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Quality assessment of estrogen receptor and progesterone receptor testing in breast cancer using a tissue microarray-based approach

机译:使用基于组织芯片的方法评估乳腺癌中雌激素受体和孕激素受体的质量

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摘要

Assessing hormone receptor status is an essential part of the breast cancer diagnosis, as this biomarker greatly predicts response to hormonal treatment strategies. As such, hormone receptor testing laboratories are strongly encouraged to participate in external quality control schemes to achieve optimization of their immunohistochemical assays. Nine Dutch pathology departments provided tissue blocks containing invasive breast cancers which were all previously tested for estrogen receptor and/or progesterone receptor expression during routine practice. From these tissue blocks, tissue microarrays were constructed and tested for hormone receptor expression. When a discordant result was found between the local and TMA result, the original testing slide was revised and staining was repeated on a whole-tissue block. Sensitivity and specificity of individual laboratories for testing estrogen receptor expression were high, with an overall sensitivity of 99.7 and 95.4 %, respectively. Overall sensitivity and specificity of progesterone receptor testing were 94.8 and 92.6 %, respectively. Out of 96 discordant cases, 36 cases would have been concordant if the recommended cut-off value of 1 % instead of 10 % was followed. Overall sensitivity and specificity of estrogen and progesterone receptor testing were high among participating laboratories. Continued enrollment of laboratories into quality control schemes is essential for achieving and maintaining the highest standard of care for breast cancer patients.Electronic supplementary materialThe online version of this article (doi:10.1007/s10549-015-3444-x) contains supplementary material, which is available to authorized users.
机译:评估激素受体状态是乳腺癌诊断的重要组成部分,因为该生物标志物可以极大地预测对激素治疗策略的反应。因此,强烈建议激素受体测试实验室参加外部质量控制计划,以实现其免疫组织化学测定的优化。荷兰的9个病理科提供了含有浸润性乳腺癌的组织块,这些组织块先前均已在常规实践中接受过雌激素受体和/或孕激素受体表达的测试。从这些组织块中,构建组织微阵列并测试激素受体的表达。当发现局部结果与TMA结果不一致时,修改原始测试载玻片,并在全组织块上重复染色。各个实验室检测雌激素受体表达的敏感性和特异性很高,总体敏感性分别为99.7%和95.4%。孕激素受体检测的总体敏感性和特异性分别为94.8%和92.6%。在96个不一致的案例中,如果遵循建议的临界值1%而不是10%,则本来应该是36个案例。在参与研究的实验室中,雌激素和孕激素受体检测的总体敏感性和特异性很高。继续将实验室纳入质量控制体系对于实现和维持乳腺癌患者的最高护理标准至关重要。电子补充材料本文的在线版本(doi:10.1007 / s10549-015-3444-x)包含补充材料,其中适用于授权用户。

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