From the Joint Department of Medical Imaging, University Health Network-Mount Sinai Hospital-Women's College Hospital, University of Toronto, Toronto General Hospital, 585 University Ave, 1PMB-292, Toronto, ON, Canada M5G 2N2 (S.G.); Division of Urology (L.K., M.K.) and Division of Anatomic Pathology, Laboratory Medicine & Molecular Diagnostics (M.R.D.), Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada; Department of Biostatistics, McMaster University, Hamilton, Canada (G.R.P.); Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada (E.C.B.); Department of Pathology and Laboratory Medicine, London Health Sciences Centre, University of Western Ontario, London, Canada (M.M.); and Department of Pathology, Laboratory Medicine Program, University Health Network, University of Toronto, Toronto, Canada (T.H.v.d.K.).
Radiology. 2024 Jul;312(1):e231948. doi: 10.1148/radiol.231948.
Background Intraductal carcinoma (IDC) and invasive cribriform (Cr) subtypes of prostate cancer (PCa) are an indication of aggressiveness, but the evidence regarding whether MRI can be used to detect Cr/IDC-pattern PCa is contradictory. Purpose To compare the detection of Cr/IDC-pattern PCa at multiparametric MRI (mpMRI)-targeted biopsy versus systematic biopsy in biopsy-naive men at risk for PCa. Materials and Methods This study was a secondary analysis of a prospective randomized controlled trial that recruited participants with a clinical suspicion of PCa between April 2017 and November 2019 at five centers. Participants were randomized 1:1 to either the MRI arm or the systematic biopsy arm. Targeted biopsy was performed in participants with a Prostate Imaging Reporting and Data System score of at least 3. MRI features were recorded, and biopsy slides and prostatectomy specimens were reviewed for the presence or absence of Cr/IDC histologic patterns. Comparison of Cr/IDC patterns was performed using generalized linear mixed modeling. Results A total of 453 participants were enrolled, with 226 in the systematic biopsy arm (median age, 65 years [IQR, 59-70 years]; 196 biopsies available for assessment) and 227 in the mpMRI-targeted biopsy arm (median age, 67 years [IQR, 60-72 years]; 132 biopsies available for assessment). Identification of Cr/IDC PCa was lower in the systematic biopsy arm compared with the mpMRI arm (31 of 196 biopsies [16%] vs 33 of 132 biopsies [25%]; = .01). No evidence of a difference in mean cancer core length (CCL) (11.3 mm ± 4.4 vs 9.7 mm ± 4.5; = .09), apparent diffusion coefficient (685 µm/sec ± 178 vs 746 µm/sec ± 245; = .52), or dynamic contrast-enhanced positivity (27 [82%] vs 37 [90%]; = .33) for clinically significant PCa (csPCa) was observed between participants with or without Cr/IDC disease in the MRI arm. Cr/IDC-positive histologic patterns overall had a higher mean CCL compared with Cr/IDC-negative csPCa (11.1 mm ± 4.4 vs 9.2 mm ± 4.1; = .009). Conclusion MRI-targeted biopsy showed increased detection of Cr/IDC histologic patterns compared with systematic biopsy. Clinical trial registration no. NCT02936258 © RSNA, 2024 See also the editorial by Scialpi and Martorana in this issue.
背景 前列腺癌(PCa)的导管内癌(IDC)和浸润性筛状(Cr)亚型是侵袭性的标志,但关于 MRI 是否可用于检测 Cr/IDC 型 PCa 的证据存在矛盾。目的 比较多参数 MRI(mpMRI)靶向活检与系统活检在有 PCa 风险的初诊男性中对 Cr/IDC 型 PCa 的检出情况。材料与方法 本研究是一项前瞻性随机对照试验的二次分析,该试验于 2017 年 4 月至 2019 年 11 月在五个中心招募了有 PCa 临床疑似症状的患者。参与者按 1:1 随机分为 MRI 组或系统活检组。在前列腺影像报告和数据系统评分至少为 3 的患者中进行靶向活检。记录 MRI 特征,并对活检切片和前列腺切除术标本进行评估,以确定是否存在 Cr/IDC 组织学模式。使用广义线性混合模型比较 Cr/IDC 模式。结果 共纳入 453 名参与者,系统活检组 226 名(中位年龄 65 岁[IQR,59-70 岁];可评估的活检标本 196 份),mpMRI 靶向活检组 227 名(中位年龄 67 岁[IQR,60-72 岁];可评估的活检标本 132 份)。与系统活检组相比,mpMRI 组中 Cr/IDC 型 PCa 的检出率较低(196 份活检中有 31 份[16%],132 份活检中有 33 份[25%]; =.01)。在有临床意义的 PCa(csPCa)的患者中,平均癌核心长度(CCL)(11.3 mm ± 4.4 比 9.7 mm ± 4.5; =.09)、表观扩散系数(685 µm/sec ± 178 比 746 µm/sec ± 245; =.52)或动态对比增强阳性率(27 [82%]比 37 [90%]; =.33)方面,未见差异。mpMRI 组中,Cr/IDC 阳性组织学模式的平均 CCL 高于 Cr/IDC 阴性 csPCa(11.1 mm ± 4.4 比 9.2 mm ± 4.1; =.009)。结论 与系统活检相比,mpMRI 靶向活检可提高 Cr/IDC 组织学模式的检出率。临床试验注册号 NCT02936258 © RSNA,2024 参见本期 Scialpi 和 Martorana 的社论。