大筛状癌和“不良组织学”与其他Gleason模式4亚型的相关性:一项原则性研究评估了485例根治性前列腺切除术标本,并提出了“边缘组织学”的概念。

IF 1.5 4区 医学 Q3 PATHOLOGY
Jane K Nguyen, Jianbo Li, Chien-Kuang C Ding, Christopher J Weight, Jesse K McKenney
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引用次数: 0

摘要

前列腺腺癌合并大筛状腺/导管内癌(LC/IDC),或最近提出的不良组织学,与根治性前列腺切除术后的不良预后相关。然而,没有LC/IDC(或不良组织学)的Gleason 4型癌在前列腺切除术后出现侵袭性临床行为的风险最小。作为原则性研究,我们收集了485例根治性前列腺切除术标本,以评估不同亚型Gleason 4型疾病与邻近高危前列腺腺癌(定义为LC/IDC或不良组织学)存在之间的相关性。所有的前列腺切除术都完全包埋,所有的切片都重新检查以记录Gleason评分/分级组,最大筛状腺的直径(即最长的横截距离),以及使用先前描述的Canary方法的所有癌的结构模式。测定LC/IDC(定义为>0.25 mm)的存在和百分比。我们还评估了与最近提出的“不良组织学”作为次要终点的相关性。复杂Gleason模式4亚型,不同于LC/IDC和不利的组织学,被称为“交界性组织学”,定义为存在以下任何一种模式:小筛状/肾小球结构(≤0.25 mm),优势群体形成不良的腺体/小巢,简单的肾小球,以及与黏液外渗相关的上皮复杂性(超出典型的黏液纤维增生模式,不含筛状>0.25 mm)。记录变量与LC/IDC(或不利组织学)之间的比较使用连续变量的Wilcoxon检验和分类变量的卡方检验或Fisher检验。使用Pearson或phi相关系数来评估两个变量之间的关联。“边缘组织学”与LC/IDC (r = 0.55)和不良组织学(r = 0.607)显著相关,均为p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation of large cribriform carcinoma and "unfavorable histology" with other Gleason pattern 4 subtypes: A proof-of-principle study evaluating 485 radical prostatectomy specimens with proposal for the concept of "borderline histology".

Prostatic adenocarcinomas with large cribriform glands/intraductal carcinoma (LC/IDC), or the recently proposed unfavorable histology, are associated with adverse outcomes after radical prostatectomy. However, Gleason pattern 4 carcinomas without LC/IDC (or unfavorable histology) have minimal risk for aggressive clinical behavior after prostatectomy. As proof-of-principle study, we collected a cohort of 485 radical prostatectomy specimens to assess correlations between different subtypes of Gleason pattern 4 disease and the presence of adjacent high-risk prostatic adenocarcinoma, defined as LC/IDC or unfavorable histology. All prostatectomies were completely embedded, and all slides re-reviewed to record Gleason score/Grade Group, diameter of the largest cribriform gland (i.e. the longest cross-sectional distance), and all architectural patterns of carcinoma utilizing previously described Canary methodology. The presence and percent of LC/IDC (defined as >0.25 mm) was determined. We also evaluated correlation with the recently proposed "unfavorable histology" as a secondary endpoint. Complex Gleason pattern 4 subtypes, distinct from LC/IDC and unfavorable histology, were termed "borderline histology" and defined as the presence of any of the following patterns: small cribriform/glomeruloid architecture (≤0.25 mm), dominant population of poorly formed glands/small nests, simple glomerulations, and epithelial complexity associated with extravasated mucin (beyond typical mucinous fibroplasia pattern and not containing cribriform >0.25 mm). Comparisons between recorded variables and LC/IDC (or unfavorable histology) utilized the Wilcoxon test for continuous variables and chi-squared test or Fisher's test for categorical variables. Pearson or phi correlation coefficients were used to assess the association between two variables. "Borderline histology" was significantly correlated to LC/IDC (r = 0.55) and unfavorable histology (r = 0.607), both p < 0.001. Specifically, small cribriform/small glomeruloid architecture had the strongest correlation, compared to the other "borderline histology" subtypes (r = 0.646). We demonstrate that "borderline histology" has a strong association with the concomitant presence of high-risk prostate cancer by current histologic definitions (i.e. LC/IDC and unfavorable histology). This proof-of-principle study suggests that large cohort biopsy-RP correlation studies are needed, as the presence of these patterns on biopsy could potentially aid preoperative risk stratification for patients without other high-risk features at initial evaluation.

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来源期刊
CiteScore
3.90
自引率
5.00%
发文量
149
审稿时长
26 days
期刊介绍: A peer-reviewed journal devoted to the publication of articles dealing with traditional morphologic studies using standard diagnostic techniques and stressing clinicopathological correlations and scientific observation of relevance to the daily practice of pathology. Special features include pathologic-radiologic correlations and pathologic-cytologic correlations.
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