VISION:磁共振成像靶向活检与标准经直肠超声引导活检在前列腺癌检测中的个人患者数据随机试验 Meta 分析。

Veeru Kasivisvanathan, Vinson Wai-Shun Chan, Keiran D Clement, Brooke Levis, Alexander Ng, Aqua Asif, Masoom A Haider, Mark Emberton, Gregory R Pond, Ridhi Agarwal, Katie Scandrett, Yemisi Takwoingi, Laurence Klotz, Caroline M Moore
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引用次数: 0

摘要

背景和目的:PRECISION 和 PRECISE 试验比较了磁共振成像靶向活检(MRI ± TB)与标准的经直肠超声(TRUS)引导活检,以检测具有临床意义的前列腺癌(csPCa)。PRECISION证明MRI±TB优于TRUS引导活检,而PRECISE则证明不存在劣效性。VISION 研究是一项计划中的个体患者数据荟萃分析 (IPDMA),比较了 MRI ± TB 与 TRUS 引导下活检对 csPCa 诊断的效果:于 2023 年 11 月 12 日在 MEDLINE、EMBASE、Web of Science、Cochrane Central of Registered Trials 和 ClinicalTrials.gov 上检索了临床怀疑为前列腺癌的活检无效患者接受 MRI 或标准 TRUS 检查的随机对照试验。如果有可疑磁共振成像的参与者仅接受了靶向活检,而无可疑病变的参与者避免了活检,则纳入研究。主要结果是确诊为 csPCa(Gleason ≥3+4)的男性比例:IPDMA纳入了两项研究,即PRECISION和PRECISE(953名患者)。在MRI±TB研究组中,32.2%的患者因MRI不可疑而避免了活检。与 TRUS 活检相比,MRI ± TB 检测出的 csPCa 高出 8.7 个百分点(36.3% vs 27.6%;95% 置信区间 [CI] 2.8-14.6,p = 0.004),比 TRUS 活检高出 12.3 个百分点(9.6% vs 21.9%;95% CI 7.8-16.9,p 结论和临床意义:在检测 csPCa 和避免诊断 cisPCa 方面,MRI ± TB 途径优于 TRUS 活检。应将磁共振成像纳入前列腺癌诊断的标准治疗路径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VISION: An Individual Patient Data Meta-analysis of Randomised Trials Comparing Magnetic Resonance Imaging Targeted Biopsy with Standard Transrectal Ultrasound Guided Biopsy in the Detection of Prostate Cancer.

Background and objective: The PRECISION and PRECISE trials compared magnetic resonance imaging targeted biopsy (MRI ± TB) with the standard transrectal ultrasound (TRUS) guided biopsy for the detection of clinically significant prostate cancer (csPCa). PRECISION demonstrated superiority of MRI ± TB over TRUS guided biopsy, while PRECISE demonstrated noninferiority. The VISION study is a planned individual patient data meta-analysis (IPDMA) comparing MRI ± TB with TRUS guided biopsy for csPCa diagnosis.

Methods: MEDLINE, EMBASE, Web of Science, Cochrane Central of Registered Trials, and ClinicalTrials.gov were searched on the November 12, 2023 for randomised controlled trials of biopsy-naïve patients with a clinical suspicion of prostate cancer undergoing MRI or standard TRUS. Studies were included if its participants with suspicious MRI underwent targeted biopsy alone and those with nonsuspicious lesion avoided biopsy. The primary outcome is the proportion of men diagnosed with csPCa (Gleason ≥3 + 4).

Key findings and limitations: Two studies, PRECISION and PRECISE (953 patients), were included in the IPDMA. In the MRI ± TB arm, 32.2% of patients avoided biopsy due to nonsuspicious MRI. MRI ± TB detected 8.7 percentage points (36.3% vs 27.6%; 95% confidence interval [CI] 2.8-14.6, p = 0.004) more csPCa than TRUS biopsy and 12.3 percentage points (9.6% vs 21.9%; 95% CI 7.8-16.9, p < 0.001) less clinically insignificant prostate cancer (cisPCa; Gleason 3 + 3). The overall risk of bias for the included studies were found to be low after assessment using the QUADAS-2, QUADAS-C, and ROB 2.0 tools.

Conclusions and clinical implications: The MRI ± TB pathway is superior to TRUS biopsy in detecting csPCa and avoiding the diagnosis of cisPCa. MRI should be included in the standard of care pathway for prostate cancer diagnosis.

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