Joint Department of Medical Imaging, University of Toronto, University Health Network-Mount Sinai Hospital-Women's College Hospital, Toronto General Hospital (SG), Toronto, Ontario, Canada; Centre de recherche en cancérologie de l'Université Laval, Centre Hospitalier Universitaire de Québec-Pavillon L'Hôtel-Dieu de Québec (VF), Québec, Québec, Canada; Southern Alberta Institute of Urology and Prostate Cancer Centre, University of Calgary (MEH), Calgary, Alberta, Canada; Exact Imaging (TM), Markham, Ontario, Canada; Urology of Virginia (GE), Virginia Beach, Virginia; Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine (CPP), Baltimore, Maryland.
Joint Department of Medical Imaging, University of Toronto, University Health Network-Mount Sinai Hospital-Women's College Hospital, Toronto General Hospital (SG), Toronto, Ontario, Canada; Centre de recherche en cancérologie de l'Université Laval, Centre Hospitalier Universitaire de Québec-Pavillon L'Hôtel-Dieu de Québec (VF), Québec, Québec, Canada; Southern Alberta Institute of Urology and Prostate Cancer Centre, University of Calgary (MEH), Calgary, Alberta, Canada; Exact Imaging (TM), Markham, Ontario, Canada; Urology of Virginia (GE), Virginia Beach, Virginia; Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine (CPP), Baltimore, Maryland.
J Urol. 2016 Aug;196(2):562-9. doi: 10.1016/j.juro.2015.12.093. Epub 2016 Jan 12.
Conventional ultrasound systems operate at 6 to 9 MHz and serve as the standard of care to guide prostate biopsies. We present a protocol using a novel high resolution (29 MHz) transrectal prostate micro-ultrasound system. This protocol includes a scoring system to assess the risk of prostatic carcinoma and enable real-time targeted biopsies.
The ExactVu™ system is currently being used in a multisite, 2,000-patient, randomized clinical trial. Cine loops of 400 biopsies from this trial were used to create the PRI-MUS™ (prostate risk identification using micro-ultrasound) protocol and risk scale. Validation was performed in an independent, pathology blinded set of 100 cines. Three of the 5 investigators performing this validation were familiar with micro-ultrasound but naïve to the PRI-MUS protocol and they received only 1 hour of training.
Each increase in risk score demonstrated a 10.1% increase (95% CI 9.3-10.8) in the probability of clinically significant cancer. The risk score also increased with Gleason sum and cancer length with a slope of 0.15 (95% CI 0.09-0.21) and 0.58 (95% CI 0.43-0.73), respectively. Sensitivity and specificity were 80% and 37%, respectively, and the mean ± SD ROC AUC was 60% ± 2%. The protocol was more accurate for detecting high grade disease (Gleason sum greater than 7) with a peak AUC of 74% (mean 66%).
The new resolution of the micro-ultrasound platform paired with the PRI-MUS protocol shows promise for real-time visualization of suspicious lesions and targeting of biopsies. The improved performance of the protocol in more significant disease is consistent with the focus of the field on decreasing insignificant diagnoses and detecting high risk disease early.
传统超声系统工作频率为 6 至 9MHz,是指导前列腺活检的标准。我们提出了一种使用新型高分辨率(29MHz)经直肠前列腺微超声系统的方案。该方案包括一个评分系统,用于评估前列腺癌的风险,并实现实时靶向活检。
ExactVu™系统目前正在一个多中心、2000 例患者的随机临床试验中使用。从该试验中创建了 PRI-MUS™(使用微超声识别前列腺风险)方案和风险评分,使用了 400 次活检的电影循环。在 100 个电影的独立、病理盲法验证集中进行了验证。进行此验证的 5 名调查员中的 3 名熟悉微超声,但对 PRI-MUS 方案不熟悉,他们仅接受了 1 小时的培训。
风险评分每增加 1 分,临床上显著癌症的概率增加 10.1%(95%CI 9.3-10.8)。风险评分还随着 Gleason 总和癌症长度而增加,斜率分别为 0.15(95%CI 0.09-0.21)和 0.58(95%CI 0.43-0.73)。灵敏度和特异性分别为 80%和 37%,平均±SD ROC AUC 为 60%±2%。该方案在检测高级别疾病(Gleason 总和大于 7)方面更准确,AUC 峰值为 74%(平均 66%)。
微超声平台的新分辨率与 PRI-MUS 方案相结合,有望实现可疑病变的实时可视化和活检靶向。该方案在更严重疾病中的性能提高与该领域的重点一致,即减少无意义的诊断并尽早发现高危疾病。