Boyaci Ceren, Sun Wenwen, Hartman Johan, Ács Balázs
Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital, Stockholm, Sweden.
Breast Cancer Res. 2025 Sep 2;27(1):159. doi: 10.1186/s13058-025-02114-6.
Ki67 is a broadly available biomarker of proliferation with various approaches to its evaluation in breast cancer. The International Ki67 in Breast Cancer Working Group (IKWG) recommends calculating Ki67 globally across the tumor area, as this method offers high interobserver concordance. These recommendations have been integrated into many international breast cancer guidelines (ASCO, ESMO), yet there is no real-world data on if it improved inter-pathologists and inter-laboratory variability. Here, we present the first real-world data on the variability and impact of Ki67 scores on clinical decision-making in breast cancer when using hotspot scoring and after implementing IKWG global scoring method in clinical practice. We extracted hotspot and global scoring results from 4313 breast cancer patients from routine diagnostics, categorizing the scores into three clinical risk groups over a one-year period across two large breast centers in Stockholm, Sweden. Variability between pathologists was not clinically significant. The global scoring method improved inter-laboratory consistency but also led to a notable increase in cases classified as intermediate at both centers This has been captured in the 2022 Swedish clinical breast cancer guidelines recommending molecular profiling test for patients with Grade II, global Ki67 intermediate score, T1c / T2 breast cancer. To conclude, our findings demonstrate acceptable consistency in Ki67 scores among individual pathologists across both scoring methods, however high inter-laboratory variability was observed with hot spot scoring. Global Ki67 scoring demonstrated low inter-laboratory variability in real world breast cancer care, thereby increasing the reliability of Ki67 assessment in clinical decision-making.
Ki67是一种广泛应用的增殖生物标志物,在乳腺癌中有多种评估方法。国际乳腺癌Ki67工作组(IKWG)建议在整个肿瘤区域整体计算Ki67,因为这种方法具有较高的观察者间一致性。这些建议已被纳入许多国际乳腺癌指南(美国临床肿瘤学会、欧洲肿瘤内科学会),但尚无关于其是否改善了病理学家之间和实验室间差异的真实世界数据。在此,我们展示了关于在临床实践中使用热点评分以及实施IKWG整体评分方法后,Ki67评分的变异性及其对乳腺癌临床决策影响的首批真实世界数据。我们从常规诊断的4313例乳腺癌患者中提取了热点评分和整体评分结果,在瑞典斯德哥尔摩的两个大型乳腺中心,将这些评分在一年时间内分为三个临床风险组。病理学家之间的差异在临床上并不显著。整体评分方法提高了实验室间的一致性,但也导致两个中心被归类为中等风险的病例显著增加。这一情况已被纳入2022年瑞典临床乳腺癌指南,该指南建议对二级、整体Ki67评分为中等、T1c/T2期乳腺癌患者进行分子谱检测。总之,我们的研究结果表明,两种评分方法在个体病理学家之间的Ki67评分具有可接受的一致性,然而热点评分观察到较高的实验室间变异性。在真实世界的乳腺癌护理中,整体Ki67评分显示出较低的实验室间变异性,从而提高了Ki67评估在临床决策中的可靠性。