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Targeted MRI-guided prostate biopsies for the detection of prostate cancer: Initial clinical experience with real-time 3-dimensional transrectal ultrasound guidance and magnetic resonance/transrectal ultrasound image fusion

机译:靶向MRI引导的前列腺活检以检测前列腺癌:实时3维经直肠超声引导和磁共振/经超声图像融合的初步临床经验

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Objective: To prove the feasibility and evaluate the initial clinical results of targeted prostate biopsies using the Urostation novel platform using magnetic resonance imaging (MRI)/transrectal ultrasound (TRUS) registration to help steer the biopsy needle to suspicious areas. Methods: We prospectively included 30 patients for suspicion of prostate cancer from November 2011 to August 2012. All patients were previously evaluated by a multiparametric MRI, interpreted by a single radiologist who attributed a Prostate Imaging-Reporting and Data System (PI-RADS) score to each lesion. A conventional 12-core randomized biopsy protocol was performed and 2 additional targeted biopsies were performed on suspicious area(s). The results of randomized and targeted biopsies were compared. Results: Among the 30 patients, suspicious area(s) were found on MRI in 20 cases (67%). Median procedure time was 23 minutes. Targeting success rate (biopsy visualized inside the target) was 83%, with at least 1 biopsy reaching the target in all cases. Prostate cancer was detected in 14 cases (47%), including 11 cases with an abnormal MRI. Targeted biopsies detected cancer in all 11 cases and all but 1 were clinically significant. Randomized biopsies detected 10 of these 11 cases, and 3 more cases that MRI considered normal. Sensitivity to detect a significant cancer was 91% in both modalities. Conclusion: This initial clinical study showed encouraging results for targeted MRI-guided prostate biopsies using MRI-TRUS fusion. Although further studies are needed to determine the role of prostate MRI before biopsy and the relevance of targeted biopsies, the Urostation is an MRI-TRUS fusion device that has good accuracy for targeting suspicious areas on MRI.
机译:目的:通过使用核磁共振成像(MRI)/经直肠超声(TRUS)配准的Urostation新型平台来证明靶向前列腺活检的可行性,并评估其初始临床结果,以帮助将活检针引导至可疑区域。方法:我们从2011年11月至2012年8月前瞻性纳入了30例怀疑患有前列腺癌的患者。所有患者先前均通过多参数MRI进行了评估,并由一名放射科医生进行了解释,并归因于前列腺成像报告和数据系统(PI-RADS)评分每个病灶。进行了常规的12核随机活检方案,并对可疑区域进行了2次其他靶向活检。比较了随机和靶向活检的结果。结果:30例患者中,有20例(67%)在MRI上发现可疑区域。中位手术时间为23分钟。靶向成功率(活检可见于靶标内部)为83%,在所有情况下至少有1例活检达到了靶标。前列腺癌检出14例(47%),包括11例MRI异常。靶向活检在所有11例病例中均检测出癌症,除1例以外,其他均具有临床意义。随机活检发现这11例病例中有10例,而MRI认为正常的则有3例。在两种方式中,检测到重大癌症的敏感性均为91%。结论:这项初始临床研究显示了使用MRI-TRUS融合技术进行靶向MRI引导的前列腺活检的令人鼓舞的结果。尽管需要进一步的研究来确定活检之前前列腺MRI的作用以及靶向活检的相关性,但Urostation是一种MRI-TRUS融合设备,具有针对MRI上可疑区域的良好准确性。

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