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列线图预测前列腺癌意义的开发和内部验证:在前列腺癌低发国家具有临床适用性吗?一项多中心研究。

Development and internal validation of a nomogram predicting significant prostate cancer: Is it clinically applicable in low prevalent prostate cancer countries? A multicenter study.

机构信息

The Cancer Research Chair, Surgery Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Epidemiology Department, High Institute of Public Health, Alexandria University, Alexandria, Egypt.

出版信息

Prostate. 2024 Jan;84(1):56-63. doi: 10.1002/pros.24625. Epub 2023 Sep 27.

DOI:10.1002/pros.24625
PMID:37759243
Abstract

BACKGROUND

Accurately identifying aggressive prostate tumors and studying them as a separate outcome are urgently needed. Nomogram is a predictive tool using an algorithm, it has been widely applied in clinical practice to predict prognosis. We aimed to develop and internally validate a nomogram predicting clinically significant prostate cancer (csPCa).

METHODS

Data were retrieved from the records of the two main hospitals in Riyadh, during the period 2019-2022. Significant variables associated with csPCa cases were used to develop and internally validate a novel nomogram, utilizing the C index, and calibration curves. Decision curve analysis (DCA) was used to assess its clinical utility.

RESULTS

Prostate imaging reporting and data system (PI-RADS), smaller prostate volume, and prostate-specific antigen (PSA) > 10 ng/mL were significantly associated with the risk csPCa, respectively. The model developed by the nomogram showed an excellent accuracy for csPCa discrimination, as indicated by area under the curve (0.83), and calibration curves. DCA showed that our model was superior and surpassed all other models with a larger net benefit for various threshold probabilities. Based on our model, at a probability threshold of 30%, biopsying patients is the equivalent of a strategy that led to an absolute 5% reduction in the number of biopsies without missing any csPCa.

CONCLUSION

The developed nomogram consisting of PI-RAD, total PSA, and prostate volume showed a robust predictive capacity for csPCa before prostate biopsy that may be valuable for clinical judgment to prevent needless biopsy. Yet, the small percentage (5%) of yielded unnecessary biopsies that could be saved by using such a model, cast an important question on its merit and clinical applicability.

摘要

背景

准确识别侵袭性前列腺肿瘤并将其作为一个独立的结果进行研究是迫切需要的。列线图是一种使用算法的预测工具,已广泛应用于临床实践以预测预后。我们旨在开发和内部验证一种预测临床显著前列腺癌(csPCa)的列线图。

方法

数据来自利雅得的两家主要医院的记录,时间为 2019-2022 年。使用与 csPCa 病例相关的显著变量来开发和内部验证一种新的列线图,利用 C 指数和校准曲线。决策曲线分析(DCA)用于评估其临床实用性。

结果

前列腺影像报告和数据系统(PI-RADS)、较小的前列腺体积和前列腺特异性抗原(PSA)>10ng/ml 与 csPCa 的风险显著相关。列线图模型显示出对 csPCa 区分的优异准确性,曲线下面积(0.83)和校准曲线表明了这一点。DCA 显示,我们的模型具有优势,并且在各种阈值概率下都超过了所有其他模型,具有更大的净收益。基于我们的模型,在概率阈值为 30%的情况下,对患者进行活检相当于一种策略,该策略可导致活检次数减少 5%,而不会错过任何 csPCa。

结论

由 PI-RAD、总 PSA 和前列腺体积组成的开发列线图显示出在前列腺活检前预测 csPCa 的强大能力,这可能对临床判断有价值,以防止不必要的活检。然而,使用这样的模型可以节省 5%的不必要活检,这对其优点和临床适用性提出了一个重要的问题。

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