Prospective study of prostate cancer detection using multiparametric magnetic resonance imaging ultrasound-guided fusion, standard, and saturation biopsy

V. Petov, E. Y. Timofeeva, A. Bazarkin, A. Morozov, M. Taratkin, T. Ganzha, S. Danilov, Y. Chernov, A. Abdusalamov, A. Amosov, D. V. Enikeev, G. Krupinov
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Abstract

Background. Currently, about 80 % of men with low-grade prostate cancer (per ISUP 1 (International Society of Urological Pathology)) have indications for radical treatment. Overdiagnosis of low-grade cancer is associated with the use of systematic biopsy methods (standard transrectal, saturation) under ultrasound control for diagnosis verification. To improve prostate cancer diagnosis, the European Association of Urology (2019) recommended multiparametric magnetic resonance imaging before biopsy, and in case of detection of a suspicious lesion magnetic resonance imaging (MRI)-targeted biopsy. In clinical practice, the most common method of MRI-targeted biopsy is multiparametric MRI ultrasound-guided (mpMRI/US) fusion biopsy. However, some studies show contradictory results in detection of prostate cancer using systematic and MRI-targeted biopsy techniques.Aim. To compare detection of clinically significant prostate cancer (ISUP ≥2) using mpMRI/US fusion, standard, and saturation biopsy.Materials and methods. The study included 96 patients. The following inclusion criteria were applied: prostate-specific antigen >2 ng/mL and/or detection of a suspicious lesion during digital rectal and/or transrectal ultrasound examination, and PI-RADS (Prostate Imaging Reporting and Data System) v.2.1 score ≥3. At the first stage, “unblinded” urologist performed a transperineal mpMRI/US fusion and saturation biopsies. At the second stage, “blinded” urologist performed standard transrectal biopsy. Clinically significant cancer was defined as ISUP ≥2.Results. Median age was 63 years, prostate volume – 47 cm3, prostate-specific antigen – 6.82 ng/mL. MpMRI/US fusion, standard, and saturation biopsies were comparable in regard to the rate of detection of clinically significant (29, 24, 28 %; p = 0.81) and clinically insignificant (25, 26, 35 %; p = 0.43) cancer. Overall prostate cancer detection rates were also similar: 54, 50, 63 %, respectively (p = 0.59). The percentages of positive cores in mpMRI/US fusion, standard, and saturation biopsies were 33, 10 and 13 %, respectively (p <0.01). The maximal core length in mpMRI/US was 6.4 mm, in standard biopsy – 6.35 mm, in saturation biopsy – 5.1 mm (p = 0.7).Conclusion. Detection rates of clinically significant, clinically insignificant prostate cancer and overall detection rate are comparable between systematic biopsy techniques and mpMRI/US fusion biopsy.
超声引导下多参数磁共振成像融合、标准和饱和活检检测前列腺癌的前瞻性研究
背景。目前,大约80%的低级别前列腺癌男性患者(根据国际泌尿病理学学会)有根治性治疗的适应症。低级别癌症的过度诊断与在超声控制下使用系统活检方法(标准经直肠,饱和)进行诊断验证有关。为了提高前列腺癌的诊断,欧洲泌尿外科协会(2019)建议在活检前进行多参数磁共振成像,并在检测到可疑病变时进行磁共振成像(MRI)靶向活检。在临床实践中,最常见的MRI靶向活检方法是多参数MRI超声引导(mpMRI/US)融合活检。然而,一些研究表明,在使用系统活检技术和mri靶向活检技术检测前列腺癌方面,结果相互矛盾。比较mpMRI/US融合、标准和饱和活检对临床显著前列腺癌(ISUP≥2)的检测。材料和方法。该研究包括96名患者。纳入标准:前列腺特异性抗原>2 ng/mL和/或直肠指检和/或经直肠超声检查发现可疑病变,PI-RADS(前列腺影像报告和数据系统)v.2.1评分≥3。在第一阶段,“无盲”泌尿科医生进行了经会阴mpMRI/US融合和饱和度活检。在第二阶段,“盲法”泌尿科医生进行了标准的经直肠活检。临床上有显著意义的肿瘤定义为ISUP≥2。中位年龄63岁,前列腺体积- 47 cm3,前列腺特异性抗原- 6.82 ng/mL。MpMRI/US融合、标准活检和饱和活检在临床意义上的检出率相当(29,24,28%;P = 0.81),临床差异不显著(25,26,35 %;P = 0.43)。总体前列腺癌检出率也相似:分别为54%、50%、63% (p = 0.59)。mpMRI/US融合活检、标准活检和饱和活检中核阳性率分别为33.10%和13% (p <0.01)。mpMRI/US最大核长度为6.4 mm,标准活检为6.35 mm,饱和活检为5.1 mm (p = 0.7)。系统活检技术与mpMRI/US融合活检技术对临床显著性和临床不显著性前列腺癌的检出率和总体检出率相当。
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