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基于前列腺体积纳入的四个 Kallikrein 面板鉴别能力的个体患者数据分析荟萃分析。

Individual Patient Data Meta-analysis of Discrimination of the Four Kallikrein Panel Associated With the Inclusion of Prostate Volume.

机构信息

Department of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.

Andover Urology, Andover, MA, Tufts University School of Medicine, Boston, MA.

出版信息

Urology. 2021 Nov;157:102-106. doi: 10.1016/j.urology.2021.08.014. Epub 2021 Aug 24.

Abstract

OBJECTIVE

To assess whether adding prostate volume to the kallikrein panel improves discrimination for ISUP Grade Group 2 or higher (GG2+) disease, as some men may have volume measurements available at the time of blood draw. While prostate volume predicts biopsy outcome, it requires an imaging procedure for measurement. The four kallikrein panel - commercially available as the 4Kscore - predicts risk of GG2+ disease and requires only a blood draw.

MATERIALS AND METHODS

A total of 9131 patients with available prostate volume and total PSA ≤25 ng/ml from 5 historical (sextant biopsy, pre-ISUP 2005 grading) and 4 contemporary cohorts (10+ cores, ISUP 2005 grading). Previously published kallikrein panel models were used to predict risk of GG2+. Volume was added to the model in each cohort and change in discrimination was meta-analyzed.

RESULTS

Increased prostate volume was associated with decreased risk of GG2+ disease after controlling for the kallikrein panel in 7/9 cohorts. However, kallikrein panel discrimination (0.817, 95% CI 0.802, 0.831) was not improved after including volume (AUC difference 0.002, 95% CI -0.003, 0.006). Heterogeneity (P <.0001) was driven by an AUC increase in 1 cohort of academic cancer centers (0.044, 95% CI 0.025, 0.064), with no evidence of heterogeneity after excluding this cohort (P = .15).

CONCLUSION

The kallikrein panel provides a non-invasive approach to assess the risk of high-grade prostate cancer. Our results do not justify the inclusion of prostate volume in the four kallikrein panel. There is some evidence that the predictive value of prostate volume is provider dependent: further research is needed to address this question.

摘要

目的

评估在激肽释放酶组基础上增加前列腺体积是否能提高 ISUP 分级组 2 或更高(GG2+)疾病的鉴别能力,因为有些男性在采血时可能有前列腺体积测量值。虽然前列腺体积可预测活检结果,但需要进行影像学检查来测量。目前有一个基于激肽释放酶的四项检测(简称 4Kscore)的商业检测可预测 GG2+疾病的风险,只需采集血液样本。

材料与方法

共有 9131 例患者来自 5 个历史队列(6 针活检,2005 年前 ISUP 分级)和 4 个当代队列(10 针以上活检,2005 年后 ISUP 分级),这些患者的前列腺体积和总 PSA 均≤25ng/ml。使用先前发表的激肽释放酶模型来预测 GG2+风险。在每个队列中,我们将体积添加到模型中,并进行荟萃分析以评估对鉴别力的影响。

结果

在控制了激肽释放酶组后,7/9 个队列的前列腺体积与 GG2+疾病风险呈负相关。然而,纳入体积后激肽释放酶组的鉴别力(0.817,95%CI 0.802,0.831)并未提高(AUC 差值 0.002,95%CI -0.003,0.006)。异质性(P<0.0001)主要是由于一个学术癌症中心队列的 AUC 增加(0.044,95%CI 0.025,0.064),但排除该队列后无异质性(P=0.15)。

结论

激肽释放酶组为评估高级别前列腺癌风险提供了一种非侵入性方法。我们的结果不支持在激肽释放酶组中加入前列腺体积。有一些证据表明前列腺体积的预测价值与提供者有关:需要进一步研究来解决这个问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c08/8671182/1ba97e441dc4/nihms-1735472-f0001.jpg

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