Hida Akira I, Omanovic Dzenita, Pedersen Lars, Oshiro Yumi, Ogura Takashi, Nomura Tsunehisa, Kurebayashi Junichi, Kanomata Naoki, Moriya Takuya
Department of Pathology, Matsuyama Shimin Hospital, Matsuyama, Japan.
Department of Pathology, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Histopathology. 2020 Sep;77(3):471-480. doi: 10.1111/his.14140. Epub 2020 Sep 11.
Precise evaluation of proliferative activity is essential for the stratified treatment of luminal-type breast cancer (BC). Immunohistochemical staining of Ki-67 has been widely used to determine proliferative activity and is recognised to be a useful prognostic marker. However, there remains discussion concerning the methodology. We aimed to develop an automated and reliable Ki-67 assessment approach for invasive BC.
A retrospective study was designed to include two cohorts consisting of 152 and 261 consecutive patients with luminal-type BC. Representative tissue blocks following surgery were collected, and three serial sections were stained automatically with Ki-67, pan-cytokeratin and p63. The whole slides were scanned digitally and aligned using VirtualTripleStaining - an extension to the VirtualDoubleStaining™ technique provided by Visiopharm software. The aligned files underwent automated invasive cancer detection, hot-spot identification and Ki-67 counting. The automated scores showed a significant positive correlation with the pathologists' scores (r = 0.82, P < 0.0001). Among selected patients with curative surgery and standard adjuvant therapies (n = 130), the digitally assessed low Ki-67 group (<20%) demonstrated a significantly better prognosis (breast cancer-specific survival, P = 0.030; hazard ratio = 0.038) than the high Ki-67 group.
Digital image analysis yielded similar results to the scores determined by experienced pathologists. The prognostic utility was verified in our cohort, and an automated process is expected to have high reproducibility. Although some pitfalls were confirmed and thus need to be monitored by laboratory staff, the application could be utilised for the assessment of BC.
精确评估增殖活性对于管腔型乳腺癌(BC)的分层治疗至关重要。Ki-67免疫组化染色已广泛用于确定增殖活性,并且被认为是一种有用的预后标志物。然而,关于该方法仍存在争议。我们旨在开发一种用于浸润性BC的自动化且可靠的Ki-67评估方法。
设计了一项回顾性研究,纳入两个队列,分别由152例和261例连续的管腔型BC患者组成。收集术后代表性组织块,并用Ki-67、全细胞角蛋白和p63对三个连续切片进行自动染色。对整个玻片进行数字扫描,并使用VirtualTripleStaining进行对齐,这是Visiopharm软件提供的VirtualDoubleStaining™技术的扩展。对齐后的文件进行自动浸润癌检测、热点识别和Ki-67计数。自动评分与病理学家的评分呈显著正相关(r = 0.82,P < 0.0001)。在接受根治性手术和标准辅助治疗的选定患者(n = 130)中,数字评估的低Ki-67组(<20%)的预后(乳腺癌特异性生存,P = 0.030;风险比 = 0.038)明显优于高Ki-67组。
数字图像分析得出的结果与经验丰富的病理学家确定的评分相似。在我们的队列中验证了其预后效用,并且预计自动化过程具有高重复性。尽管确认了一些缺陷,因此需要实验室工作人员进行监测,但该应用可用于BC的评估。