机试验。次要结局包括焦虑、回忆、3个月时与医生的讨论以及3年时的PSA筛查。还评估了遗传风险的象形图与数字呈现方式。

结果

在3个月时,FH组(2.1%)和GRS - FH组(GRS - FH组为4.5%,FH组为2.1%:χ = 3.13,P = 0.077)的PSA筛查率无显著差异;然而,在GRS - FH组中,3个月时的PSA筛查率随给定风险显著增加(P = 0.013)。在3个月时与医生的讨论以及3年时的PSA筛查中也观察到了类似结果。提供个体癌症风险后,平均焦虑水平下降(P = 0.0007),组间无差异。象形图的视觉呈现方式并未显著改变理解或焦虑程度。

结论

这可能是第一项报告癌症筛查基因组靶向的多标记基因组检测随机试验。本研究发现,当向患者提供多标记遗传风险时,几乎没有证据表明存在对过度焦虑或PSA筛查过度使用/使用不足的担忧。《癌症》2016年;122:3564 - 3575。©2016美国癌症协会。

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本文引用的文献

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Landmarks in prostate cancer screening.前列腺癌筛查的里程碑。
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