Chatterjee Aritrick, Gallan Alexander, Fan Xiaobing, Medved Milica, Akurati Pranadeep, Bourne Roger M, Antic Tatjana, Karczmar Gregory S, Oto Aytekin
Department of Radiology, University of Chicago, Chicago, IL 60637, USA.
Sanford J. Grossman Center of Excellence in Prostate Imaging and Image Guided Therapy, University of Chicago, Chicago, IL 60637, USA.
Cancers (Basel). 2023 Dec 13;15(24):5825. doi: 10.3390/cancers15245825.
We investigated why some prostate cancers (PCas) are not identified on multiparametric MRI (mpMRI) by using ground truth reference from whole-mount prostatectomy specimens. A total of 61 patients with biopsy-confirmed PCa underwent 3T mpMRI followed by prostatectomy. Lesions visible on MRI prospectively or retrospectively identified after correlating with histology were considered "identified cancers" (ICs). Lesions that could not be identified on mpMRI were considered "unidentified cancers" (UCs). Pathologists marked the Gleason score, stage, size, and density of the cancer glands and performed quantitative histology to calculate the tissue composition. Out of 115 cancers, 19 were unidentified on MRI. The UCs were significantly smaller and had lower Gleason scores and clinical stage lesions compared with the ICs. The UCs had significantly ( < 0.05) higher ADC (1.34 ± 0.38 vs. 1.02 ± 0.30 μm/ms) and T2 (117.0 ± 31.1 vs. 97.1 ± 25.1 ms) compared with the ICs. The density of the cancer glands was significantly ( = 0.04) lower in the UCs. The percentage of the Gleason 4 component in Gleason 3 + 4 lesions was nominally ( = 0.15) higher in the ICs (20 ± 12%) compared with the UCs (15 ± 8%). The UCs had a significantly lower epithelium (32.9 ± 21.5 vs. 47.6 ± 13.1%, = 0.034) and higher lumen volume (20.4 ± 10.0 vs. 13.3 ± 4.1%, = 0.021) compared with the ICs. Independent from size and Gleason score, the tissue composition differences, specifically, the higher lumen and lower epithelium in UCs, can explain why some of the prostate cancers cannot be identified on mpMRI.
我们通过使用全层前列腺切除标本的真实参考,研究了为什么某些前列腺癌(PCa)在多参数磁共振成像(mpMRI)上未被识别。共有61例经活检确诊为PCa的患者接受了3T mpMRI检查,随后进行了前列腺切除术。在与组织学相关后,前瞻性或回顾性在MRI上可见的病变被视为“已识别癌症”(ICs)。在mpMRI上无法识别的病变被视为“未识别癌症”(UCs)。病理学家标记了癌腺的Gleason评分、分期、大小和密度,并进行定量组织学分析以计算组织组成。在115例癌症中,19例在MRI上未被识别。与ICs相比,UCs明显更小,Gleason评分和临床分期病变更低。与ICs相比,UCs的表观扩散系数(ADC)明显更高(1.34±0.38对1.02±0.30μm/ms),T2值更高(117.0±31.1对97.1±25.1ms)(P<0.05)。UCs中癌腺的密度明显更低(P = 0.04)。在Gleason 3+4病变中,Gleason 4成分的百分比在ICs中(20±12%)比UCs中(15±8%)名义上更高(P = 0.15)。与ICs相比,UCs的上皮细胞明显更少(32.9±21.5对47.6±13.1%,P = 0.034),管腔体积更大(20.4±10.0对13.3±4.1%,P = 0.021)。独立于大小和Gleason评分,组织组成差异,特别是UCs中更高的管腔和更低的上皮细胞,可以解释为什么某些前列腺癌在mpMRI上无法被识别。