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使用数学模型量化前列腺体积、活检芯数量和5α-还原酶抑制剂治疗对前列腺癌检测概率的影响。

Quantifying the impact of prostate volumes, number of biopsy cores and 5alpha-reductase inhibitor therapy on the probability of prostate cancer detection using mathematical modeling.

作者信息

Serfling Robert, Shulman Michael, Thompson G L, Xiao Zhiyao, Benaim Elie, Roehrborn Claus G, Rittmaster Roger

机构信息

Department of Mathematical Sciences, University of Texas at Dallas, Richardson, TX 75083, USA.

出版信息

J Urol. 2007 Jun;177(6):2352-6. doi: 10.1016/j.juro.2007.01.116.

Abstract

PURPOSE

Previous studies demonstrated a negative correlation between prostate volume and biopsy yield. By decreasing prostate volume 5alpha-reductase inhibitors may enhance cancer detection, which may explain the greater detection of high grade tumors in the finasteride arm of the Prostate Cancer Prevention Trial.

MATERIALS AND METHODS

A mathematical model was constructed to analyze the effects of prostate and tumor volumes, and biopsy core number on cancer detection. The effects of the volume reduction observed with finasteride in the Prostate Cancer Prevention Trial were also modeled, as was the potential reduction in tumor volume needed to explain the observed difference in prostate cancer detection. The model was also applied to the Reduction by Dutasteride of Prostate Cancer Events study.

RESULTS

A higher number of biopsies are required to ensure a detection probability of 0.90 or greater in larger glands or with smaller tumors. In the Prostate Cancer Prevention Trial for a tumor volume of 1 cc a 17% increase in the detection rate in the finasteride arm would be predicted if there was no change in tumor volume, likewise the rate would be 11% to 17% for the dutasteride arm of the Reduction by Dutasteride of Prostate Cancer Events study. The calculated reduction in tumor volume needed to explain the difference in cancer detection between the finasteride and placebo arms of the Prostate Cancer Prevention Trial would be 51% to 66%.

CONCLUSIONS

This model provides guidance on the optimal number of biopsy cores that accord with an earlier model. These findings also suggest that, if there were no reduction in tumor volume, 5alpha-reductase inhibitor therapy could lead to excess cancer detection, including high grade tumors.

摘要

目的

既往研究表明前列腺体积与活检阳性率之间呈负相关。通过减小前列腺体积,5α-还原酶抑制剂可能会提高癌症检测率,这或许可以解释前列腺癌预防试验中使用非那雄胺组高级别肿瘤检出率更高的原因。

材料与方法

构建一个数学模型,以分析前列腺体积、肿瘤体积和活检针数对癌症检测的影响。还对前列腺癌预防试验中观察到的非那雄胺导致的体积减小效应进行了建模,以及为解释观察到的前列腺癌检测差异所需的肿瘤体积潜在减小情况。该模型也应用于度他雄胺降低前列腺癌事件研究。

结果

对于更大的腺体或更小的肿瘤,需要更多的活检针数才能确保检测概率达到0.90或更高。在前列腺癌预防试验中,对于体积为1立方厘米的肿瘤,如果肿瘤体积没有变化,预计非那雄胺组的检测率将提高17%,同样,在度他雄胺降低前列腺癌事件研究中,度他雄胺组的检测率将提高11%至17%。为解释前列腺癌预防试验中非那雄胺组与安慰剂组之间癌症检测差异所需的计算得出的肿瘤体积减小量为51%至66%。

结论

该模型为与早期模型一致的活检针最佳数量提供了指导。这些发现还表明,如果肿瘤体积没有减小,5α-还原酶抑制剂治疗可能会导致过度的癌症检测,包括高级别肿瘤。

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