Haas M, Günzel K, Penzkofer T, Maxeiner A, Fischer T, Miller K, Hamm B, Asbach P, Cash H
Department of Radiology, Charité, Berlin.
Department of Urology, Charité, Berlin.
Aktuelle Urol. 2016 Sep;47(5):383-7. doi: 10.1055/s-0042-111128. Epub 2016 Sep 28.
A revised version of the PI-RADS scoring system has been introduced and score-related variability between version 1 and 2 may be suspected. This study aimed to assess the PI-RADS scores derived from version 1 (v1) and the updated version 2 (v2).
61 patients with biopsy-proven prostate cancer (PCa) and 90 lesions detected on pre-biopsy 3-Tesla multiparametric MRI were included in this retrospective analysis. 2 experienced radiologists scored all lesions in consensus. Lesion scores differing between PI-RADS v1 and v2 were further analyzed. Histology data from radical prostatectomy (RP) were included when available.
The PI-RADS v1 and v2 score differed in 52% of patients (32/61) and in 39% of lesions (35/90). On a lesion basis, the reason for the differences were related to sum score in v1 vs. categorical system in v2 in 51% (18/35) of lesions, cutoff between PI-RADS 4 and 5 based on lesion size in v2 as opposed to the sum score in v1 in 31% (11/35) and were inconclusive in 17% (6/35). The RP subgroup indicates enhanced detection of PCas with GS 3+3 and GS 3+4 in v2.
PI-RADS scores of prostatic lesions frequently differed between v1 and v2, the major reasons for these differences being score-related. In men undergoing RP, PI-RADS v2 improved detection of low risk PCa, but did not increase accuracy for discrimination of GS 3+4 vs. GS≥4+3 compared to v1. Urologists should be aware of the system-related differences when interpreting PI-RADS scores.
PI-RADS评分系统的修订版已推出,可能会怀疑第1版和第2版之间与评分相关的变异性。本研究旨在评估源自第1版(v1)和更新的第2版(v2)的PI-RADS评分。
本回顾性分析纳入了61例经活检证实为前列腺癌(PCa)的患者以及在活检前3特斯拉多参数MRI上检测到的90个病变。2名经验丰富的放射科医生对所有病变进行了一致评分。进一步分析了PI-RADS v1和v2之间不同的病变评分。如有可用,纳入了根治性前列腺切除术(RP)的组织学数据。
52%(32/61)的患者和39%(35/90)的病变中PI-RADS v1和v2评分不同。在病变层面,差异的原因在51%(18/35)的病变中与v1中的总分系统与v2中的分类系统有关,在31%(11/35)的病变中与v2中基于病变大小的PI-RADS 4和5之间的临界值有关,而不是v1中的总分,在17%(6/35)的病变中尚无定论。RP亚组表明v2中对GS 3+3和GS 3+4的PCa检测有所增强。
前列腺病变的PI-RADS评分在v1和v2之间经常不同,这些差异的主要原因与评分相关。在接受RP的男性中,PI-RADS v2改善了低风险PCa的检测,但与v1相比,并未提高区分GS 3+4与GS≥4+3的准确性。泌尿外科医生在解读PI-RADS评分时应意识到系统相关的差异。