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Comparison of HER2 Dual-Color and Fluorescence In Situ Hybridization in Breast Cancer:  A Cohort Study Emphasizing Equivocal Cases.

乳腺癌中HER-2基因双色原位杂交和荧光原位杂交比较:重点关注不确定病例的队列研究

Shao T,Wood M,Wing A,Hnatovska M,Mendes M,Brendan Mullen J,Chang MC

Abstract

Human epidermal growth factor receptor 2 (HER2; ERBB2 gene) is of prognostic and predictive significance in breast carcinoma. Both fluorescence in situ hybridization (FISH) and dual-color in situ hybridization (DISH) methods are available. DISH and FISH are highly concordant in validation studies, but differences may be more prevalent in the equivocal range. Our goal was to compare FISH and DISH on a cohort enriched for equivocal cases, with respect to HER2 determination.
The cohort was enriched for equivocal (2+) cases. DISH and FISH were evaluated using standard protocols and the results compared with respect to HER2 status, HER2 copy number, and HER2/chromosome 17 (Chr17) ratio.
In total, 109 cases were identified. The agreement rate of DISH with FISH was 74%. The mean ± SD HER2/Chr17 ratio by DISH was 1.63 ± 0.08 vs 1.59 ± 0.26 by FISH (P = .45). The mean ± SD HER2 copy number by DISH was 4.56 ± 0.45 vs 4.75 ± 1.08 by FISH (P = .004). Individual signals were more easily resolved using FISH in cases with higher copy numbers.
In our cohort enriched for equivocal cases, the numerical values of HER2 copy number were significantly lower using DISH, resulting in discordances. Although DISH is a valid method, variations with FISH may be expected in high-equivocal cases and in quality assurance activities.

摘要

人表皮生长因子受体(HER2;ERBB2基因)对乳腺癌具有预后和预测的义。荧光原位杂交(FISH)和双色原位杂交(DISH)都可检测HER2基因。DISH和FISH在HER2基因的有效性研究中具有高度一致性,但在不确定性方面却有普遍差异。我们的目的是在不确定病例的队列中比较FISH和DISH检测HER2基因的情况。队列中有大量不确定(2+)例子。DISH和FISH检测用标准程序评估,从HER2状态、HER2拷贝数和HER2/17号染色体 (Chr17) 的比值方面比较这两种方法检测的结果。

总共检测109例,DISH和FISH的一致率是74%,两者检测的HER2/Chr17比值的平均值±标准差分别是1.63 ± 0.08(DISH)和1.59 ± 0.26(FISH)(P=0.45),HER2拷贝数的平均值±标准差分别是4.56 ± 0.45(DISH)及 4.75 ± 1.08( FISH )(P =0 .004)。高拷贝数的例子中单个信号用FISH方法更容易处理。这一具有大量不确定例子的队列中,DISH检测的HER2拷贝数显著降低从而产生了不一致。尽管DISH是有效的检测方法,但FISH检测更有望用于高度不确定的例子和质量控制中。

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