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本文引用的文献

1
Reducing unnecessary biopsy during prostate cancer screening using a four-kallikrein panel: an independent replication.利用四项激肽释放酶panel 减少前列腺癌筛查中的不必要活检:一项独立的复制研究。
J Clin Oncol. 2010 May 20;28(15):2493-8. doi: 10.1200/JCO.2009.24.1968. Epub 2010 Apr 26.
2
Operator is an independent predictor of detecting prostate cancer at transrectal ultrasound guided prostate biopsy.在经直肠超声引导下前列腺穿刺活检中,操作者是检测前列腺癌的独立预测因素。
J Urol. 2009 Dec;182(6):2659-63. doi: 10.1016/j.juro.2009.08.036.
3
Screening and prostate-cancer mortality in a randomized European study.一项欧洲随机研究中的筛查与前列腺癌死亡率
N Engl J Med. 2009 Mar 26;360(13):1320-8. doi: 10.1056/NEJMoa0810084. Epub 2009 Mar 18.
4
The Prostate Cancer Prevention Trial and European Randomized Study of Screening for Prostate Cancer risk calculators indicating a positive prostate biopsy: a comparison.前列腺癌预防试验与欧洲前列腺癌筛查随机研究中前列腺活检呈阳性的风险计算器比较
BJU Int. 2008 Nov;102(9):1068-73. doi: 10.1111/j.1464-410X.2008.07940.x. Epub 2008 Aug 18.
5
A graphical device to represent the outcomes of a logistic regression analysis.一种用于表示逻辑回归分析结果的图形工具。
Prostate. 2008 Nov 1;68(15):1674-80. doi: 10.1002/pros.20840.
6
The comparability of models for predicting the risk of a positive prostate biopsy with prostate-specific antigen alone: a systematic review.仅使用前列腺特异性抗原预测前列腺活检阳性风险的模型的可比性:一项系统综述。
Eur Urol. 2008 Aug;54(2):274-90. doi: 10.1016/j.eururo.2008.05.022. Epub 2008 May 22.
7
Negative influence of changing biopsy practice patterns on the predictive value of prostate-specific antigen for cancer detection on prostate biopsy.活检实践模式的改变对前列腺活检中前列腺特异性抗原用于癌症检测的预测价值的负面影响。
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Tyrol Prostate Cancer Demonstration Project: early detection, treatment, outcome, incidence and mortality.蒂罗尔前列腺癌示范项目:早期检测、治疗、结果、发病率和死亡率。
BJU Int. 2008 Apr;101(7):809-16. doi: 10.1111/j.1464-410X.2008.07502.x.
9
Prostate-specific antigen at or before age 50 as a predictor of advanced prostate cancer diagnosed up to 25 years later: a case-control study.50岁及50岁以前的前列腺特异性抗原作为25年后诊断出的晚期前列腺癌的预测指标:一项病例对照研究
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10
Is it necessary to detect all prostate cancers in men with serum PSA levels <3.0 ng/ml? A comparison of biopsy results of PCPT and outcome-related information from ERSPC.对于血清前列腺特异性抗原(PSA)水平<3.0 ng/ml的男性,有必要检测出所有前列腺癌吗?前列腺癌预防试验(PCPT)活检结果与欧洲前列腺癌筛查随机研究(ERSPC)结局相关信息的比较
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前列腺特异性抗原与前列腺癌风险的关系:前列腺活检协作组。

The relationship between prostate-specific antigen and prostate cancer risk: the Prostate Biopsy Collaborative Group.

机构信息

Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

出版信息

Clin Cancer Res. 2010 Sep 1;16(17):4374-81. doi: 10.1158/1078-0432.CCR-10-1328. Epub 2010 Aug 24.

DOI:10.1158/1078-0432.CCR-10-1328
PMID:20736330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2937360/
Abstract

PURPOSE

The relationship between prostate-specific antigen (PSA) level and prostate cancer risk remains subject to fundamental disagreements. We hypothesized that the risk of prostate cancer on biopsy for a given PSA level is affected by identifiable characteristics of the cohort under study.

EXPERIMENTAL DESIGN

We used data from five European and three U.S. cohorts of men undergoing biopsy for prostate cancer; six were population-based studies and two were clinical cohorts. The association between PSA and prostate cancer was calculated separately for each cohort using locally weighted scatterplot smoothing.

RESULTS

The final data set included 25,772 biopsies and 8,503 cancers. There were gross disparities between cohorts with respect to both the prostate cancer risk at a given PSA level and the shape of the risk curve. These disparities were associated with identifiable differences between cohorts: for a given PSA level, a greater number of biopsy cores increased the risk of cancer (odds ratio for >6- versus 6-core biopsy, 1.35; 95% confidence interval, 1.18-1.54; P < 0.0005); recent screening led to a smaller increase in risk per unit change in PSA (P = 0.001 for interaction term) and U.S. cohorts had higher risk than the European cohorts (2.14; 95% confidence interval, 1.99-2.30; P < 0.0005).

CONCLUSIONS

Our results suggest that the relationship between PSA and risk of a positive prostate biopsy varies, both in terms of the probability of prostate cancer at a given PSA value and the shape of the risk curve. This poses challenges to the use of PSA-driven algorithms to determine whether biopsy is indicated.

摘要

目的

前列腺特异性抗原(PSA)水平与前列腺癌风险之间的关系仍存在根本分歧。我们假设,给定 PSA 水平下前列腺癌的活检风险受研究队列的可识别特征的影响。

实验设计

我们使用了五个欧洲和三个美国的前列腺癌活检队列的数据;其中六个是基于人群的研究,两个是临床队列。使用局部加权散点平滑法分别计算每个队列中 PSA 与前列腺癌之间的关联。

结果

最终数据集包括 25772 次活检和 8503 例癌症。在给定 PSA 水平下的前列腺癌风险以及风险曲线的形状方面,各队列之间存在明显差异。这些差异与队列之间可识别的差异有关:对于给定的 PSA 水平,更多的活检芯增加了癌症的风险(6 芯与 >6 芯活检的比值比为 1.35;95%置信区间,1.18-1.54;P<0.0005);最近的筛查导致 PSA 每单位变化的风险增加幅度减小(交互项 P=0.001),并且美国队列的风险高于欧洲队列(2.14;95%置信区间,1.99-2.30;P<0.0005)。

结论

我们的结果表明,PSA 与前列腺活检阳性风险之间的关系存在差异,无论是在给定 PSA 值时前列腺癌的概率方面,还是在风险曲线的形状方面。这给基于 PSA 的算法确定是否进行活检带来了挑战。