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MRI/TRUS FUSION guided biopsy as first approach in ambulatory setting: Feasibility and performance of a new fusion device

机译:MRI / TRUS FUSION引导活检是非卧床环境中的第一种方法:新型融合设备的可行性和性能

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Purpose: To evaluate the detection rate of Magnetic Resonance Imaging/Transrectal Ultrasound (MRI/TRUS) Fusion Biopsy performed in a series of patients with suspicious prostate cancer in an ambulatory setting.Materials and methods: Between March 2018 and January 2019 a series of 155 patients undergoing MRI/TRUS fusionguided biopsy were prospectively enrolled. All patients presented a suspected diagnosis for prostate cancer because of raised Prostate Specific Antigen (PSA) serum level and/or abnormal physical examination (digital rectal examination), and showed at least one suspicious area at the multiparametric Magnetic Resonance Imaging (mpMRI). Results: Of 155 patients, 58 (37.4%) were biopsy-na?ve, 97 (62.6%) had at least 1 previous negative TRUS-guided biopsy. The median age of the patient cohort was 66 years (IQR, 61- 69); the median prebiopsy PSA value was 7.1 ng/ml (IQR, 5- 8.9). Overall, the Fusion-TB findings were positive in 94 of 155 patients with a detection rate (DR) of 60%; a significantly high DR was obtained in terms of clinically significant prostate cancer (csPCa) by Fusion-TB (61 pts; 41.9%). The overall DR in the 121 biopsy-naive patients was 60.6%. In the subgroup of the 34 patients with at least 1 previous set of TRUS-GB, overall DR was 39.3% (35/50). Conclusions: The targeted MRI/TRUS fusion-guided biopsy represents a safe and accurate approach for diagnosis of csPCa, especially in patient with previous TRUS guided biopsy negative and suspicious prostate cancer.
机译:目的:评估在一系列可疑前列腺癌患者在非卧床环境中进行的磁共振成像/经直肠超声(MRI / TRUS)融合活检的检出率。材料和方法:2018年3月至2019年1月期间进行的一系列155次检查接受MRI / TRUS融合引导活检的患者。由于前列腺特异性抗原(PSA)血清水平升高和/或体格检查异常(直肠指检),所有患者均被诊断为前列腺癌,并在多参数磁共振成像(mpMRI)处显示至少一个可疑区域。结果:在155例患者中,有58例(37.4%)未进行活检,有97例(62.6%)曾接受过至少1次TRUS阴性的活检。患者队列的中位年龄为66岁(IQR,61-69);活检前PSA的中位数为7.1 ng / ml(IQR,5- 8.9)。总体而言,在155例患者中,有94例的融合结核阳性结果为阳性,检出率(DR)为60%。 Fusion-TB在临床上具有重要意义的前列腺癌(csPCa)方面获得了显着高的DR(61分; 41.9%)。 121例未进行活检的患者的总DR为60.6%。在34例患者中,至少有一组先前的TRUS-GB组的亚组中,总DR为39.3%(35/50)。结论:靶向MRI / TRUS融合引导活检代表了一种诊断csPCa的安全,准确的方法,尤其是对于先前接受TRUS引导活检阴性和可疑前列腺癌的患者。

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