Unit of Urology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Urology and Organ Transplantation, University of Foggia, Foggia, Italy.
World J Urol. 2023 Nov;41(11):2967-2974. doi: 10.1007/s00345-023-04634-2. Epub 2023 Oct 3.
The primary aim of this study was to evaluate if exposure to 5-alpha-reductase inhibitors (5-ARIs) modifies the effect of MRI for the diagnosis of clinically significant Prostate Cancer (csPCa) (ISUP Gleason grade ≥ 2).
This study is a multicenter cohort study including patients undergoing prostate biopsy and MRI at 24 institutions between 2013 and 2022. Multivariable analysis predicting csPCa with an interaction term between 5-ARIs and PIRADS score was performed. Sensitivity, specificity, and negative (NPV) and positive (PPV) predictive values of MRI were compared in treated and untreated patients.
705 patients (9%) were treated with 5-ARIs [median age 69 years, Interquartile range (IQR): 65, 73; median PSA 6.3 ng/ml, IQR 4.0, 9.0; median prostate volume 53 ml, IQR 40, 72] and 6913 were 5-ARIs naïve (age 66 years, IQR 60, 71; PSA 6.5 ng/ml, IQR 4.8, 9.0; prostate volume 50 ml, IQR 37, 65). MRI showed PIRADS 1-2, 3, 4, and 5 lesions in 141 (20%), 158 (22%), 258 (37%), and 148 (21%) patients treated with 5-ARIs, and 878 (13%), 1764 (25%), 2948 (43%), and 1323 (19%) of untreated patients (p < 0.0001). No difference was found in csPCa detection rates, but diagnosis of high-grade PCa (ISUP GG ≥ 3) was higher in treated patients (23% vs 19%, p = 0.013). We did not find any evidence of interaction between PIRADS score and 5-ARIs exposure in predicting csPCa. Sensitivity, specificity, PPV, and NPV of PIRADS ≥ 3 were 94%, 29%, 46%, and 88% in treated patients and 96%, 18%, 43%, and 88% in untreated patients, respectively.
Exposure to 5-ARIs does not affect the association of PIRADS score with csPCa. Higher rates of high-grade PCa were detected in treated patients, but most were clearly visible on MRI as PIRADS 4 and 5 lesions.
The present study was registered at ClinicalTrials.gov number: NCT05078359.
本研究的主要目的是评估 5-α 还原酶抑制剂(5-ARIs)的暴露是否会改变 MRI 对临床显著前列腺癌(csPCa)(ISUP 分级≥2)的诊断效果。
本研究为多中心队列研究,纳入了 2013 年至 2022 年间 24 家机构行前列腺活检和 MRI 的患者。采用多变量分析,预测有 5-ARIs 和 PIRADS 评分交互作用的 csPCa。比较了治疗组和未治疗组 MRI 的敏感性、特异性、阴性预测值(NPV)和阳性预测值(PPV)。
705 名患者(9%)接受了 5-ARIs 治疗[中位年龄 69 岁,四分位距(IQR):65,73;中位 PSA 6.3ng/ml,IQR 4.0,9.0;中位前列腺体积 53ml,IQR 40,72],6913 名患者未接受 5-ARIs 治疗(年龄 66 岁,IQR 60,71;PSA 6.5ng/ml,IQR 4.8,9.0;前列腺体积 50ml,IQR 37,65)。MRI 显示 PIRADS 1-2、3、4 和 5 病变的患者在接受 5-ARIs 治疗的患者中分别为 141 名(20%)、158 名(22%)、258 名(37%)和 148 名(21%),未接受 5-ARIs 治疗的患者中分别为 878 名(13%)、1764 名(25%)、2948 名(43%)和 1323 名(19%)(p<0.0001)。两组 csPCa 的检出率无差异,但治疗组高级别 PCa(ISUP GG≥3)的检出率较高(23% vs 19%,p=0.013)。我们没有发现 PIRADS 评分和 5-ARIs 暴露之间在预测 csPCa 方面存在交互作用的任何证据。PIRADS≥3 的敏感性、特异性、PPV 和 NPV 在治疗组分别为 94%、29%、46%和 88%,在未治疗组分别为 96%、18%、43%和 88%。
5-ARIs 的暴露不会影响 PIRADS 评分与 csPCa 的相关性。治疗组中检测到的高级别 PCa 比例较高,但大多数在 MRI 上均清晰可见,为 PIRADS 4 和 5 病变。
本研究在 ClinicalTrials.gov 注册号为 NCT05078359。