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病理学中Ki67评估的质量保证试验

Quality assurance trials for Ki67 assessment in pathology.

作者信息

Raap M, Ließem S, Rüschoff J, Fisseler-Eckhoff A, Reiner A, Dirnhofer S, von Wasielewski R, Kreipe H

机构信息

Institute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.

Institute of Pathology Nordhessen, Kassel, Germany.

出版信息

Virchows Arch. 2017 Oct;471(4):501-508. doi: 10.1007/s00428-017-2142-y. Epub 2017 May 11.

Abstract

Ki67 is a broadly used proliferation marker in surgical pathology with an obvious need for standardization to improve reproducibility of assessment. Here, we present results of the so far only existing round robin tests on Ki67, organized annually in Germany, Austria, and Switzerland from 2010 to 2015 with up to 160 participating laboratories (QuIP). In each quality assessment trial, eight probes from each breast cancer, neuroendocrine tumor, and malignant lymphoma were compiled on a tissue microarray (TMA). TMAs were stained in the participants' laboratories with antibodies and procedures also applied in their daily routine. Participating pathologists were expected to assign Ki67 values to one of four different categories for each tumor type. All local stainings and evaluations were reassessed by the organizing panel and compared to a preset standard. On average, 95% of participants reached the benchmark of over 80% concordance rates with the Ki67 category pre-established by the panel. Automatization and type of antibody did not affect the success rate. Concordance rates differed between tumor entities being highest in each tumor type with either very high or very low labeling indices. Lower rates were seen for intermediate Ki67 levels. Staining quality improved during the observation period as did inter-observer concordance with 85% of participants achieving excellent agreement (kappa > 0.8) in the first year and over 95% in 2015. In conclusion, regular external quality assurance trials have been established as a tool to improve the reproducibility and reliability of the prognostic and predictive proliferation marker Ki67.

摘要

Ki67是外科病理学中广泛使用的增殖标志物,显然需要标准化以提高评估的可重复性。在此,我们展示了迄今为止仅有的关于Ki67的室间比对测试结果,该测试于2010年至2015年在德国、奥地利和瑞士每年组织一次,参与实验室多达160个(QuIP)。在每次质量评估试验中,从每例乳腺癌、神经内分泌肿瘤和恶性淋巴瘤中选取8个探针制作组织微阵列(TMA)。TMA在参与者的实验室中用抗体进行染色,染色程序也是他们日常工作中所使用的。参与的病理学家需要为每种肿瘤类型将Ki67值归入四个不同类别之一。所有局部染色和评估均由组织小组重新评估,并与预先设定的标准进行比较。平均而言,95%的参与者达到了与小组预先确定的Ki67类别一致性率超过80%的基准。自动化程度和抗体类型并不影响成功率。不同肿瘤实体的一致性率有所不同,在每种肿瘤类型中,标记指数非常高或非常低时一致性率最高。Ki67水平处于中等时一致性率较低。在观察期内,染色质量有所提高,观察者间的一致性也有所提高,2010年85%的参与者达到了优秀一致性(kappa>0.8),2015年这一比例超过了95%。总之,定期的外部质量保证试验已被确立为一种提高预后和预测增殖标志物Ki67的可重复性和可靠性的工具。

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