Zhou Ming, Li Jianbo, Cheng Liang, Egevad Lars, Deng Fang-Ming, Kunju Lakshmi Priya, Magi-Galluzzi Cristina, Melamed Jonathan, Mehra Rohit, Mendrinos Savvas, Osunkoya Adeboye O, Paner Gladell, Shen Steve S, Tsuzuki Toyonori, Trpkov Kiril, Tian Wei, Yang Ximing, Shah Rajal B
*New York University Medical Center, New York, NY †Cleveland Clinic, Cleveland, OH ‡Indiana University, Indianapolis, IN ∥The University of Michigan, Ann Arbor, MI ¶Division of Urologic Pathology, Miraca Life Sciences Research Institute, Miraca Life Sciences, Irving ††Houston Methodist Hospital, Houston, TX #Emory University School of Medicine, Atlanta, GA **University of Chicago ∥∥Northwestern Medical Center, Chicago, IL §Karolinska Institutet, Stockholm, Sweden ‡‡Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan §§Calgary Laboratory Services and University of Calgary, Calgary, AB, Canada.
Am J Surg Pathol. 2015 Oct;39(10):1331-9. doi: 10.1097/PAS.0000000000000457.
Accurate recognition of Gleason pattern (GP) 4 prostate carcinoma (PCa) on needle biopsy is critical for patient management and prognostication. "Poorly formed glands" are the most common GP4 subpattern. We studied the diagnostic reproducibility and the quantitative threshold of grading GP4 "poorly formed glands" and the criteria to distinguish them from tangentially sectioned GP3 glands. Seventeen urologic pathologists were first queried for the definition of "poorly formed glands" using cases representing a spectrum of PCa glandular differentiation. Cancer glands with no or rare lumens, elongated compressed glands, and elongated nests were considered "poorly formed glands" by consensus. Participants then graded a second set of 23 PCa cases that potentially contained "poorly formed glands" with a fair interobserver agreement (κ = 0.34). The consensus diagnoses, defined as agreement by > 70% participants, were then correlated with the quantitative (≤ 5, 6 to 10, >10) and topographic features of poorly formed glands (clustered, immediately adjacent to, and intermixed with other well-formed PCa glands) in each case. Poorly formed glands immediately adjacent to other well-formed glands regardless of their number and small foci of ≤ 5 poorly formed glands regardless of their location were not graded as GP4. In contrast, large foci of >10 poorly formed glands that were not immediately adjacent to well-formed glands were graded as GP4. Grading "poorly formed glands" is challenging. Some morphologic features are, however, reproducible for and against a GP4 diagnosis. This study represents an important step in standardization of grading of "poorly formed glands" based on quantitative and topographic morphologic features.
在穿刺活检中准确识别 Gleason 4 级前列腺癌(PCa)对于患者管理和预后判断至关重要。“形态不佳的腺体”是最常见的 Gleason 4 级亚型。我们研究了 Gleason 4 级“形态不佳的腺体”分级的诊断可重复性、定量阈值以及将它们与斜切的 Gleason 3 级腺体区分开来的标准。首先,向 17 位泌尿外科病理学家询问“形态不佳的腺体”的定义,使用代表一系列 PCa 腺分化的病例。通过共识,无或罕见管腔的癌性腺体、细长压缩的腺体和细长的巢状结构被视为“形态不佳的腺体”。参与者随后对第二组 23 例可能包含“形态不佳的腺体”的 PCa 病例进行分级,观察者间一致性尚可(κ = 0.34)。然后将共识诊断(定义为超过 70%参与者达成一致)与每个病例中形态不佳的腺体的定量(≤5、6 至 10、>10)和地形特征(聚集、紧邻以及与其他形态良好的 PCa 腺体混合)相关联。无论数量多少,紧邻其他形态良好腺体的形态不佳的腺体以及无论位置如何、≤5 个形态不佳腺体的小灶均不分级为 Gleason 4 级。相反,不紧邻形态良好腺体的>10 个形态不佳腺体的大灶分级为 Gleason 4 级。对“形态不佳的腺体”进行分级具有挑战性。然而,一些形态学特征对于支持或反对 Gleason 4 级诊断是可重复的。这项研究是基于定量和地形形态学特征对“形态不佳的腺体”分级进行标准化的重要一步。