临床怀疑患有前列腺癌症但无可疑双参数磁共振成像结果且前列腺特异性抗原密度<0.15 ng/mL的生物合成男性避免活检的早期经验2:一项为期2年的随访研究

IF 0.9 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Acta radiologica open Pub Date : 2022-04-01 DOI:10.1177/20584601221094825
Karen-Cecilie Kortenbach, V. Løgager, H. Thomsen, L. Boesen
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引用次数: 3

摘要

背景关于结合双参数(bp)磁共振成像(MRI)和前列腺特异性抗原密度(PSAd)排除活检的诊断准确性,只有有限的数据发表。目的本研究旨在评估在无可疑bp MRI和PSAd<0.15 ng/mL2的男性中,遵循避免立即活检的策略,诊断为sPCa的2年风险。材料和方法2019年3月至7月,200名临床怀疑前列腺癌的活检幼稚男性接受了活检前bp MRI检查。其中,109名男性的前列腺成像报告和数据系统(PI-RADS)评分为1-3,其中77名男性的PSAd计算值<0.15 ng/mL2。因此,在这77名男性中没有进行活检,他们进行了至少2年的临床随访,并在怀疑sPCa增加的情况下重新检查。其余32名计算PSAd≥0.15 ng/mL2的男性接受了系统活检和任何PI-RADS 3病变的靶向活检。结果77名男性中有1名(1.3%)在随访2年内被诊断为sPCa。所有男性在1年内被转诊回其全科医生,9%(7/77)在随访期间被转诊到泌尿外科。在这些男性中,43%(3/7)的PSA水平在确认测试中仍高于个人阈值,并接受了二次MRI扫描。结论对于bpMRI结果显示最大PI-RADS 3且PSAd<0.15 ng/mL2的男性,没有活检导致诊断为sPCa的2年风险为1.3%。
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Early experience in avoiding biopsies for biopsy-naïve men with clinical suspicion of prostate cancer but non-suspicious biparametric magnetic resonance imaging results and prostate-specific antigen density < 0.15 ng/mL2: A 2-year follow-up study
Background Only limited data have been published on the diagnostic accuracy of combining biparametric (bp) magnetic resonance imaging (MRI) and prostate-specific antigen density (PSAd) to rule out biopsies. Purpose The purpose is to assess the 2-year risk of being diagnosed with sPCa following the strategy of avoiding immediate biopsies in men with non-suspicious bp MRIs and a PSAd <0.15 ng/mL2. Material and Methods Two hundred biopsy-naïve men with clinical suspicion of PCa underwent a pre-biopsy bp MRI from March to July 2019. Of these, 109 men had a Prostate Imaging Reporting and Data System (PI-RADS) score of 1–3 including 77 men with calculated PSAd <0.15 ng/mL2. As a result, no biopsies were performed in these 77 men, who were clinically followed up for at least 2 years and re-examined in case of rising suspicion of sPCa. The remaining 32 men with a calculated PSAd ≥0.15 ng/mL2 underwent systematic biopsies and targeted biopsies of any PI-RADS 3 lesion. Results One of the 77 men (1.3%) had an sPCa diagnosed within 2 years of follow-up. All men were referred back to their general practitioner within 1 year and 9% (7/77) were re-referred to the urology department during follow-up. Among these men, 43% (3/7) continued to have PSA levels that were above their individual thresholds at confirmatory testing and underwent secondary MRI scans. Conclusions No biopsies for men with bpMRI results exhibiting maximum PI-RADS 3 and with a PSAd <0.15 ng/mL2 resulted in a 2-year risk of being diagnosed with sPCa of 1.3%.
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