UK National External Quality Assessment Scheme for Immunocytochemistry and In-Situ Hybridisation.
Ralph Lauren Centre for Breast Cancer Research, Royal Marsden Hospital, London, UK.
Appl Immunohistochem Mol Morphol. 2021 Feb 1;29(2):86-94. doi: 10.1097/PAI.0000000000000899.
We examined data from 374 laboratories staining for Ki-67 as part of external quality assessment over 8 runs between 2013 and 2017 (total data sets=2601). One of 5 primary antibodies was used for 94.8% of submissions, with MIB-1 (Agilent Dako) comprising 58.8% of the total. Examining assessment score as a continuous variable showed the 30-9 (Ventana) and K2 (Leica Biosystems) clones were associated with the highest mean scores (17.0; 95% confidence interval, 16.8-17.2 and 16.3; 95% confidence interval, 15.9-16.6, respectively). Stain quality was not significantly different between them. Both were associated with significantly better staining compared with MIB-1 (Agilent Dako), MM1 (Leica Biosystems), and SP6 from various suppliers (P<0.05). Similarly, categorical assessment of "Good" versus "Not good" staining quality showed that the 30-9 and K2 clones were both significantly associated with "Good" staining (both P<0.001). Other methodological parameters were examined for significant primary antibody-specific effects; none were seen for 30-9, K2, or SP6. The MM1 clone was more likely to be associated with good quality staining when it was used with Leica Biosystems sourced antigen retrieval, detection, and platform, all statistically significant at P<0.01. MIB-1 was more likely to be associated with good quality staining results when it was used with Agilent Dako antigen retrieval, detection, and staining platforms (P<0.0001), and less likely at the same significance level when used with Leica Biosystems reagents and equipment. The data presented here show the importance of not just primary antibody choice but also matching that choice to other methodological factors.
我们检查了 2013 年至 2017 年 8 次外部质量评估中 374 个实验室检测 Ki-67 的数据(总数据集为 2601 个)。其中 5 种主要抗体中的 1 种用于 94.8%的提交,其中 MIB-1(Agilent Dako)占总数的 58.8%。将评估得分作为连续变量进行检查,发现 30-9(Ventana)和 K2(Leica Biosystems)克隆与最高平均得分相关(分别为 17.0;95%置信区间,16.8-17.2 和 16.3;95%置信区间,15.9-16.6)。它们的染色质量没有显著差异。与 MIB-1(Agilent Dako)、MM1(Leica Biosystems)和来自不同供应商的 SP6 相比,两者的染色质量都显著更好(均 P<0.05)。同样,“良好”与“不佳”染色质量的分类评估表明,30-9 和 K2 克隆都与“良好”染色显著相关(均 P<0.001)。还检查了其他方法学参数以确定是否存在主要抗体特异性影响;在 30-9、K2 或 SP6 中均未发现。当 MM1 克隆与 Leica Biosystems 来源的抗原修复、检测和平台一起使用时,它更有可能与良好的染色质量相关,所有这些都具有统计学意义(均 P<0.01)。当 MIB-1 与 Agilent Dako 抗原修复、检测和染色平台一起使用时,它更有可能与良好的染色质量结果相关(P<0.0001),而当与 Leica Biosystems 试剂和设备一起使用时,其相关性则不那么显著。这里呈现的数据表明,不仅选择主要抗体很重要,而且将该选择与其他方法学因素匹配也很重要。