Nicola Schieda, Christopher Morash, Luke T Lavallee, Trevor A Flood, Ilias Cagiannos, Ehab Elzayat, Zoya Patni, Tim Ramsay, Rodney H Breau
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引用次数: 0
Abstract
Objective: To compare clinically significant prostate cancer (CS-PCa) detection by transperineal (TP) compared to transrectal (TR) magnetic resonance imaging (MRI)-ultrasonography (US) fusion prostate biopsy.
Patients and methods: Males with abnormal prostate MRI (one or more lesion[s], Prostate Imaging-Reporting and Data System [PI-RADS] score ≥3) consenting to prostate biopsy were enrolled in a randomised control trial (NCT03936127) performed at single-site tertiary care referral centre from October 2022 to June 2024. The patients were randomised to either TP or TR biopsy approach. The primary outcome was CS-PCa (International Society of Urogenital Pathology Grade Group ≥2). Subgroup analysis of the primary outcome was stratified by lesion location (posterior, anterior; and apex, middle, base) and PI-RADS score. Secondary outcomes were detection of any grade PCa, infection, and patient pain score.
Results: In total, 233 patients were randomised (119 patients with 168 lesions in the TP group and 114 patients with 151 lesions in the TR group). CS-PCa was detected in: 61% (73/119; 95% confidence interval [CI] 52-70%) for TP and 54% (62/114; 95% CI 45-64%) for TR (relative risk [RR] 1.13, 95% CI 0.93-1.38, P = 0.23). Adjusted CS-PCa detection rates were higher for TP in anterior lesions: 29% (95% CI 15-49%) vs 16% (95% CI 7-31%) (RR 1.81, 95% CI 1.05-3.12; P = 0.03) and PI-RADS score 4 lesions: 51% (95% CI 39-62%) vs 30% (95% CI 19-43%) (RR 1.77, 95% CI 1.13-2.76; P = 0.01), with no difference in apical lesions (RR 0.91, 95% CI 0.60-1.37; P = 0.65). The median (interquartile range) pain score was 3 (2-4) in the TP group and 2 (1-5) in the TR group (P = 0.09). There were no urinary tract infections or urosepsis events in either group. No patient was withdrawn due to adverse events.
Conclusions: In this trial, we failed to demonstrate a statistically significant, increase in the detection of CS-PCa using TP compared to TR biopsy. There were no sepsis events and biopsy was tolerated in both patient groups. MRI-US fusion prostate biopsy using a TP approach may be more advantageous for anterior and smaller lesions, higher powered studies are needed.
目的:比较经会阴(TP)与经直肠(TR)磁共振成像(MRI)-超声(US)融合前列腺活检对临床意义重大的前列腺癌(CS-PCa)的检测效果。患者和方法:前列腺MRI异常(一个或多个病变,前列腺成像报告和数据系统评分≥3)的男性同意进行前列腺活检,于2022年10月至2024年6月在单点三级保健转诊中心进行随机对照试验(NCT03936127)。患者随机选择TP或TR活检方法。主要结局为CS-PCa(国际泌尿生殖病理学会分级组≥2)。亚组分析的主要结局是根据病变位置(后方,前方;以及先端、中间、基部)和PI-RADS评分。次要结果是检测到任何级别的PCa、感染和患者疼痛评分。结果:共纳入233例患者(TP组119例,168个病变,TR组114例,151个病变)。CS-PCa检出率:61% (73/119;95%可信区间[CI] 52-70%), 54% (62/114;(相对危险度[RR] 1.13, 95% CI 0.93-1.38, P = 0.23)。前病变中TP的校正CS-PCa检出率更高:29% (95% CI 15-49%) vs 16% (95% CI 7-31%) (RR 1.81, 95% CI 1.05-3.12;P = 0.03), PI-RADS评分4个病变:51% (95% CI 39-62%) vs 30% (95% CI 19-43%) (RR 1.77, 95% CI 1.13-2.76;P = 0.01),根尖病变无差异(RR 0.91, 95% CI 0.60-1.37;p = 0.65)。TP组疼痛评分中位数(四分位间距)为3(2-4)分,TR组为2(1-5)分(P = 0.09)。两组均未发生尿路感染或尿脓毒症事件。没有患者因不良事件而退出。结论:在本试验中,我们未能证明与TR活检相比,TP对CS-PCa的检测有统计学意义的增加。两组患者均无脓毒症发生,活检耐受。采用TP入路的MRI-US融合前列腺活检可能对前路和较小病变更有利,需要更有力的研究。
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