Academic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Pathology, Faculty of Medicine, Menoufia University, Shebin El Kom, Egypt.
Histopathology. 2022 Dec;81(6):786-798. doi: 10.1111/his.14781. Epub 2022 Sep 19.
Ki67 reflects the proliferation activity in breast cancer (BC). However, an optimal method for its assessment in clinical settings has yet to be robustly defined. In this study we compared several methods to score Ki67 to identify a reliable and reproducible method for routine practice.
Sections from luminal BC cohort (n = 1662) were immunohistochemically stained with Ki67 and were assessed for the percentage, pattern, and intensity of expression. Ki67 positivity was evaluated using three methods: (i) quantification of Ki67-positive cells among 1000 invasive tumour cells within hotspot, (ii) average estimation of Ki67 within a defined hotspot, and (iii) average estimation of Ki67 positivity within the whole section. Time required for scoring, interobserver agreement and association with outcome were determined.
The mean percentage of Ki67 expression per 1000 cells method was 16%, while the mean value of Ki67 scores using the average estimation within hotspot and whole slide were 14% and 12%, respectively. Quantification of Ki67-positive cells within 1000 cells had the highest degree of consistency between observers, and the highest hazard ratio predicting patient outcome when compared to using different common Ki67 cutoffs, which was independent of the other two methods. Granular pattern of Ki67 expression was associated with poorer outcome as compared to the other patterns.
Assessment of Ki67 expression using quantification positive cells among 1000 tumour cells is an optimal method to achieve high reliability and reproducibility. Comment on the predominant Ki67 expression pattern would add prognostic and predictive value in luminal BC.
Ki67 反映了乳腺癌(BC)的增殖活性。然而,其在临床环境中的评估方法尚未得到充分定义。在这项研究中,我们比较了几种评分 Ki67 的方法,以确定一种可靠且可重复的常规实践方法。
对腔型 BC 队列(n=1662)的切片进行 Ki67 免疫组织化学染色,并评估其表达的百分比、模式和强度。Ki67 阳性采用三种方法进行评估:(i)在热点中对 1000 个浸润性肿瘤细胞中的 Ki67 阳性细胞进行定量,(ii)在定义的热点内对 Ki67 进行平均估计,(iii)在整个切片内对 Ki67 阳性进行平均估计。确定评分所需的时间、观察者间的一致性以及与结果的相关性。
每 1000 个细胞的 Ki67 表达平均百分比方法为 16%,而使用平均热点和整个切片内 Ki67 评分的平均值分别为 14%和 12%。在 1000 个细胞内定量 Ki67 阳性细胞在观察者之间具有最高的一致性,并且与使用不同常见 Ki67 截止值相比,预测患者预后的风险比最高,这是独立于其他两种方法的。与其他模式相比,Ki67 表达的颗粒状模式与较差的预后相关。
使用 1000 个肿瘤细胞中的定量阳性细胞评估 Ki67 表达是实现高可靠性和可重复性的最佳方法。对 Ki67 表达模式的主要评论将在腔型 BC 中增加预后和预测价值。