精准优先:宾夕法尼亚州泌尿科区域协作组织使用 mri 引导融合针活检检测前列腺癌。

IF 1.5 Q3 UROLOGY & NEPHROLOGY
American journal of clinical and experimental urology Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.62347/BPCP1813
Dennis Head, Ako A Ako, Serge Ginzburg, Eric Singer, Bruce Jacobs, Claudette Fonshell, Adam Reese, Edouard Trabulsi, Jeffrey Tomaszewski, John Danella, Laurence Belkoff, Robert Uzzo, Jay D Raman
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引用次数: 0

摘要

目的:在美国,越来越多的泌尿科医生,包括宾夕法尼亚州泌尿科区域协作组织(Pennsylvania Urologic Regional Collaborative)的泌尿科医生开展了有针对性的前列腺活检,该协作组织是一个由医生主导的数据共享和质量改进协作组织。为了评估合作组织中核磁共振成像引导下的融合针前列腺活检的效果,我们分析了不同临床实践中具有临床意义的前列腺癌检出率的差异,以及与具有临床意义的前列腺癌检出率相关的患者特征:我们分析了 2015 年至 2019 年期间在五家医疗机构进行的 857 例首次 MRI 融合活检手术(至少 20 例)。我们对患者基线特征和分级组(GG)≥ 3 的肿瘤检出率进行了卡方分析。在调整患者基线特征后,我们使用多变量逻辑回归估算了具有临床意义的癌症检出几率:在接受磁共振成像引导的靶向活检的男性中,约有15%的患者年龄小于59岁。前列腺特异性抗原(PSA)中位数为 6.8 纳克/毫升。各医疗机构的 GG ≥ 3 肿瘤检出率从 14.3% 到 28.3% 不等(P = 0.02)。然而,在对临床和放射学因素进行调整后,GG ≥ 3 肿瘤的检出率在不同医疗机构之间并无显著差异。总体而言,GG≥3肿瘤的检出几率增加与年龄增加、DRE异常、PSA升高、腺体体积变小和PI-RADS≥4 MRI病变有关。PI-RADS≥4与Gleason分级≥3前列腺癌的吻合率为81%:我们证明了活检前磁共振成像的价值,因为可疑病变的存在与磁共振成像靶向活检发现有临床意义的前列腺癌之间有很高的一致性。不同临床实践中患者基线特征的差异可能是导致临床重大癌症检出率差异的原因。这些发现有助于合作组织内部的标准化和质量改进工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prioritizing precision: detection of prostate cancer using mri guided fusion needle biopsy across the pennsylvania urologic regional collaborative.

Purpose: Targeted prostate biopsies are increasingly being performed by urologists in the United States including those in the Pennsylvania Urologic Regional Collaborative, a physician-led data-sharing and quality improvement collaborative. To evaluate the performance of MRI guided fusion needle prostate biopsies in the collaborative, we analyzed the variability by practice in rates of detection of clinically significant prostate cancer and patient characteristics associated with detection of clinically significant prostate cancer.

Methods: We analyzed 857 first-time MRI fusion biopsy procedures performed at five practices (minimum 20 procedures) between 2015 and 2019. We used chi-square analysis for baseline patient characteristics and Grade Group (GG) ≥ 3 tumor detection rates by practice. Multivariable logistic regression was used to estimate the odds of clinically significant cancer detection when adjusting for baseline patient characteristics.

Results: Approximately 15% of men undergoing targeted MRI guided biopsy were ≤ 59 years old. Median prostate specific antigen (PSA) was 6.8 ng/ml. Detection rates for GG ≥ 3 tumors ranged from 14.3% to 28.3% (P = 0.02) across practices. However, the odds of GG ≥ 3 tumor detection did not differ significantly between practices after adjusting for clinical and radiographic factors. Overall, increased likelihood of detecting a GG ≥ 3 tumor was associated with increased age, DRE abnormalities, higher PSA, smaller gland volume and PI-RADS ≥ 4 MRI lesions. There was an 81% concordance rate between PI-RADS ≥ 4 and Gleason grade ≥ 3 prostate cancer.

Conclusion: We demonstrate the value of obtaining pre-biopsy MRI given high concordance between presence of suspicious lesions and MRI-targeted biopsy detection of clinically significant prostate cancer. Variability of baseline patient characteristics among practices may account for the observed differences in clinically significant cancer detection rates. These findings can aid standardization and quality improvement efforts within the collaborative.

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