3-Tesla 多参数磁共振成像的前列腺癌多灶性和可检测性:与根治性前列腺切除术映射组织病理学的相关性

IF 2.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Serdar Karadağ, Deniz Noyan Özlü, Ahmet Hacıislamoğlu, Ömer Yıldız, Halil Fırat Baytekin, Mithat Ekşi, Hakan Polat, Alper Bitkin, Ali İhsan Taşçı
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引用次数: 0

摘要

背景。我们旨在利用 3-Tesla (3T) 多参数磁共振成像(mpMRI)确定前列腺癌(Pca)的多发性和可检测性。方法对 2020 年 4 月至 2021 年 4 月期间在我院接受根治性前列腺切除术的患者数据进行分析。患者在前列腺癌根治术阶段被纳入研究。回顾性收集人口统计学和组织病理学数据,然后重新评估符合研究条件的患者的磁共振成像。可疑感兴趣区(ROI)由一名在泌尿放射学领域有四年经验的放射科医生进行评估,并根据前列腺成像报告和数据系统(PIRADS)v2.1进行评分。阅读者对任何活检标本的病理结果都是盲人。PIRADS评分≥3分的病变被视为阳性并纳入研究。所有病例均由一位在泌尿病理学领域有十年经验的病理学家进行组织病理学评估。我们采用了制图法,该方法在处理整个前列腺切除标本的同时,还能提供与全切组织病理学完全相同的信息。结果70 名患者中共发现 142 处组织病理学肿瘤病变。术后组织病理学结果显示,78.6%(55 人)的肿瘤为多发性,142 个病灶中有 52.1%(74 人)具有临床意义。通过检测总共 67 个病灶,mpMRI 显示出 47% 的总体灵敏度。对有临床意义病灶的灵敏度为 73%(54/74),而对无临床意义病灶的灵敏度仅为 17.6%(12/68)。在检测出肿瘤的组别中,平均前列腺特异性抗原(PSA)和PSA密度更高,高级别病变更多,前列腺外扩展率明显更高(P分别为0.05)。根据多变量分析,只有肿瘤大小和格里森评分(GS)是 mpMRI 检测前列腺内肿瘤病灶能力的独立预测因素(p < 0.0001)。mpMRI在检测高危和大的前列腺肿瘤灶方面表现出了可接受的灵敏度。据观察,对于小肿瘤、低GS肿瘤和非指数肿瘤,诊断准确性明显降低。相当比例的漏诊病灶具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multifocality and Detectability of Prostate Cancer with 3-Tesla Multiparametric Magnetic Resonance Imaging: Correlation with Radical Prostatectomy Mapping Histopathology

Multifocality and Detectability of Prostate Cancer with 3-Tesla Multiparametric Magnetic Resonance Imaging: Correlation with Radical Prostatectomy Mapping Histopathology

Background. We aimed to determine the multifocality and detectability of prostate cancer (Pca) with 3-Tesla (3T) multiparametric magnetic resonance imaging (mpMRI). Methods. The data of the patients who underwent radical prostatectomy in our institution between April 2020 and April 2021 were analyzed. Patients were included in the study at the stage of radical prostatectomy. Demographic and histopathological data were retrospectively collected, and then MRIs of eligible patients were re-evaluated for the study. Suspicious regions of interest (ROIs) were evaluated by a radiologist with 4 years of experience in uroradiology and scored based on Prostate Imaging Reporting and Data System (PIRADS) v2.1. The reader was blinded to the pathological outcomes of any biopsy specimen. Lesions with a PIRADS score ≥3 were considered positive and included in the study. All cases were evaluated histopathologically by a pathologist with ten years of experience in uropathology. We utilized the mapping method which provided exactly the same information as the whole-mount histopathology along with processing the entire prostatectomy specimen. Results. A total of 142 histopathologic tumoral lesions were detected among 70 patients. In relation to postoperative histopathology, tumor multifocality was established in 78.6% (n = 55), and 52.1% (n = 74) of 142 foci recognized were clinically significant. By detecting a total of 67 lesions, mpMRI showed an overall sensitivity of 47%. Whilst the sensitivity was 73% (54/74) in clinically significant lesions, the sensitivity was only 17.6% (12/68) in clinically insignificant lesions. For the group with detected tumors, the mean prostate-specific antigen (PSA) and PSA density were higher, there were more high-grade lesions, and the rate of the extraprostatic extension was significantly greater (p < 0.05, respectively). According to the multivariate analysis, only tumor size and Gleason Score (GS) were independent predictors regarding the ability of mpMRI to detect tumor foci within the prostate (p < 0.0001). Conclusion. mpMRI exhibited an acceptable sensitivity in detecting high-risk and large Pca foci. The diagnostic accuracy is observed to be markedly diminished in small, low GS, and nonindex tumors. A considerable percentage of missed lesions are clinically significant.

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来源期刊
CiteScore
5.30
自引率
0.00%
发文量
274
审稿时长
3-8 weeks
期刊介绍: IJCP is a general medical journal. IJCP gives special priority to work that has international appeal. IJCP publishes: Editorials. IJCP Editorials are commissioned. [Peer reviewed at the editor''s discretion] Perspectives. Most IJCP Perspectives are commissioned. Example. [Peer reviewed at the editor''s discretion] Study design and interpretation. Example. [Always peer reviewed] Original data from clinical investigations. In particular: Primary research papers from RCTs, observational studies, epidemiological studies; pre-specified sub-analyses; pooled analyses. [Always peer reviewed] Meta-analyses. [Always peer reviewed] Systematic reviews. From October 2009, special priority will be given to systematic reviews. [Always peer reviewed] Non-systematic/narrative reviews. From October 2009, reviews that are not systematic will be considered only if they include a discrete Methods section that must explicitly describe the authors'' approach. Special priority will, however, be given to systematic reviews. [Always peer reviewed] ''How to…'' papers. Example. [Always peer reviewed] Consensus statements. [Always peer reviewed] Short reports. [Always peer reviewed] Letters. [Peer reviewed at the editor''s discretion] International scope IJCP publishes work from investigators globally. Around 30% of IJCP articles list an author from the UK. Around 30% of IJCP articles list an author from the USA or Canada. Around 45% of IJCP articles list an author from a European country that is not the UK. Around 15% of articles published in IJCP list an author from a country in the Asia-Pacific region.
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