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前瞻性研究在临床怀疑患有前列腺癌且未经活检的患者中使用 Select MDx 检测对高级别前列腺癌的诊断准确性。

Prospective study of diagnostic accuracy in the detection of high-grade prostate cancer in biopsy-naïve patients with clinical suspicion of prostate cancer who underwent the Select MDx test.

机构信息

Department of Urology, Institute of Biomedicine of Seville (IBIS), Virgen del Rocio University Hospital (HVR), Seville, Spain.

Department of Urology, Puerta del Mar University Hospital, Cadiz, Spain.

出版信息

Prostate. 2021 Sep;81(12):857-865. doi: 10.1002/pros.24182. Epub 2021 Jun 29.

Abstract

OBJECTIVES

This study aimed to externally validate the diagnostic accuracy of the Select MDx test for Significant prostate cancer (Sig PCa) (ISUP > 1), in a contemporaneous, prospective, multicenter cohort with a prostate-specific antigen (PSA) between 3 and 10 ng/ml and a non-suspicious digital rectal examination.

METHODS AND PARTICIPANTS

For all enrolled patients, the Select Mdx test, the risk calculator ERSPC3 + DRE, and a prostatic magnetic resonance imaging (MRI) were carried out. Subsequently, a systematic 12-core trans-rectal biopsy and a targeted biopsy, in the case of a prostate imaging-reporting and data system (PIRADS) > 2 lesion (max three lesions), were performed. To assess the accuracy of the Select MDx test in the detection of clinically Sig PCa, the test sensitivity was evaluated. Secondary objectives were specificity, negative predictive value (NPV), positive predictive value (PPV), and area under the curve (AUC). A direct comparison with the ERSPC + DRE risk calculator and MRI were also performed. We also studied the predictive ability to diagnose Sig PCa from the combination of the Select MDx test with MRI using clinical decision-curve analysis.

RESULTS

There were 163 patients enrolled after meeting the inclusion criteria and study protocol. The Select MDx test showed a sensitivity of 76.9% (95% CI, 63.2-87.5), 49.6% specificity (95% CI, 39.9-59.2), 82.09% (95% CI, 70.8-90.4) NPV, and 41.67% (95% CI, 31.7-52.2) PPV for the diagnosis of Sig PCa. COR analysis was also performed, which showed an AUC of 0.63 (95% CI, 0.56-0.71). There were no differences in the accuracy of Select MDx, ERSPC + DRE, or MRI. The combination of Select MDX + MRI showed the highest impact in the decision-curve analysis, with an NPV of 93%.

CONCLUSION

Our study showed a worse performance for the SelectMdx test than previously reported, within a cohort of patients with a PSA 3-10 ng/ml and a normal DRE, with results similar to those from ERSPC + DRE RC and MRI, but with an improvement in the usual PSA pathway. A combination of the Select Mdx test and MRI could improve accuracy, but studies specifically evaluating this scenario with a cost-effective analysis are needed.

摘要

目的

本研究旨在对 Select MDx 检测用于诊断前列腺特异性抗原(PSA)在 3 至 10ng/ml 之间且直肠指检无异常的前列腺癌(Sig PCa)(ISUP>1)的准确性进行外部验证。

方法和参与者

对所有入组患者均进行 Select Mdx 检测、ERSPC3+DRE 风险计算器和前列腺磁共振成像(MRI)检查。随后,对前列腺影像报告和数据系统(PIRADS)>2 病变(最多 3 个病变)进行系统的 12 核经直肠活检和靶向活检。为评估 Select MDx 检测在检测临床 Sig PCa 中的准确性,评估了检测的敏感性。次要目标是特异性、阴性预测值(NPV)、阳性预测值(PPV)和曲线下面积(AUC)。还与 ERSPC+DRE 风险计算器和 MRI 进行了直接比较。我们还使用临床决策曲线分析研究了 Select MDx 检测与 MRI 相结合对诊断 Sig PCa 的预测能力。

结果

在满足纳入标准和研究方案后,有 163 名患者入组。Select MDx 检测的敏感性为 76.9%(95%CI,63.2-87.5),特异性为 49.6%(95%CI,39.9-59.2),82.09%(95%CI,70.8-90.4)NPV,41.67%(95%CI,31.7-52.2)PPV 用于诊断 Sig PCa。还进行了 COR 分析,显示 AUC 为 0.63(95%CI,0.56-0.71)。Select MDx、ERSPC+DRE 或 MRI 的准确性没有差异。Select MDX+MRI 的组合在决策曲线分析中显示出最高的影响,NPV 为 93%。

结论

我们的研究表明,在 PSA 为 3-10ng/ml 且直肠指检正常的患者队列中,SelectMdx 检测的性能比之前报道的要差,结果与 ERSPC+DRE RC 和 MRI 相似,但改善了常用的 PSA 检测途径。Select Mdx 检测与 MRI 的组合可能会提高准确性,但需要进行专门针对这种情况进行成本效益分析的研究。

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