Department of Radiology, Addenbrooke's Hospital and University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Department of Radiology, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Br J Radiol. 2024 Jan 23;97(1153):113-119. doi: 10.1093/bjr/tqad027.
MRI is now established for initial prostate cancer diagnosis; however, there is no standardized pathway to avoid unnecessary biopsy in low-risk patients. Our study aimed to test previously proposed MRI-focussed and risk-adapted biopsy decision models on a real-world dataset.
Single-centre retrospective study performed on 2055 biopsy naïve patients undergoing MRI. Diagnostic pathways included "biopsy all", "MRI-focussed" and two risk-based MRI-directed pathways. Risk thresholds were based on prostate-specific antigen (PSA) density as low (<0.10 ng mL-2), intermediate (0.10-0.15 ng mL-2), high (0.15-0.20 ng mL-2), or very high-risk (>0.20 ng mL-2). The outcome measures included rates of biopsy avoidance, detection of clinically significant prostate cancer (csPCa), missed csPCa, and overdiagnosis of insignificant prostate cancer (iPCa).
Overall cancer rate was 39.9% (819/2055), with csPCa (Grade-Group ≥2) detection of 30.3% (623/2055). In men with a negative MRI (Prostate Imaging-Reporting and Data System, PI-RADS 1-2), the risk of cancer was 1.2%, 2.6%, 9.0%, and 12.9% in the low, intermediate, high, and very high groups, respectively; for PI-RADS score 3 lesions, the rates were 10.5%, 14.3%, 25.0%, and 33.3%, respectively. MRI-guided pathway and risk-based pathway with a low threshold missed only 1.6% csPCa with a biopsy-avoidance rate of 54.4%, and the risk-based pathway with a higher threshold avoided 62.9% (1292/2055) of biopsies with 2.9% (61/2055) missed csPCa detection. Decision curve analysis found that the "risk-based low threshold" pathway has the highest net benefit for probability thresholds between 3.6% and 13.9%.
Combined MRI and PSA-density risk-based pathways can be a helpful decision-making tool enabling high csPCa detection rates with the benefit of biopsy avoidance and reduced iPCa detection.
This real-world dataset from a large UK-based cohort confirms that combining MRI scoring with PSA density for risk stratification enables safe biopsy avoidance and limits the over-diagnosis of insignificant cancers.
MRI 现已广泛用于前列腺癌的初始诊断;然而,对于低危患者,尚无标准化的路径来避免不必要的活检。本研究旨在对真实世界的数据进行基于 MRI 重点和风险适应的活检决策模型的测试。
对 2055 例初次行 MRI 检查的活检初治患者进行单中心回顾性研究。诊断路径包括“全部活检”、“MRI 重点”和两种基于风险的 MRI 引导活检路径。风险阈值基于前列腺特异性抗原(PSA)密度,低危(<0.10ngmL-2)、中危(0.10-0.15ngmL-2)、高危(0.15-0.20ngmL-2)或极高危(>0.20ngmL-2)。主要结局包括活检避免率、临床显著前列腺癌(csPCa)检出率、漏检 csPCa 率和非显著前列腺癌(iPCa)过度诊断率。
总体癌症检出率为 39.9%(819/2055),csPCa(Gleason 分级≥2)检出率为 30.3%(623/2055)。对于 MRI 阴性(前列腺影像报告和数据系统评分 1-2)的患者,低、中、高和极高危组的癌症风险分别为 1.2%、2.6%、9.0%和 12.9%;对于 MRI 评分 3 分的病变,风险分别为 10.5%、14.3%、25.0%和 33.3%。MRI 引导路径和低风险阈值的基于风险的路径仅漏诊 1.6%的 csPCa,活检避免率为 54.4%;高风险阈值的基于风险的路径避免了 62.9%(1292/2055)的活检,而 csPCa 检出率为 2.9%(61/2055)。决策曲线分析发现,概率阈值在 3.6%至 13.9%之间时,“基于风险的低阈值”路径的净获益最高。
联合 MRI 和 PSA 密度的基于风险的方法可以作为一种有用的决策工具,既能提高 csPCa 的检出率,又能避免活检,减少 iPCa 的检出。
这项来自英国大型队列的真实世界数据证实,结合 MRI 评分和 PSA 密度进行风险分层,可以安全地避免活检,并限制对非显著癌症的过度诊断。