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乳腺癌组织芯片中Ki-67的表达:评估肿瘤异质性、与完整切片的一致性及评分方法

Ki-67 Expression in Breast Cancer Tissue Microarrays: Assessing Tumor Heterogeneity, Concordance With Full Section, and Scoring Methods.

作者信息

Khoury Thaer, Zirpoli Gary, Cohen Stephanie M, Geradts Joseph, Omilian Angela, Davis Warren, Bshara Wiam, Miller Ryan, Mathews Michelle M, Troester Melissa, Palmer Julie R, Ambrosone Christine B

机构信息

Department of Pathology.

Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, NY.

出版信息

Am J Clin Pathol. 2017 Aug 1;148(2):108-118. doi: 10.1093/ajcp/aqx053.

DOI:10.1093/ajcp/aqx053
PMID:28898983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5848430/
Abstract

OBJECTIVES

Ki-67 has been proposed to be used as a surrogate marker to differentiate luminal breast carcinomas (BCs). The purpose of this study was to determine the utility of and best approaches for using tissue microarrays (TMAs) and Ki-67 staining to distinguish luminal subtypes in large epidemiology studies of luminal/human epidermal growth factor receptor 2 (HER2)-negative BC.

METHODS

Full-section and TMA (three 0.6-mm cores and two 1.0-mm cores) slides of 109 cases were stained with Ki-67 antibody. We assessed two ways of collapsing TMA cores: a weighted approach and mitotically active approach.

RESULTS

For cases with at least a single 0.6-mm TMA core (n = 107), 16% were misclassified using a mitotically active approach and 11% using a weighted approach. For cases with at least a single 1.0-mm TMA core (n = 101), 5% were misclassified using either approach. For the 0.6-mm core group, there were 33.3% discordant cases. The number of discordant cases increased from 18% in the group of two cores to 40% in the group of three cores (P = .039).

CONCLUSIONS

Ki-67 tumor heterogeneity was common in luminal/HER2- BC. Using a weighted approach was better than using a mitotically active approach for core to case collapsing. At least a single 1.0-mm core or three 0.6-mm cores are required when designing a study using TMA.

摘要

目的

有人提出将Ki-67用作区分管腔型乳腺癌(BC)的替代标志物。本研究的目的是确定在管腔型/人表皮生长因子受体2(HER2)阴性BC的大型流行病学研究中,使用组织微阵列(TMA)和Ki-67染色来区分管腔亚型的实用性和最佳方法。

方法

用Ki-67抗体对109例病例的全切片和TMA(三个0.6毫米芯块和两个1.0毫米芯块)玻片进行染色。我们评估了两种将TMA芯块合并的方法:加权法和有丝分裂活跃法。

结果

对于至少有一个0.6毫米TMA芯块的病例(n = 107),使用有丝分裂活跃法时16%被错误分类,使用加权法时11%被错误分类。对于至少有一个1.0毫米TMA芯块的病例(n = 101),使用任何一种方法时5%被错误分类。对于0.6毫米芯块组,有33.3%的病例不一致。不一致病例的数量从两个芯块组的18%增加到三个芯块组的40%(P = .039)。

结论

Ki-67肿瘤异质性在管腔型/HER2阴性BC中很常见。在将芯块合并到病例时,使用加权法比使用有丝分裂活跃法更好。在设计使用TMA的研究时,至少需要一个1.0毫米芯块或三个0.6毫米芯块。

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